EGAS00000000001 WTCCC case-control study for Bipolar Disorder Other
1980-01-01
EGAS00000000002 WTCCC case-control study for Bipolar Disorder - Combined Controls Other
1980-01-01
EGAS00000000003 WTCCC case-control study for Coronary Artery Disease Other
1980-01-01
EGAS00000000004 WTCCC case-control study for Coronary Artery Disease - Combined Controls Other
1980-01-01
EGAS00000000005 WTCCC case-control study for Coronary Artery Disease, Hypertension, T2D - combined cases Other
1980-01-01
EGAS00000000006 Genomewide Association Study of Inflammatory Bowel Disease Other
1980-01-01
EGAS00000000007 Genomewide Association Study of Inflammatory Bowel Disease - Combined Controls Other
1980-01-01
EGAS00000000008 WTCCC case-control study for Inflammatory Bowel Disease, T1D and RA - combined cases Other
1980-01-01
EGAS00000000009 WTCCC case-control study for Hypertension Other
1980-01-01
EGAS00000000010 WTCCC case-control study for Hypertension - Combined Controls Other
1980-01-01
EGAS00000000011 WTCCC case-control study for Rheumatoid Arthritis Other
1980-01-01
EGAS00000000012 WTCCC case-control study for Rheumatoid Arthritis - Combined Controls Other
1980-01-01
EGAS00000000013 WTCCC case-control study for T1D and RA - combined cases Other
1980-01-01
EGAS00000000014 WTCCC case-control study for Type 1 Diabetes Other
1980-01-01
EGAS00000000015 WTCCC case-control study for Type 1 Diabetes - Combined Controls Other
1980-01-01
EGAS00000000016 WTCCC case-control study for Type 2 Diabetes Other
1980-01-01
EGAS00000000017 WTCCC case-control study for Type 2 Diabetes - Combined Controls Other
1980-01-01
EGAS00000000018 WTCCC case-control study for Ankylosing Spondylitis Other
1980-01-01
EGAS00000000019 WTCCC case-control study for Ankylosing Spondylitis - Combined Controls Other
1980-01-01
EGAS00000000020 WTCCC case-control study for Autoimmune Thyroid Disease Other
1980-01-01
EGAS00000000021 WTCCC case-control study for Autoimmune Thyroid Disease - Combined Controls Other
1980-01-01
EGAS00000000022 WTCCC case-control study for Multiple Sclerosis Other
1980-01-01
EGAS00000000023 WTCCC case-control study for Multiple Sclerosis - Combined controls Other
1980-01-01
EGAS00000000024 WTCCC case-control study for Breast cancer Other
1980-01-01
EGAS00000000025 WTCCC case-control study for Breast cancer - Combined Controls Other
1980-01-01
EGAS00000000026 MalariaGEN case-control study in the Gambia Other
1980-01-01
EGAS00000000027 WTCCC case-control study for Tuberculosis Other
1980-01-01
EGAS00000000028 WTCCC2 project controls - 1958 British Birth Cohort and National Blood Service Other
1980-01-01
EGAS00000000029 Massive Genomic Rearrangment Acquired in a Single Catastrophic Event During Cancer Development Whole Genome Sequencing
1980-01-01
EGAS00000000030 Nordic Samples on build 36 Other
1980-01-01
EGAS00000000031 HLA has strongest association with IgA nephropathy in genome-wide analysis Other
1980-01-01
EGAS00000000032 Control sets genotyped with Dynal RELI SSO and Roche Molecular Systems platfroms Other
1980-01-01
EGAS00000000033 Geographical structure and differential natural selection among North European populations Other
1980-01-01
EGAS00000000034
Genome-wide association scan in Parkinson's disease
Other
1980-01-01
EGAS00000000036 HLA-A*3101 and Carbamazepine-Induced Hypersensitivity Reactions in Europeans Other
1980-01-01
EGAS00000000037 Carbamazepine-induced hypersensitivity reactions in Europeans Other
1980-01-01
EGAS00000000038 T1DGC GWAS 1958 British Birth Cohort controls Other
1980-01-01
EGAS00000000039 WTCCC3 case-control study for Primary Biliary Cirrhosis Other
1980-01-01
EGAS00000000040 Mutation of FOXL2 in granulosa cell tumors of the ovary Whole Genome Sequencing
1980-01-01
EGAS00000000043 WNT-signaling and Dupuytren's Disease Other
1980-01-01
EGAS00000000048 A MITF germline mutation predisposes to melanoma and renal cell carcinoma Other
1980-01-01
EGAS00000000051 A small cell lung cancer genome reports complex tobacco exposure signatures Whole Genome Sequencing
1980-01-01
EGAS00000000052 A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome Whole Genome Sequencing
1980-01-01
EGAS00000000053 Coeliac Disease Immunochip dataset Other
1980-01-01
EGAS00000000054 Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution Whole Genome Sequencing
1980-01-01
EGAS00000000055 Procardis study on novel susceptibility genes for coronary artery disease (CAD) Other
1980-01-01
EGAS00000000056 Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts Other
1980-01-01
EGAS00000000057 Genome wide association study of Coeliac Disease Other
1980-01-01
EGAS00000000059 Assessment of genomic copy number alterations in breast cancer Cancer Genomics
1980-01-01
EGAS00000000060 A genome-wide meta analysis on stroke and ischemic stroke within four populations Other
1980-01-01
EGAS00000000062 Complex Landscapes of Somatic Rearrangements in Human Breast Cancer Genomes Whole Genome Sequencing
1980-01-01
EGAS00000000064 The patterns and dynamics of genomic instability in metastatic pancreatic cancer Whole Genome Sequencing
1980-01-01
EGAS00000000074 Evolution of an adenomacarcinoma in response to selection by targeted kinase inhibitors Other
1980-01-01
EGAS00000000075 ARID1A Mutations in Endometriosis-Associated Ovarian Carcinomas Other
1980-01-01
EGAS00000000077 A Large-Scale, Consortium-Based Genomewide Association Study of Asthma Other
1980-01-01
EGAS00000000082 ZNF703 is a common Luminal B breast cancer oncogene that differentially regulates luminal and basal progenitors in human mammary epithelium. Other
1980-01-01
EGAS00000000083 METABRIC Other
1980-01-01
EGAS00000000084 WTCCC2 case-control study for Ulcerative Colitis Other
1980-01-01
EGAS00000000086 An immune response network associated with blood lipid levels Other
1980-01-01
EGAS00000000087 Genome-wide association study of severe malaria in Gambian mother-father-child trios Other
1980-01-01
EGAS00000000088 Genome-wide association study of severe malaria in Ghanain mother-farther-child trios Other
1980-01-01
EGAS00000000092 CLL Genome Cancer Genomics
1980-01-01
EGAS00000000097 Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
Other
1980-01-01
EGAS00000000098 METABRIC Other
1980-01-01
EGAS00000000099 Identification of genetic etiology of CAMRQ2 Other
1980-01-01
EGAS00000000101 The Genetic Analysis of multiple sclerosis Other
1980-01-01
EGAS00000000102 Molecular Phenotyping to Accelerate Genomic Epidemiology (MolPAGE) Other
1980-01-01
EGAS00000000103 WTCCC2 Ischaemic Stroke study Other
1980-01-01
EGAS00000000104 Genomewide association studies in ankylosing spondylitis Other
1980-01-01
EGAS00000000105 Copy number analysis of Diamond-Blackfan Anemia (DBA) using SNP array Other
1980-01-01
EGAS00000000108 Genome-wide association scan in psoriasis Other
1980-01-01
EGAS00000000109 Genetics of gene expression in primary human immune cells
Other
1980-01-01
EGAS00000000114 Krakow experiment - Northern Finland Birth Cohort 1966 Other
1980-01-01
EGAS00000000115 Association studies using the Metabochip array - Samples analysed by the WTCCC (1958 British Birth Cohort (58BC), Hypertension cohort (HT), Type 2 Diabetes Cohort (T2D) and Coronary Artery Disease (CAD) cohort) Other
1980-01-01
EGAS00000000116 Molecular Sub-grouping of CNS-PNET Other
1980-01-01
EGAS00000000118 WTCCC2 Schizophrenia study Other
1980-01-01
EGAS00000000119 Powerful Identification of Cis-regulatory SNPs in Human Primary Monocytes Using Allele-Specific Gene Expression Other
1980-01-01
EGAS00000000121 WTCCC2 Pharmacogenomic Response to Statins study Other
1980-01-01
EGAS00000000122 METABRIC miRNA landscape Other
1980-01-01
EGAS00000000129 The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome Other
1980-01-01
EGAS00000000131 Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese Samples Other
1980-01-01
EGAS00000000132 The Haemgen RBC study Other
1980-01-01
EGAS00000000134 NOWAC blood-based breast cancer case-control study Other
1980-01-01
EGAS00000000135 Genome-wide differential DNA methylation signatures in pediatric acute
lymphoblastic leukemia Other
1980-01-01
EGAS00000000137 MRCA and MRCE SNP genotypes Other
1980-01-01
EGAS00001000001 Exome Resequencing of Progressive Hearing Loss Resequencing
2010-09-03
EGAS00001000002 Breast Cancer Follow Up Series Cancer Genomics
2010-09-08
EGAS00001000003 Cancer Single Cell Sequencing Other
2010-09-15
EGAS00001000004 Multifocal_Breast_Project Cancer Genomics
2010-10-13
EGAS00001000005 Lung_Rearrangement_Study Cancer Genomics
2010-10-15
EGAS00001000006 Renal_Cancer_Exome_Sequencing Cancer Genomics
2010-10-28
EGAS00001000008 Whole_Genome_Sequencing_of_hiPS_cells Whole Genome Sequencing
2010-11-04
EGAS00001000009 SCLC Synthetic Genomics
2010-11-10
EGAS00001000011 CLL_cancer_Sample_Sequencing Cancer Genomics
2010-11-17
EGAS00001000012 Various_Cancer_Fusion_Gene_Sequencing Cancer Genomics
2010-11-17
EGAS00001000013 Osteosarcoma_Sequencing Cancer Genomics
2010-11-17
EGAS00001000014 CLL_Cancer_Whole_Genome_Sequencing Cancer Genomics
2010-11-17
EGAS00001000016 The_GENCODE_exome___sequencing_the_complete_human_exome Exome Sequencing
2010-11-17
EGAS00001000017 Familial Melanoma Sequencing Exome Sequencing
2010-11-26
EGAS00001000020 Genetic_variation_in_Kuusamo Population Genomics
2011-01-04
EGAS00001000023 Identifying autosomal recessive mutations causing neurological disorders Other
2011-01-11
EGAS00001000024 Piloting exome resequencing in consanguineous families with homozygosity mapping intervals Other
2011-01-11
EGAS00001000025 Whole_exome_sequencing_of_Severe_Insulin_Resistant_patients_ Other
2011-01-12
EGAS00001000026 Whole_Exome_Sequencing_for_Characterization_of_Disease_Causing_Mutations_in_two_Pakistani_Families_Suffering_from_Autosomal_Recessive_Ocular_Disorders_ Other
2011-01-12
EGAS00001000027 TMD_AMLK_Exome_Study Cancer Genomics
2011-01-17
EGAS00001000028 PV_Exome_Study Cancer Genomics
2011-01-17
EGAS00001000030 ADCC_Rearrangement_Screen Cancer Genomics
2011-02-02
EGAS00001000031 Matched_breast_cancer_fusion_gene_study Cancer Genomics
2011-02-07
EGAS00001000032 Kaposi_sarcoma_exome Cancer Genomics
2011-02-07
EGAS00001000033 1__Fanconi_Anemia_transformation_to_AML Cancer Genomics
2011-02-14
EGAS00001000034 MDSMPN_Rearrangement_Screen Cancer Genomics
2011-02-14
EGAS00001000035 Sequencing_Acute_Myeloid_Leukaemia_ Synthetic Genomics
2011-02-18
EGAS00001000036 Integrative_Oncogenomics_of_Multiple_Myeloma Cancer Genomics
2011-03-01
EGAS00001000037 Gastric_and_Esophageal_tumour_rearrangement_screen Cancer Genomics
2011-03-03
EGAS00001000038 Chondrosarcoma_Exome_ Cancer Genomics
2011-03-15
EGAS00001000040 Exome sequencing of hyperplastic polyposis patients Other
2011-03-17
EGAS00001000041 Disorders_of_growth_and_insulin_action_ Other
2011-03-17
EGAS00001000042 HER2_positive_Breast_Cancer_ Cancer Genomics
2011-03-18
EGAS00001000043 Investigating_low_frequency_variants_in_CAD_MI_cases__controls_and_pedigrees_using_whole_exome_sequencing_and_custom_pulldowns Other
2011-03-22
EGAS00001000044 Identification_and_functional_validation_of_driver_mutations_in_colorectal_cancer Other
2011-03-23
EGAS00001000046 Mutational_Screening_of_Human_Acute_Myleloid_Leukaemia_Samples Other
2011-04-01
EGAS00001000047 Whole Exome Sequencing of Permanent Neonatal Diabetes Patients Other
2011-04-01
EGAS00001000048 Paroxysmal neurological disorders Other
2011-04-01
EGAS00001000049 Exome_sequencing_in_patients_with_Calcific_Aortic_Valve_Stenosis Other
2011-04-04
EGAS00001000050 Investigating_low_frequency_variants_in_CAD_MI_cases__controls_and_pedigrees_using_whole_exome_sequencing_and_custom_pulldowns Other
2011-04-04
EGAS00001000052 PAS Pedigrees: Identification of novel genetic variants contributing to cardiovascular disease in pedigrees with premature atherosclerosis. Other
2011-04-05
EGAS00001000053 Investigation of the genetic basis of the rare syndrome Post-Transfusion Purpura (PTP) Other
2011-04-05
EGAS00001000054 Identifying causative mutations for Thrombocytopenia with Absent Radii Other
2011-04-05
EGAS00001000055 Analysis_of_genomic_integrity_of_disease_corrected_human_induced_pluripotent_stem_cells_by_exome_sequencing Other
2011-04-05
EGAS00001000057 An exome sequencing pilot study of HIV elite-long term non progressors and rapid progressors Other
2011-04-12
EGAS00001000058 Acute_Lymphoblastic_Leukemia_Sequencing Cancer Genomics
2011-04-13
EGAS00001000059 De_novo_mutations_in_schizophrenia_ Other
2011-04-14
EGAS00001000060 Whole_genome_sequencing_in_a_multiplex_Crohn_s_disease_family Whole Genome Sequencing
2011-04-21
EGAS00001000061 Lethal malformation syndrome Other
2011-05-04
EGAS00001000062 The_International_1q_type_2_diabetes_consortium Other
2011-05-06
EGAS00001000063 Exome_sequencing_in_patients_with_cardiac_arrhythmias Other
2011-05-06
EGAS00001000064 Genetics of Microcephalic Osteodysplatics Primordial Dwarfism Other
2011-05-13
EGAS00001000065 Whole_genome_sequencing_of_Crohn_s_disease_patients Whole Genome Sequencing
2011-05-17
EGAS00001000066 Congenital Heart Disease in UK Families Other
2011-05-18
EGAS00001000067 Samples from the Greek island of Crete, MANOLIS cohort Whole Genome Sequencing
2011-05-19
EGAS00001000068 ORCADES_WGA Whole Genome Sequencing
2011-05-23
EGAS00001000069 Determination of the molecular nature of the Vel blood group by exome sequencing Other
2011-05-27
EGAS00001000070 Recurrent Somatic Mutations in CLL Cancer Genomics
2011-06-01
EGAS00001000071 Tetralogy of Fallot Exome Trios Other
2011-06-08
EGAS00001000074 Screening_for_human_epigenetic_variation_at_CpG_islands Epigenetics
2011-06-17
EGAS00001000075 Functional_characterisation_of_CpG_islands_in_human_and_mouse_tissues Epigenetics
2011-06-17
EGAS00001000076 Screening_for_abnormal_CGI_methylation_in_primary_colorectal_tumours Epigenetics
2011-06-17
EGAS00001000077 Human_Colorectal_Cancer_Exome_Sequencing Other
2011-06-23
EGAS00001000078 SFHS_pedigrees Whole Genome Sequencing
2011-06-23
EGAS00001000079 Cardiogenics_re_sequencing Resequencing
2011-06-24
EGAS00001000080 CRLF2_sequencing_project_ Cancer Genomics
2011-06-24
EGAS00001000081 CRLF2_sequencing_project_Exomes Cancer Genomics
2011-06-24
EGAS00001000082 ALK_inhibitors_in_the_context_of_ALK_dependent_cancer_cell_lines Cancer Genomics
2011-06-24
EGAS00001000083 CAGEKID: Cancer Genomics of the Kidney Cancer Genomics
2011-06-24
EGAS00001000085 Linking genes, genomic instability and molecular subgroups in medulloblastoma Whole Genome Sequencing
2011-06-30
EGAS00001000086 Dilgom_Exome Other
2011-06-30
EGAS00001000087 Burden_of_Disease_in_Sarcoma Cancer Genomics
2011-07-01
EGAS00001000088 Familial_Thrombocytosis_germline_exome_sequencing Cancer Genomics
2011-07-05
EGAS00001000089 Myelodysplastic_Syndrome_Exome_Sequnecing Other
2011-07-05
EGAS00001000090 UK10K COHORT ALSPAC Other
2011-07-13
EGAS00001000091 Grey_Platelet_Syndrome__GPS_ Other
2011-07-14
EGAS00001000092 Triple_Negative_Breast_Cancer_Whole_Genomes Cancer Genomics
2011-07-20
EGAS00001000093 Unraveling_the_genetic_basis_of_a_collagen_migration_defect_in_patients_with_a_combined__platelet_dysfunction_and_reduced_bone_density Other
2011-07-21
EGAS00001000094 PREDICT Cancer Genomics
2011-07-27
EGAS00001000095 Renal_Follow_Up_Series Cancer Genomics
2011-08-04
EGAS00001000096 Identification of improved IL28B SNPs and haplotypes for prediction of drug response in treatment of hepatitis C using massively parallel sequencing in a cross-sectional European cohort Resequencing
2011-08-05
EGAS00001000097 Chromatin_Profiling_in_Twins Gene Regulation Study
2011-08-09
EGAS00001000098 Chromatin_Profiling_in_Twins Gene Regulation Study
2011-08-09
EGAS00001000099 Exome_sequencing_of_a_Novel_Primary_T_Cell_Immunodeficiency_Kindred Other
2011-08-11
EGAS00001000100 Exome_Sequencing__to_Identify_Causes_of_Leukaemia_Predisposing_Congenital_Neutropenias Other
2011-08-11
EGAS00001000101 UK10K_RARE_NEUROMUSCULAR Other
2011-08-16
EGAS00001000102 ET_Exome Cancer Genomics
2011-08-17
EGAS00001000103 Genomics_of_Colorectal_Cancer_Metastases___Massively_Parallel_Sequencing_of_Matched_Primary_and_Metastatic_tumours_to_Identify_a_Metastatic_Signature_of_Somatic_Mutations__MOSAIC_ Cancer Genomics
2011-08-17
EGAS00001000104 Hyperfibrinolysis Other
2011-08-17
EGAS00001000105 Platelet_collagen_defect Other
2011-08-17
EGAS00001000106 Bleeding Other
2011-08-17
EGAS00001000107 Various_Platelet_Disorders Other
2011-08-17
EGAS00001000108 UK10K COHORT TWINSUK Other
2011-08-18
EGAS00001000109 UK10K NEURO ABERDEEN Other
2011-08-18
EGAS00001000110 UK10K_NEURO_ASD_FI Exome Sequencing
2011-08-18
EGAS00001000111 UK10K NEURO ASD BIONED Other
2011-08-18
EGAS00001000112 UK10K NEURO ASD GALLAGHER Exome Sequencing
2011-08-18
EGAS00001000113 UK10K NEURO ASD MGAS Other
2011-08-18
EGAS00001000114 UK10K NEURO ASD SKUSE Other
2011-08-18
EGAS00001000115 UK10K NEURO ASD TAMPERE Other
2011-08-18
EGAS00001000117 UK10K NEURO EDINBURGH Other
2011-08-18
EGAS00001000118 UK10K NEURO FSZ Other
2011-08-18
EGAS00001000119 UK10K NEURO FSZNK Other
2011-08-18
EGAS00001000120 UK10K NEURO IMGSAC Other
2011-08-18
EGAS00001000121 UK10K NEURO IOP COLLIER Other
2011-08-18
EGAS00001000122 UK10K_NEURO_MUIR Exome Sequencing
2011-08-18
EGAS00001000123 UK10K NEURO UKSCZ Exome Sequencing
2011-08-18
EGAS00001000124 UK10K_OBESITY_SCOOP Exome Sequencing
2011-08-18
EGAS00001000125 UK10K RARE CHD Other
2011-08-18
EGAS00001000126 UK10K_RARE_CILIOPATHIES Other
2011-08-18
EGAS00001000127 UK10K RARE COLOBOMA Other
2011-08-18
EGAS00001000128 UK10K_RARE_FIND Other
2011-08-18
EGAS00001000129 UK10K_RARE_HYPERCHOL Exome Sequencing
2011-08-18
EGAS00001000130 UK10K_RARE_SIR Other
2011-08-18
EGAS00001000131 UK10K_RARE_THYROID Exome Sequencing
2011-08-18
EGAS00001000132 The clonal and mutational evolution spectrum of primary triple negative breast cancers Exome Sequencing
2011-08-18
EGAS00001000133 Genetic_factors_underlying_premature_coronary_heart_disease_in_patients_with_normal_coronary_arteries Other
2011-08-22
EGAS00001000134 An_evaluation_of_different_strategies_for_large_scale_pooled_sequencing_study_design_ Resequencing
2011-08-25
EGAS00001000135 Recurrent somatic DICER1 mutations in non-epithelial ovarian tumors Cancer Genomics
2012-01-04
EGAS00001000136 'Targeted High Throughput Sequencing in Clinical Cancer Settings: Formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity' Resequencing
2011-09-01
EGAS00001000137 ENGAGE___Amendment__500_genes_exon_sequencing_ Other
2011-09-06
EGAS00001000138 Radiotherapy_induced_sarcoma Cancer Genomics
2011-09-08
EGAS00001000139 Splenic_Marginal_Zone_Lymphoma_with_villous_lymphocytes_exome_sequencing Cancer Genomics
2011-09-08
EGAS00001000140 Xenograft_Sequencing Cancer Genomics
2011-09-09
EGAS00001000142 Exome sequencing of patients with structural brain malformations Other
2011-09-20
EGAS00001000145 A_study_of_the_genetic_basis_of_evation_by_Acute_Myeloid_Leukaemia_of_Graft_vs_Leukaemia_effects_after_allogeneic_bone_marrow_transplantation Other
2011-09-21
EGAS00001000146 Exome_Sequencing_of_Poor_Prognosis_Acute_Myeloid_Leukaemia Other
2011-09-23
EGAS00001000147 Osteosarcoma_Whole_Genome Cancer Genomics
2011-09-23
EGAS00001000148 Lung_Cancer_Whole_Genomes Cancer Genomics
2011-09-27
EGAS00001000149 Whole-exome sequencing of human pancreatic cancers and characterization of genomic instability caused by MLH1 haploinsufficiency and complete deficiency Exome Sequencing
2011-09-30
EGAS00001000151 Exome_sequencing_Parkinson_s_disease_patients Other
2011-09-30
EGAS00001000152 Full genome sequencing of a monozygotic twin discordant for schizophrenia Whole Genome Sequencing
2011-10-03
EGAS00001000153 Exome Sequencing of Gastric Cancer Exome Sequencing
2011-10-04
EGAS00001000154 Genome Landscape of Primary Pancreatic Ductal Adenocarcinoma Other
2011-10-07
EGAS00001000155 Matched_Ovarian_Cancer_Sequencing Cancer Genomics
2011-10-13
EGAS00001000156 Otosclerosis_gene_discovery_ Other
2011-10-19
EGAS00001000157 Hearing_loss_in_adults_from_South_Carolina_ Other
2011-10-19
EGAS00001000158 Complete Genomics paired end sequencing; Ovarian cancer Whole Genome Sequencing
2011-10-20
EGAS00001000159 Exome sequencing of patients with rare neurological disorders Other
2011-10-25
EGAS00001000160 Matched_Pair_Cancer_Cell_line_Whole_Genomes Cancer Genomics
2011-10-25
EGAS00001000161 Triple_Negative_Breast_Cancer_sequencing Cancer Genomics
2011-10-27
EGAS00001000162 Genetic_background_for_the_major_psychiatric_disorders_in_the_general_Finnish_population Whole Genome Sequencing
2011-11-02
EGAS00001000163 Osteosarcoma_Exome_Sequencing Cancer Genomics
2011-11-02
EGAS00001000164 ESGI___Molecular_diagnosis_for_mitochondrial_disorders_ Other
2011-11-04
EGAS00001000165 Monotherapy_Breast_Cancer Cancer Genomics
2011-11-14
EGAS00001000166 Breast_Cancer_Matched_Pair_Cell_Line_Whole_Genomes Cancer Genomics
2011-11-14
EGAS00001000167 Abnormal_foetal_development_exome_trios Other
2011-11-15
EGAS00001000169 Whole genome sequencing of matched primary and metastatic acral melanomas Cancer Genomics
2011-11-29
EGAS00001000170 20_Matched_Pair_Breast_Cancer_Genomes Cancer Genomics
2011-11-29
EGAS00001000171 Exome_sequencing_of_blastic_plasmacytoid_dendritic_cell_neoplasms Other
2011-11-30
EGAS00001000172 BRAF_and_MEK_resistant_cell_line_clones Cancer Genomics
2011-11-30
EGAS00001000173 Testing_the_feasibility_of_genome_scale_sequencing_in_routinely_collected_FFPE_cancer_specimens_versus_matched_fresh_frozen_samples Cancer Genomics
2011-11-30
EGAS00001000174 Balanced_Ependymoma Cancer Genomics
2011-11-30
EGAS00001000175 PMF_Exome_Study Cancer Genomics
2011-11-30
EGAS00001000176 FRCC_Exome_sequencing Cancer Genomics
2011-11-30
EGAS00001000177 Meningioma_Exome Cancer Genomics
2011-11-30
EGAS00001000178 Cell_Line_Sub_Clone_Rearrangement_Screen Cancer Genomics
2011-11-30
EGAS00001000179 Renal_Matched_Pair_Cell_Line_Exome_Sequencing Cancer Genomics
2011-11-30
EGAS00001000180 Mixed_Leukemia_Rearrangement_Screen Cancer Genomics
2011-11-30
EGAS00001000181 Chondrosarcoma_Validation_Study Cancer Genomics
2011-11-30
EGAS00001000182 Signatures of mismatch repair deficiency in cancer genomes Whole Genome Sequencing
2011-12-05
EGAS00001000185 Exome_sequencing_of_Congenital_Heart_Disease_families_Leuven Other
2011-12-09
EGAS00001000187 Exome_sequencing_of_Congenital_Heart_Disease_families_Royal_Brompton Other
2011-12-09
EGAS00001000188 Chordoma_Exome_Sequencing Cancer Genomics
2011-12-14
EGAS00001000189 Dyslipidemia Other
2011-12-19
EGAS00001000190 Paroxysmal_Neurological_Disorders_2 Other
2012-01-03
EGAS00001000191 CML_blast_phase_rearrangement_screen Cancer Genomics
2011-08-26
EGAS00001000192 Somatic Histone H3 Mutations in Diffuse Intrinsic Pontine Gliomas and Non-Brainstem Paediatric Glioblastomas Whole Genome Sequencing
2012-01-04
EGAS00001000193 ADCC_Exome_Sequencing Cancer Genomics
2012-01-09
EGAS00001000194 Radiotherapy_induced_Sarcoma_exome Cancer Genomics
2012-01-09
EGAS00001000195 Breast_Cancer_Somatic_Genetics_Study_ Cancer Genomics
2012-01-10
EGAS00001000196 SCAT_osteosarcoma_sequencing Cancer Genomics
2012-01-12
EGAS00001000197 ER___HER2___PR__breast_Cancer_genome_sequencing Cancer Genomics
2012-01-12
EGAS00001000198 Myeloproliferative_Disorder_Sequencing Cancer Genomics
2012-01-12
EGAS00001000199 Myeloproliferative_Disorder_Sequencing Cancer Genomics
2012-01-12
EGAS00001000200 Acute_Lymphoblastic_Leukemia_Exome_sequencing_2_ Cancer Genomics
2012-01-12
EGAS00001000201 Acute_Lymphoblastic_Leukemia_Exome_sequencing Cancer Genomics
2012-01-12
EGAS00001000202 Glioma_cell_lines_rearrangement_screen Cancer Genomics
2012-01-12
EGAS00001000203 ChIP_sequencing_in_Cancer_Cell_Lines Cancer Genomics
2012-01-12
EGAS00001000205 Non_Tumour_Renal_Cell_Line_Sequencing Cancer Genomics
2012-01-12
EGAS00001000206 Cancer_Exome_Resequencing Cancer Genomics
2012-01-12
EGAS00001000207 Breast_Cancer_Exome_Resequencing Cancer Genomics
2012-01-12
EGAS00001000208 Cancer_Genome_Libraries_Tests Whole Genome Sequencing
2012-01-12
EGAS00001000209 Acute_Myeloid_Leukemia_Sequencing Cancer Genomics
2012-01-12
EGAS00001000210 Breast_Cancer_Whole_Genome_Sequencing Cancer Genomics
2012-01-13
EGAS00001000211 Breast_Cancer_Exome_Sequencing Cancer Genomics
2012-01-13
EGAS00001000212 MuTHER_adipose_tissue_small_RNA_expression Transcriptome Analysis
2012-01-13
EGAS00001000213 Association of Age at Diagnosis and Genetic Mutations in Patients with Neuroblastoma Whole Genome Sequencing
2012-01-25
EGAS00001000214 Test_of_PCR_library_method_on_whole_genmoe_samples Cancer Genomics
2012-01-27
EGAS00001000215 ICGC PedBrain: Deep-sequencing of childhood brain tumors. Whole Genome Sequencing
2012-01-27
EGAS00001000216 Melanoma_TIL_Study_Exomes Other
2012-01-31
EGAS00001000217 Exome-sequencing identifies new oncogenes and tumor suppressor genes recurrently altered in hepatocellular carcinoma Exome Sequencing
2012-02-01
EGAS00001000218 CML_Discovery_Project Cancer Genomics
2012-02-01
EGAS00001000220 Identifying_Novel_Fusion_Genes_in_Myeloma Cancer Genomics
2012-02-03
EGAS00001000222 Whole Genome Sequencing of Neuroblastoma Whole Genome Sequencing
2012-02-03
EGAS00001000224 Myelodysplastic_Syndrome_Follow_Up_Series Cancer Genomics
2012-02-06
EGAS00001000225 UK10K NEURO GURLING Other
2012-02-10
EGAS00001000226 Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma Cancer Genomics
2012-02-10
EGAS00001000228 Whole_exome_sequencing_of_rare_autoimmune_related_phenotypes Other
2012-02-13
EGAS00001000229 Genetic_background_for_cardio_vascular_disorders_in_the_general_Finnish_population Whole Genome Sequencing
2012-02-13
EGAS00001000230 RNAseq_Pulldown_ Other
2012-02-14
EGAS00001000231 Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells Whole Genome Sequencing
2012-02-15
EGAS00001000233 Pulldown_cytosine_deaminases Cancer Genomics
2012-02-24
EGAS00001000237 Ethiopia_Genome_Project__high_coverage_ Whole Genome Sequencing
2012-03-01
EGAS00001000238 Ethiopia_Genome_Project__low_coverage_ Whole Genome Sequencing
2012-03-01
EGAS00001000240 Whole_Exome_sequencing_in_a_large_IBD_pedigree Other
2012-03-01
EGAS00001000242 UK10K_OBESITY_GS Other
2012-03-01
EGAS00001000243 Integrative_Oncogenomics_of_multiple_myeloma Other
2012-03-12
EGAS00001000244 Integrative_Oncogenomics_of_multiple_myeloma Other
2012-03-12
EGAS00001000245 A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome Cancer Genomics
2012-03-13
EGAS00001000246 Genetic landscape of pediatric Infant Acute Lymphoblastic leukemia Whole Genome Sequencing
2012-03-14
EGAS00001000249 Genomic Alterations in Gingivo-buccal Cancer: ICGC-India Project_YR01 Other
2012-03-16
EGAS00001000250 Poikiloderma_syndrome_RNAseq Cancer Genomics
2012-03-16
EGAS00001000251 Melanoma_Til_Study_RNAseq Cancer Genomics
2012-03-16
EGAS00001000252 Whole_genome_sequencing_of_Italian_genetic_isolates__Friuli_Venezia_Giulia Whole Genome Sequencing
2012-03-16
EGAS00001000253 Whole genome sequencing of pediatric BCR-ABL1 positive acute lymphoblastic leukemia Whole Genome Sequencing
2012-03-20
EGAS00001000254 Genetic landscape of pediatric ependymoma Whole Genome Sequencing
2012-03-20
EGAS00001000255 Genetic landscape of pediatric Low Grade Gliomas & Glioneuronal tumors Whole Genome Sequencing
2012-03-20
EGAS00001000256 Genetic landscape of pediatric Rhabdomyosarcoma Other
2012-03-20
EGAS00001000257 Genetic landscape of pediatric Adrenocortical Tumor Other
2012-03-20
EGAS00001000260 Targeted_Pulldown_Validation_of_mutations_found_in_whole_genome_sequencing Cancer Genomics
2012-03-22
EGAS00001000261 Transcriptome_Sequencing_of_Cancer_Cell_Lines Cancer Genomics
2012-03-22
EGAS00001000262 CRUK-ICGC Prostate Cancer Group Study Other
2012-03-23
EGAS00001000263 Genetic landscape of pediatric Osteosarcoma Whole Genome Sequencing
2012-03-26
EGAS00001000264 Shwachman_Diamond_syndrome__SDS___Exome_sequencing Other
2012-03-26
EGAS00001000266 Exome_sequencing_of_patients_with_Ewings_sarcoma_ Other
2012-03-26
EGAS00001000267 RNAseq_of_patients_with_Ewings_sarcoma Cancer Genomics
2012-03-26
EGAS00001000268 Accurate mutation detection in leukemia by re-sequencing a cancer gene set Resequencing
2012-03-29
EGAS00001000269 Identification_of_the_underlying_causal_variant_in_a_multi_generational_family_with_autosomal_dominant_common_variable_immunodeficiency Other
2012-03-29
EGAS00001000271 Comparing sequencing of four proto-typical Burkitt lymphomas (BL) with IG-MYC translocation. Whole Genome Sequencing
2012-04-17
EGAS00001000272 Whole Genome Methylation in CLL Epigenetics
2012-04-17
EGAS00001000273 Stratifying and Targeting Pediatric Medulloblastoma through Genomics Other
2012-04-20
EGAS00001000274 Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies Whole Genome Sequencing
2012-04-23
EGAS00001000275 AML_targeted_resequencing_study Cancer Genomics
2012-04-25
EGAS00001000276 Genetic_mechanisms_of_resistance_to_chemotherapy_in_breast_cancer Other
2012-04-26
EGAS00001000277 Chondrosarcoma_Targeted_Sequencing_Study Cancer Genomics
2012-05-01
EGAS00001000278 Osteosarcoma_Targeted_Sequencing_Study Cancer Genomics
2012-05-02
EGAS00001000280 Chordoma_Targeted_Sequencing_Study Cancer Genomics
2012-05-02
EGAS00001000282 Meningioma_Targeted_Sequencing_Study Cancer Genomics
2012-05-02
EGAS00001000283 RNA_Seq_in_Patients_with_Primordial_Dwarfism Transcriptome Analysis
2012-05-15
EGAS00001000284 BLUEPRINT RNA-seq data for rare cells in the haematopoietic lineages, from adult and cord blood samples. Transcriptome Analysis
2012-05-29
EGAS00001000285 Validation_of_a_Haloplex_platform_for_targeted_re_sequencing_of_the_exons_of_25_genes Resequencing
2012-05-30
EGAS00001000286 APCDR AGV Project: WGS of South African Zulu Other
2012-05-30
EGAS00001000287 Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability Exome Sequencing
2012-05-30
EGAS00001000288 Genentech Colon Cancer Screen Cancer Genomics
2012-05-31
EGAS00001000289 Lung_Plasma_rearrangement_screen Cancer Genomics
2012-06-08
EGAS00001000290 Myeloproliferative_Disease_Whole_Genomes Cancer Genomics
2012-06-08
EGAS00001000291 Myelodysplastic_syndrome_whole_genomes Cancer Genomics
2012-06-08
EGAS00001000292 Molecular_characterization_of_invasive_lobular_carcinoma Cancer Genomics
2012-06-15
EGAS00001000293 Evaluation_of_size_selection_on_cancer_specific_sequencing_libraries Cancer Genomics
2012-06-15
EGAS00001000295 Gene_Discovery_in_Age_Related_Hearing_Loss Other
2012-06-18
EGAS00001000296 Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia Exome Sequencing
2012-06-18
EGAS00001000297 Feasibility_of_targeted_capture_sequencing_in_routinely_collected_FFPE_cancer_specimens Cancer Genomics
2012-06-18
EGAS00001000299 Integrative analysis of small cell lung cancer Other
2012-06-20
EGAS00001000300 Breast_cancer_sequential_sampling_study Cancer Genomics
2012-06-21
EGAS00001000301 Cancer_Genome_Project_Exome_Sequencing Other
2012-06-21
EGAS00001000305 P647_Targeted_resequencing_project Whole Genome Sequencing
2012-06-26
EGAS00001000306 UK10K OBESITY TWINSUK Other
2012-06-26
EGAS00001000308 Targeted_sequencing_of_candidate_genes_in_calcific_aortic_valve_stenosis Other
2012-06-27
EGAS00001000310 RNA_sequencing Other
2012-06-28
EGAS00001000315 Human_Evolution_3 Whole Genome Sequencing
2012-07-10
EGAS00001000317 Exome_sequencing_of_Congenital_Heart_Disease_families_Toronto Other
2012-07-17
EGAS00001000318 Whole-exome Sequencing Combined with Functional Genomics Reveals Novel Candidate Driver Cancer Genes in Endometrial Cancer Exome Sequencing
2012-07-17
EGAS00001000322 De_novo_mutations_in_cell_free_foetal_DNA__cffDNA_ Whole Genome Sequencing
2012-07-19
EGAS00001000323 Identifying genetic consequences of Epstein-Barr Virus transformation by comparing an individual’s genomic DNA with that of its lymphoblastoid cell line. Whole Genome Sequencing
2012-07-19
EGAS00001000326 BLUEPRINT ChIP-seq data for cells in the haematopoietic lineages, from adult and cord blood samples. Epigenetics
2012-08-01
EGAS00001000327 BLUEPRINT RNA-seq data for common cells in the haematopoietic lineages, from adult and cord blood samples. Transcriptome Analysis
2012-08-01
EGAS00001000328 Sequencing and analysis of a South Asian-Indian personal genome Whole Genome Sequencing
2012-08-08
EGAS00001000329 Identification_of_low_frequency_variants_associated_with_ulcerative_colitis_using_whole_genome_sequencing Whole Genome Sequencing
2012-08-09
EGAS00001000330 Osteosarcoma_whole_genome_rearrangement_screen Cancer Genomics
2012-08-09
EGAS00001000332 Helleday_HRAS_Project Cancer Genomics
2012-08-09
EGAS00001000333 Multiple_Malignancy_Familial_Comparison Cancer Genomics
2012-08-09
EGAS00001000334 Genentech Small Cell Lung Cancer (SCLC) Screen Other
2012-08-09
EGAS00001000335 A_study_of_the_molecular_pathogenesis_of_Splenic_Marginal_Zone_and_Diffuse_Large_B_Cell_Lymphoma Other
2012-08-10
EGAS00001000336 Understanding_population_genetics_and_patterns_of_genome_wide_heterozygosity_in_a_sample_of_the_Croatian_isolated_populations__ESGIDalmatians_ Other
2012-08-13
EGAS00001000337 Inferring tumor genomes from peripheral blood i.e. CTCs and plasma-DNA using deep sequencing and targeted enrichment Cancer Genomics
2012-08-14
EGAS00001000343 Pancreatic Cancer Sequencing Initiative Exome Sequencing
2012-08-22
EGAS00001000344 Exome_sequencing_of_thyroid_disease_in_Val_Borbera Other
2012-08-23
EGAS00001000346 Genetic landscape of pediatric Retinoblastoma Whole Genome Sequencing
2012-08-24
EGAS00001000347 Genetic landscape of pediatric Medulloblastoma Whole Genome Sequencing
2012-08-24
EGAS00001000348 Genetic landscape of Early T-cell precursor acute lymphoblastic leukaemia Whole Genome Sequencing
2012-08-24
EGAS00001000349 The Genomic Landscape of Core-Binding Factor Acute Myeloid Leukemias Other
2012-08-24
EGAS00001000351 BLUEPRINT DNase accessibility (NCMLS) Epigenetics
2012-08-28
EGAS00001000352 Epilepsy_related_sudden_death Other
2012-08-29
EGAS00001000353 The_genomic_architecture_of_mesothelioma_ Cancer Genomics
2012-08-31
EGAS00001000354 Primary_Lung_Cancer_whole_genome_study Cancer Genomics
2012-08-31
EGAS00001000356 Exome_sequencing_of_Bilateral_Anophthalmia_cases__Pilot_Study_ Other
2012-09-04
EGAS00001000358 Sequencing_the_exome_of_12_early_sporadic_human_colorectal_cancers__CRC_ Other
2012-09-05
EGAS00001000359 Mutation_analysis_in_human_iPS_cells_ Resequencing
2012-09-05
EGAS00001000360 Balanced_Brain_Tumour_Whole_Genome_Sequencing Cancer Genomics
2012-09-07
EGAS00001000362 Ewings_Sarcoma_Rearrangement_Screen Cancer Genomics
2012-09-07
EGAS00001000363 APCDR AGV Project: WGS of an Ugandan population Other
2012-09-13
EGAS00001000367 Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells_RNA Other
2012-10-02
EGAS00001000368 Exome_sequencing_of_Congenital_Heart_Disease_families_from_the_Competence_Network_Berlin Other
2012-10-05
EGAS00001000369 Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma Other
2012-10-08
EGAS00001000370 Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single nucleotide variants and tumoral heterogeneity by massively parallel sequencing Cancer Genomics
2012-10-08
EGAS00001000371 Whole-exome study to identify the causative germline mutations of congenital macrothrombocytopenia Exome Sequencing
2012-10-09
EGAS00001000373 Deep_sequencing_analysis_of_human_iPSC_specific_SNVs_in_donor_cell_population Resequencing
2012-10-11
EGAS00001000374 Deep RNA sequencing in CLL Other
2012-10-11
EGAS00001000377 Triple_Negative_Breast_Cancer_RNA_Sequencing Cancer Genomics
2012-10-18
EGAS00001000379 Genetic landscape of non-Down syndrome acute megkaryoblastic leukemia Whole Genome Sequencing
2012-10-19
EGAS00001000380 GEenetic landscape of hypodiploid acute lymphoblastic leukemia Whole Genome Sequencing
2012-10-19
EGAS00001000381 Whole-genome sequencing analysis of low-grade astrocytomas within the ICGC PedBrain Tumor Project Whole Genome Sequencing
2012-10-22
EGAS00001000382 Transcriptional_profiling_of_tauopathies_in_human_IPS_derived_neurons Transcriptome Analysis
2012-10-23
EGAS00001000383 The genomic landscape of large and small tumors in early-onset prostate cancer patients Cancer Genomics
2012-10-24
EGAS00001000384 Oulu_Dyslipidemia_families Other
2012-10-25
EGAS00001000385 Crohn_s_Exome_Sequencing Other
2012-10-25
EGAS00001000386 Paroxysmal_neurological_Disorders Other
2012-10-29
EGAS00001000387 Susceptibility_genes_for_the_development_of_SLE_during_treatment_of_IBD Other
2012-10-29
EGAS00001000388 Whole_exome_sequencing_of_young_onset_Primary_Sclerosing_Cholangitis Other
2012-10-29
EGAS00001000389 Whole exome sequencing of virus-associated HCC Exome Sequencing
2012-10-31
EGAS00001000390 Targeted_gene_fusion_sequencing__Fus_seq__in_mesothelioma Cancer Genomics
2012-10-31
EGAS00001000392 Low_coverage_whole_genome_sequencing_of_samples_from_the__Cretan_Greek_isolate_collection_HELIC_MANOLIS Whole Genome Sequencing
2012-11-01
EGAS00001000393 Whole-genome-Sequencing of adult medulloblastoma Whole Genome Sequencing
2012-11-07
EGAS00001000394 Genome-wide mutation analysis of germinal-center B-cell derived lymphomas within the ICGC MMML-Seq Consortium Other
2012-11-08
EGAS00001000395 Pancreatic Cancer Sequencing Initiative OICR Cancer Genomics
2012-11-19
EGAS00001000397 Genome Landscape of High-Grade Serous Ovarian Cancer Other
2012-11-27
EGAS00001000398 High_powered_complex_trait_association_mapping_through_whole_genome_sequencing_of_a_selected_subpopulation_of_the_INGI_Val_Borbera_genetic_isolate Whole Genome Sequencing
2012-11-30
EGAS00001000399 Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma. Whole Genome Sequencing
2012-12-02
EGAS00001000400 Integrative genomic analyses reveal androgen-driven somatic alteration landscape in early-onset prostate cancer Other
2012-12-04
EGAS00001000402 Feasibility_of_targeted_capture_sequencing_in_FFPE_cancer_specimens_2 Cancer Genomics
2012-12-06
EGAS00001000403 BASIS_Genome_Validation_Study Cancer Genomics
2012-12-14
EGAS00001000404 Myeloproliferative_Neoplasms__MPN__Exome_Validation_Study Cancer Genomics
2012-12-14
EGAS00001000405 Angiosarcoma_follow_up_study Cancer Genomics
2012-12-14
EGAS00001000406 Myeloproliferative_Neoplasms__MPN__Targeted_Gene_Screen Cancer Genomics
2012-12-14
EGAS00001000407 Characterization_of_individual_foci_of_multicentric_multifocal_breast_cancer_using_targeted_next_generation_sequencing Cancer Genomics
2012-12-14
EGAS00001000408 Targeted_sequencing_of_genes_recurrently_mutated_in_AML Cancer Genomics
2012-12-14
EGAS00001000409 Chordoma_Sequencing_Project_Whole_Genome Cancer Genomics
2012-12-14
EGAS00001000410 Chordoma_Sequencing_Project_RNAseq Cancer Genomics
2012-12-14
EGAS00001000411 The Cardiogenics study Transcriptome Analysis
2013-01-07
EGAS00001000413 The_Transcriptome_of_PLX4032_resistance Transcriptome Analysis
2013-01-15
EGAS00001000415 Analysis_of_resistance_to_PLX4032 Other
2013-01-17
EGAS00001000416 Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Uzbeks (DNA samples from the Institute of Immunology, Uzbek Academy of Sciences, Tashkent, Uzbekistan; Republic Specialized Scientific Practical Medical Centre of Obstetrics and Gynecology, Tashkent, Uzbekistan) Other
2013-01-21
EGAS00001000417 Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Kazakhs (DNA samples from the Scientific Center of Obstetrics, Gynecology and Perinatology, Almaty, Kazakhstan; Gulnara Svyatova, Principal Investigator Other
2013-01-21
EGAS00001000418 BLUEPRINT Bisulfite-seq (CNAG) Epigenetics
2013-01-22
EGAS00001000419 Ewings_Sarcoma_RNA_seq_drug_sensitivity Cancer Genomics
2013-01-28
EGAS00001000420 Breast_Cancer_FRT_RNA_seq Cancer Genomics
2013-01-28
EGAS00001000421 Paroxysmal_Neurological_Disorders___rare_epilepsies Other
2013-01-30
EGAS00001000423 Validation_of_Exome_sequencing_of_S7RE_iPSC_lines Resequencing
2013-02-01
EGAS00001000425 Congenital_Heart_Disease___Pilot Other
2013-02-04
EGAS00001000426 Triple_Negative_Breast_Cancer_Whole_Genome_Validations Cancer Genomics
2013-02-05
EGAS00001000427 Prostate_Cancer_Whole_Genome_Validations Cancer Genomics
2013-02-05
EGAS00001000428 Neoadjuvant_Breast_Cancer_Validations Cancer Genomics
2013-02-05
EGAS00001000429 Whole_genome_sequence_of__third_generation_family_member__SFHS_ Whole Genome Sequencing
2013-02-06
EGAS00001000430 Validation_of_AML_Mutational_Screening Resequencing
2013-02-13
EGAS00001000433 ICGC_Benchmarking_Exercise Whole Genome Sequencing
2013-02-15
EGAS00001000434 Matched_Pair_Cell_Line_Tumour_RNAseq Cancer Genomics
2013-02-15
EGAS00001000435 Single_Cell_Targeted_Sequence_Capture Cancer Genomics
2013-02-15
EGAS00001000436 Lung_Multi_site_Targeted_Sequence_Capture Cancer Genomics
2013-02-15
EGAS00001000437 Deep_sequencing_of_S7EPC_genome Resequencing
2013-02-18
EGAS00001000439 Noninvasive prenatal molecular karyotyping from maternal plasma Resequencing
2013-02-22
EGAS00001000441 Subclonal_analysis_in_S7RE2_and_S7RE14_iPS_cells Resequencing
2013-02-25
EGAS00001000442 Cell-type, allelic and genetic signatures in the human pancreatic beta cell transcriptome Transcriptome Analysis
2013-02-27
EGAS00001000443 Epigenomic alterations define lethal CIMP-positive ependymomas of infancy Other
2013-02-28
EGAS00001000446 Passive and active DNA methylation and the interplay with genetic variation in gene regulation Population Genomics
2013-03-07
EGAS00001000447 Germline Aberrations of PAX5 Cause Susceptibility to pre-B cell Acute Lymphoblastic Leukemia Exome Sequencing
2013-03-11
EGAS00001000449 The landscape of somatic mutations in epigenetic regulators across 1000 pediatric cancer genomes Epigenetics
2013-03-12
EGAS00001000451 Plasma-Seq of patients with metastatic prostate cancer Other
2013-03-13
EGAS00001000453 Identification of mutations and structural rearrangements in plasma DNA form metastatic prostate cancer patients Resequencing
2013-03-13
EGAS00001000455 Whole genome bisufite sequencing of smoking and non-smoking mother-child pairsBisufite sequencing, RNA-seq and ChIP-Seq data of whole blood samples from smoking and non-smoking mothers and their children at gestation/birth and follow-up years. Epigenetics
2013-03-15
EGAS00001000458 Whole_Genome_sequencing_of_individuals_from_Val_Borbera__Italy Whole Genome Sequencing
2013-03-20
EGAS00001000460 Whole_Genome_sequencing_of_individuals_from_Carlantino__Italy Whole Genome Sequencing
2013-03-20
EGAS00001000462 Autozygosity_pilot_Born_in_Bradford Other
2013-03-21
EGAS00001000464 Validation_of_SNVs_found_by_Exome_seq_in_S2_SF1___SF5_and__SF9_hiPSCs Resequencing
2013-03-25
EGAS00001000466 FFPE_CPA_Accreditation_Study Cancer Genomics
2013-03-26
EGAS00001000468 Harnessing_transposons_for_drug_resistance_gene_discovery_in_cancer Cancer Genomics
2013-03-26
EGAS00001000470 CMF_RNA_sequencing Cancer Genomics
2013-03-26
EGAS00001000472 Whole genome sequencing, SNP array and RNA-seq of uveal melanomas Other
2013-03-27
EGAS00001000474 Whole genome sequencing and whole exome sequencing of mucosal melanoma Other
2013-03-27
EGAS00001000476 Negligible impact on missing heritability of autoimmune-locus rare coding-region variants Resequencing
2013-04-04
EGAS00001000478 Genetic_factors_underlying_premature_MI_in_Greek_families_without_vessel_disease Other
2013-04-05
EGAS00001000480 Egypt_Genome_Project___low_coverage_whole_genome_sequencing Whole Genome Sequencing
2013-04-09
EGAS00001000482 Egypt_Genome_Project___high_coverage_whole_genome_sequencing Whole Genome Sequencing
2013-04-09
EGAS00001000484 Whole genome and transcriptome analysis of a sporadic and recurring parathyroid carcinoma Whole Genome Sequencing
2013-04-09
EGAS00001000486 Whole genome sequencing of acral melanomas Other
2013-04-12
EGAS00001000488 Sequencing_probands_and_families_with_severe_insulin_resistance_syndromes Other
2013-04-17
EGAS00001000490 Sequencing_component_for_the_whole_genome_methylation_analysis_in_PBMCs_and_cell_subsets__pilot_study_ Epigenetics
2013-04-22
EGAS00001000492 Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells Other
2013-04-23
EGAS00001000495 RNA Editing in breast cancer Transcriptome Analysis
2013-04-23
EGAS00001000501 Bone_Cancer___Rare_Types_Whole_Genome Cancer Genomics
2013-05-01
EGAS00001000505 Whole genome sequencing of chondrosarcoma Whole Genome Sequencing
2013-05-08
EGAS00001000506 Comprehensive analysis of atypical teratoid rhabdoid tumour (ATRT) using genomic, epigenomic and transcriptomic techniques. Other
2013-05-08
EGAS00001000509 an integrated molecular study of clear cell renal cell carcinoma (ccRCC) including whole-genome/exome and RNA sequencing as well as array-based gene expression/copy-number/methylation analyses Cancer Genomics
2013-05-13
EGAS00001000510 Landscape of somatic mutations and clonal evolution in mantle cell lymphoma Whole Genome Sequencing
2013-05-13
EGAS00001000511 Autozygosity_pilot___Pakistani_from_Birmingham Cancer Genomics
2013-05-15
EGAS00001000513 COLORS_in_IBD__Whole_exome_sequencing_of_early_onset_IBD_patients Other
2013-05-20
EGAS00001000514 ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA Whole Genome Sequencing
2013-05-20
EGAS00001000515 Use_of_Deep_Sequencing_to_Dectect_Clonal_Mutations_In_Sun_Exposed_Skin_Epidermis Cancer Genomics
2013-05-22
EGAS00001000518 Angiosarcoma_follow_up_2_validation_study Cancer Genomics
2013-05-24
EGAS00001000520 Cloning_of_the_breakpoint_of_a_novel_translocation_associated_with_T_acute_lymphoblastic_leukaemia Cancer Genomics
2013-05-24
EGAS00001000521 Whole exome and whole genome sequencing of juvenile myelomonocytic leukemia (JMML) Other
2013-05-24
EGAS00001000522 An_exome_sequencing_study_of_the_HIV_elite_long_term_non_progressors_and_rapid_progressors__CASCADE_cohorts_ Other
2013-05-28
EGAS00001000523 ESGI_Identification_of_novel_genes_and_mechanisms_leading_to_Primary_Ciliary_Dyskinesia Other
2013-05-28
EGAS00001000525 Analysis_of_somatic_mutations_in_normal_blood__AML_and_MDS_samples Other
2013-05-31
EGAS00001000526 Integrative sequencing reveals alterations in untreated and castration resistant prostate cancer Other
2013-06-03
EGAS00001000528 Tagmentation-based Whole Genome Bisulfite Sequencing Other
2013-06-05
EGAS00001000530 Whole_exome_sequencing_of_inflammatory_bowel_disease_cases Other
2013-06-10
EGAS00001000531 Exome_sequence_of_probands_in_Barrett_s_oesophagus_families Other
2013-06-10
EGAS00001000532 Chromosome Y Philogeny in Sardinia Other
2013-06-10
EGAS00001000533 Chondromyxoid_fibroma Cancer Genomics
2013-06-11
EGAS00001000534 Analysis of DNA methylation in normal B cells and chronic lymphocytic leukemia Other
2013-06-12
EGAS00001000536 Identification of point mutations, expression perturbations, and gene fusions in T-cell acute lymphoblastic leukemia by RNA-seq Other
2013-06-14
EGAS00001000544 Consanguineous_families_with_CHD_KAIMRC Other
2013-06-17
EGAS00001000545 APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UG2G component) Other
2013-06-20
EGAS00001000546 Landscape of gene mutations in Down syndrome-related myeloid disorders Other
2013-06-25
EGAS00001000547 Distinct evolutionary trajectories of primary high grade serous ovarian cancers revealed through spatial mutational profiling Other
2013-06-25
EGAS00001000549 CPC-GENE Prostate Cancer Heterogeneity Study Other
2013-06-26
EGAS00001000551 Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma Other
2013-07-02
EGAS00001000552 Reference epigenomes generated as part of the International Human Epigenomics Consortium (IHEC) Other
2013-07-03
EGAS00001000554 Recurrent Somatic Mutations of PTPN1 in Primary Mediastinal B cell lymphoma and Hodgkin Lymphoma Other
2013-07-06
EGAS00001000557 Whole exome sequencing of peripheral T-cell lymphoma (PTCL) Other
2013-07-10
EGAS00001000558 DNA from colon cancer samples and matched normal samples was hybridized on Human 660W-Quad SNP arrays and sequenced in Illumina HiScanSQ. Other
2013-07-11
EGAS00001000559 ICGC Oesophageal adenocarcinoma - pilot samples Other
2013-07-19
EGAS00001000561 ICGC PedBrain DNA methylation sequencing Other
2013-07-24
EGAS00001000562 Whole_genome_sequencing_of_a_Grem1_mutant_human_tumour Whole Genome Sequencing
2013-07-25
EGAS00001000563 Comparison_of_transcriptional_response_of_induced_pluripotent_stem__iPS__cell_derived_and_monocyte_derived_macrophages_to_bacterial_lipopolysaccharide_stimulation Transcriptome Analysis
2013-07-25
EGAS00001000564 Lymphocyte_RNA_profiling Transcriptome Analysis
2013-07-26
EGAS00001000565 Hypermutation of the inactive X chromosome is a frequent event in cancer Other
2013-07-26
EGAS00001000566 Noninvasive detection of cancer-associated genome-wide hypomethylation and copy number aberrations by plasma DNA bisulfite sequencing Other
2013-07-28
EGAS00001000567 Autozygosity_pilot___British_Pakistani_from_Birmingham_2 Other
2013-07-30
EGAS00001000568 Tumor suppressor miR-133a modulates the prostate cancer epigenome by repressing BAZ2A Other
2013-07-31
EGAS00001000569 TMD_AMKL_targeted_follow_up Cancer Genomics
2013-07-31
EGAS00001000570 Targeted_sequencing_of_genes_recurrently_mutated_in_AML___part2 Cancer Genomics
2013-07-31
EGAS00001000571 POT1_splice_site_mutant_analysis Transcriptome Analysis
2013-08-01
EGAS00001000572 Whole genome sequencing of tumour and normal paired samples of diffuse intrinsic pontine gliomas Other
2013-08-01
EGAS00001000574 A sequence-based genetic dissection of human immune cell types and implications for immune-related disease. Other
2013-08-07
EGAS00001000575 Whole genome sequencing and whole exome sequencing of DIPG tumors and matched normal tissue Other
2013-08-08
EGAS00001000578 Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M-mutant pediatric high-grade gliomas Other
2013-09-11
EGAS00001000579 Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma Exome Sequencing
2013-09-13
EGAS00001000580 Whole genome sequencing of metastatic melanomas from a patient with primary resistance to BRAF inhibition Other
2013-09-17
EGAS00001000582 Resistance to anti-EGFR therapy in colorectal cancer Other
2013-09-20
EGAS00001000584 Assessing the impact of low frequency coding variants on disease risk using the Exomechip Other
2013-09-24
EGAS00001000585 Assessment of genomic copy number alterations in breast cancer Other
2013-09-25
EGAS00001000586 Determination_of_cell_specific_regulatory_enhancers_in_hematopoetic_models Gene Regulation Study
2013-09-25
EGAS00001000587 Epi_Tax_targeted_sequencing Cancer Genomics
2013-09-26
EGAS00001000588 Angiosarcoma_whole_exome Cancer Genomics
2013-09-26
EGAS00001000589 Angiosarcoma_targeted_pulldown_cancer_gene_panel Cancer Genomics
2013-09-26
EGAS00001000590 Angiosarcoma_RNA_sequencing Cancer Genomics
2013-09-26
EGAS00001000591 Sequencing_of_rare_human_histiocytic_tumour Cancer Genomics
2013-09-26
EGAS00001000592 HipSci-Whole Exome sequencing-healthy volunteers Other
2013-09-30
EGAS00001000593 HipSci-RNAseq-healthy volunteers Transcriptome Analysis
2013-10-02
EGAS00001000596 Breast_Cancer_Sequential_Sampling_Targeted_Capture Cancer Genomics
2013-10-11
EGAS00001000597 HKU Gastric Cancer Genomics study - WGS, DNA genotyping array, expression and methylation profiling Other
2013-10-12
EGAS00001000598 RB1 Gene Inactivation by Chromothripsis in Human Retinoblastoma Other
2013-10-14
EGAS00001000599 Genome-wide analysis of HPV integration in human cancers reveals recurrent, focal genomic instability Other
2013-10-14
EGAS00001000600 Measuring the level of relatedness between NGS datasets Other
2013-10-15
EGAS00001000602 Whole_exome_sequencing_for_HELIC Other
2013-10-16
EGAS00001000603 Use_of_Deep_Sequencing_to_Dectect_Clonal_Mutations_In_Sun_Exposed_Skin_Epidermis_PART2 Cancer Genomics
2013-10-16
EGAS00001000604 These are from Korean HCC samples with exome sequencing Other
2013-10-17
EGAS00001000605 Genome-wide SNP genotyping of Central African rainforest hunter-gatherers and neighbouring agriculturalists Other
2013-10-17
EGAS00001000606 Pseudogene_RNAseq Cancer Genomics
2013-10-17
EGAS00001000607 SHH medulloblastoma samples Other
2013-10-21
EGAS00001000610 RNA sequencing and Illumina 2.5M SNP array data collected from 675 commonly used human cancer cell lines. Other
2013-10-22
EGAS00001000612 PLCRC_study Cancer Genomics
2013-10-24
EGAS00001000613 Mosaic_Colorectal_Metastasis Cancer Genomics
2013-10-24
EGAS00001000615 Osteosarcoma_RNAseq Cancer Genomics
2013-10-24
EGAS00001000616 BIG_MS_Pilot Cancer Genomics
2013-10-24
EGAS00001000617 Identification_of_drug_resistance_genes_in_melanoma Other
2013-10-28
EGAS00001000619 Acquisition_of_additional_mutations_drives_accelerated_progression_of_NPM1_positive_CMML_to_AML_ Resequencing
2013-10-31
EGAS00001000620 Identification_of_rare_variants_associated_with_cardiovascular_traits_in_Cilento_isolates Other
2013-10-31
EGAS00001000621 Whole Genome Sequencing of Asian Lung Cancers: Second Hand Smoke is Not Responsible for Higher Incidence of Lung Cancer Among Asian Never-Smokers Other
2013-11-01
EGAS00001000622 Pharmacological and genomic profiling identifies NFκB-targeted treatment strategies for mantle cell lymphoma Other
2013-11-05
EGAS00001000624 WTCCC2 project Glaucoma (GL) samples Other
2013-11-06
EGAS00001000625 Divergence between high metastatic tumor burden and low circulating tumor DNA concentration in metastasized breast cancer Other
2013-11-12
EGAS00001000626 Haemoglobin_E_beta_thalassaemia_in_a_patient_group_from_Sri_Lanka Other
2013-11-12
EGAS00001000627 Leiden_melanomafamilies Whole Genome Sequencing
2013-11-13
EGAS00001000628 WTCCC2 BO (Barretts oesophagus) samples Other
2013-11-15
EGAS00001000630 Illumina ExomeChip genotyping data from the Cretan Greek isolate collection HELIC MANOLIS Other
2013-11-22
EGAS00001000641 Mutational context and diverse clonal development in early and late bladder cancer Other
2013-11-26
EGAS00001000642 Quantification of chromosomal copy number aberrations by shallow whole-genome sequencing Other
2013-11-27
EGAS00001000643 Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas Other
2013-11-27
EGAS00001000644 Genome of the Netherlands Other
2013-11-28
EGAS00001000646 The study provides comprehensive access to the set of EGA studies which may be useful as controls. Other
2013-12-06
EGAS00001000647 A Genomics-Based Classification of Human Lung Tumors Other
2013-12-10
EGAS00001000648 FinHer_Breast_Cancer_Study Cancer Genomics
2013-12-11
EGAS00001000649 GEL_WGS_Comparison Cancer Genomics
2013-12-11
EGAS00001000650 Frequent mutations in chromatin-remodelling genes in pulmonary carcinoids Other
2013-12-12
EGAS00001000651 Mutational_Signatures_of_relapse_in_rectal_cancer_FFPE_samples_in_the_CR07_clinical_trial Cancer Genomics
2013-12-13
EGAS00001000652 Microsatellite data show recent demographic expansions in sedentary but not in nomadic human populations in Africa and Eurasia. Other
2013-12-13
EGAS00001000653 CD74-NRG1 fusions in lung adenocarcinoma Other
2013-12-17
EGAS00001000654 PCGP Ph-like ALL Other
2013-12-17
EGAS00001000655 Combination_therapies_for_personalized_cancer_medicine Cancer Genomics
2013-12-17
EGAS00001000658 Illumina Human Exome (ExomeChip) genotype data from the Pomak villages in Greece (HELIC Pomak Isolate). 1040 samples all >=16 years old. Other
2013-12-19
EGAS00001000659 Identification of novel fusion genes in lung cancer using breakpoint assembly of transcriptome sequencing data Other
2013-12-23
EGAS00001000660 High number of somatic mutations found in the healthy blood compartment of a 115-year-old woman reveals oligoclonal hematopoiesis Other
2013-12-24
EGAS00001000661 Whole-exome analysis of corticotropin-independent Cushing's syndrome Other
2013-12-26
EGAS00001000662 Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma Other
2014-01-09
EGAS00001000663 MPN_mutation_order_followup Cancer Genomics
2014-01-09
EGAS00001000664 Whole-Genome Sequencing of 128 Ashkenazi Jewish individuals Other
2014-01-09
EGAS00001000665 Integrated genomic characterization of adrenocortical carcinoma Other
2014-01-13
EGAS00001000667 Genomic architecture and evolution of clear cell renal cell carcinomas defined by multiregion sequencing Other
2014-01-14
EGAS00001000668 Study on the consequences of prenatal famine exposure on DNA methylation. Other
2014-01-15
EGAS00001000669 An oncogenic enhancer-rearrangement causes concomitant deregulation of EVI1 and GATA2 in leukemia. Targeted resequencing of chromosomal regions centered on 3q21 and 3q26 in conjunction with RNA-Seq from Acute Myeloid Leukemia patients. Other
2014-01-20
EGAS00001000671 Whole genome sequencing of Japanese HCCs Other
2014-01-21
EGAS00001000672 WTCCC2 People of the British Isles (POBI) genotypes Other
2014-01-21
EGAS00001000673 Exploration of CNV’s and SNV’s in cancers with well-known genetic rearrangements: Identification of additional genetic changes in rearrangements-driven cancer Other
2014-01-21
EGAS00001000674 High-throughput Detection of Clinically Relevant Mutations in Archived Tumor Samples By Multiplexed PCR and Next Generation Sequencing Other
2014-01-21
EGAS00001000677 Whole exome sequencing of 103 pairs BLCA-CN Other
2014-01-22
EGAS00001000678 WGS of liver cancer in the Japanese population Other
2014-01-23
EGAS00001000679 Integrative genomic profiling of hepatocellular adenomas reveals recurrent FRK activating mutations and mutational processes of malignant transformation Other
2014-01-24
EGAS00001000680 Molecular Signature of Saudi Thyroid Cancer Using whole exome sequencing Other
2014-01-24
EGAS00001000682 Epigenetic Intratumor Heterogeneity and Clonal Evolution in Aggressive Prostate Cancer Other
2014-01-27
EGAS00001000685 Recurrent epimutations activate gene body promoters in primary glioblastoma Other
2014-01-28
EGAS00001000687 Illumina Human OmniExpress genotyping data from the Cretan Greek isolate collection HELIC MANOLIS Other
2014-01-29
EGAS00001000689 BLUEPRINT EpiVar Whole Genome Sequencing Other
2014-01-30
EGAS00001000691 miRNA_expression_in_response_to_LPS_stimulus_in_macrophages Transcriptome Analysis
2014-02-05
EGAS00001000692 FFPE_CPA_Accreditation_Study__Part_2 Cancer Genomics
2014-02-05
EGAS00001000698 Neuromics / RD-Connect - Huntington's disease Other
2014-02-06
EGAS00001000703 MDS_Sequential_Treatment_Validation Cancer Genomics
2014-02-07
EGAS00001000704 Metastatic_breast_cancer_targeted_gene_screen Cancer Genomics
2014-02-07
EGAS00001000706 Whole-Genome sequencing of hepatocellular carcinomas Other
2014-02-18
EGAS00001000707 BASIS_RNAseq Cancer Genomics
2014-02-18
EGAS00001000708 Integrative genomic profiling of large-cell neuroendocrine carcinomas reveals distinct subtypes of high-grade neuroendocrine lung tumors Other
2014-02-19
EGAS00001000709 whole-genome sequencing in 17 ESCC cases and whole-exome sequencing in 71 cases Other
2014-02-20
EGAS00001000711 Identification_of_cardiovascular_biomarkers_through_an_integrative_omics_approach Transcriptome Analysis
2014-02-25
EGAS00001000712 Whole exome sequencing of 49 tumor-blood pairs and transcriptome sequencing of 44 tumors for adrenocortical tumors Other
2014-02-26
EGAS00001000713 UK10K COHORT IMPUTATION Other
2014-02-26
EGAS00001000714 Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4 Other
2014-02-28
EGAS00001000716 Myelodysplastic cells in patients re-program mesenchymal stromal cells to establish a transplantable stem cell-niche disease unit. Other
2014-02-28
EGAS00001000717 Autozygosity_pilot___QMUL Other
2014-03-05
EGAS00001000718 Human_Evolution_3B Whole Genome Sequencing
2014-03-05
EGAS00001000719 Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouse Other
2014-03-06
EGAS00001000720 Location specific ACVR1, FGFR1 and TP53 mutations in pediatric glioblastomas in conjunction with H3.3 K27M. Other
2014-03-06
EGAS00001000721 Germline and somatic SMARCA4 mutations characterize small-cell carcinoma of the ovary, hypercalcemic type. Other
2014-03-06
EGAS00001000722 UQCCR/QCMG brain metastasis sequence analysis Other
2014-03-07
EGAS00001000723 ICGC Oesophageal adenocarcinoma - normal samples Other
2014-03-07
EGAS00001000724 ICGC Oesophageal adenocarcinoma - 100 tumour samples Other
2014-03-07
EGAS00001000725 ICGC Oesophageal adenocarcinoma - tumour samples Other
2014-03-07
EGAS00001000726 ICGC Oesophageal adenocarcinoma - Barrett's samples Other
2014-03-07
EGAS00001000727 ICGC Oesophageal adenocarcinoma - lymph-node samples Other
2014-03-07
EGAS00001000728 SPECTA__NGS_Screening_Program_for_Efficient_Clinical_Trial_Access Cancer Genomics
2014-03-07
EGAS00001000729 Whole Exome Sequencing of cohorts of Mutant Braf mouse model melanoma DNA and germline DNA. Other
2014-03-10
EGAS00001000730 Metastatic_Prostate_Follow_Up Cancer Genomics
2014-03-14
EGAS00001000731 Plasma RNA sequencing Other
2014-03-14
EGAS00001000732 TMD_AMKL_targeted_follow_up_part_2 Cancer Genomics
2014-03-14
EGAS00001000733 Barcelona_kids_with_melanoma Whole Genome Sequencing
2014-03-17
EGAS00001000734 Genome wide association study on coronary heart disease in patients with familial hypercholesterolemia Other
2014-03-18
EGAS00001000736 Exome-seq, RNA-Seq, SNP array profiling of gastric tumor samples and cell lines. Other
2014-03-18
EGAS00001000737 Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue Other
2014-03-19
EGAS00001000738 Whole-genome sequencing of bladder cancers of various stages and grades to search for driver mutations, chromosome-scale somatic changes, mutation signatures and clonal structures. Other
2014-03-20
EGAS00001000740 DNA_repair_in_BLM_deficient_hiPSCs Other
2014-03-20
EGAS00001000741 Assessment_of_epigenetic_variation_in_human_iPS_cells_Medip Epigenetics
2014-03-20
EGAS00001000742 Role_of_Epigenetic_Memory_in_Human_Induced_Pluripotent_Stem_Cells_Pilot Transcriptome Analysis
2014-03-20
EGAS00001000743 Myeloma_Follow_up_Pilot Cancer Genomics
2014-03-20
EGAS00001000744 ICGC medulloblastoma whole genome sequencing data, ICGC release 16 Other
2014-03-21
EGAS00001000747 ESGI_Exome_sequencing_in_Circulating_Tumor_Cells_to_determine_therapy_related_markers_____ Other
2014-03-26
EGAS00001000749 Study of pediatric hepatocellular carcinoma caused by bile salt export pump deficiency Other
2014-03-27
EGAS00001000750 Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis. Other
2014-03-28
EGAS00001000751 Transposome_Bisulfite_Sequencing Cancer Genomics
2014-03-28
EGAS00001000752 BLUEPRINT EpiVar RNA-seq for Naive naive CD4+ T-cells Other
2014-03-28
EGAS00001000753 BLUEPRINT EpiVar ChIP-seq for naive CD4+ T-cells Other
2014-03-28
EGAS00001000756 Metastatic_Prostate_Follow_Up_2 Cancer Genomics
2014-03-31
EGAS00001000758 TCELL_PILOT_ATAC_SEQ Transcriptome Analysis
2014-04-02
EGAS00001000760 Unraveling metastatic progression of breast cancer Other
2014-04-03
EGAS00001000761 RNAseq data to study PRPF6 regulated splice forms in colon cancer cell lines Other
2014-04-03
EGAS00001000762 Genetics_and_Networks_of_Congenital_Heart_Defects Other
2014-04-07
EGAS00001000763 Expressed_fusion_transcripts_in_rare_bone_tumours Cancer Genomics
2014-04-08
EGAS00001000764 SINGLE_CELL_ANALYSIS_OF_IN_VITRO_ERYTHROPOIESIS Transcriptome Analysis
2014-04-10
EGAS00001000765 MPN_TGS2_Follow_up___PT1_Vori_other Cancer Genomics
2014-04-10
EGAS00001000767 Next generation sequencing of sporadic schwannomatosis samples Other
2014-04-11
EGAS00001000768 Low_Coverage_Sequencing_of_rare_human_histiocytic_tumour Cancer Genomics
2014-04-14
EGAS00001000769 Whole genome sequencing of 50 trios, where the child is affected with ID, and the parents are unaffected Other
2014-04-15
EGAS00001000772 MYD88/TLR mutations in CLL Other
2014-04-22
EGAS00001000773 WTCCC2 Visceral Leishmaniasis (VL) samples Other
2014-04-24
EGAS00001000775 Deciphering Developmental Disorders (DDD) Other
2014-04-28
EGAS00001000789 Moles Cancer Genomics
2014-04-30
EGAS00001000790 Exploration_of__mutational_processes_in_human_cancer_cell_lines__Exome Cancer Genomics
2014-04-30
EGAS00001000793 Two lung cancer cell lines with EGFR mutations, PC-9 and KHM-3S, were either treated with Tarceva for 24 hours or left untreated. The gene expression profiles were examined by RNAseq, and the genome wide binding profiles of total STAT3 and pSTAT3 were characterized by ChIPseq. Other
2014-04-30
EGAS00001000800 Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_ Whole Genome Sequencing
2014-05-06
EGAS00001000801 TBA Whole Genome Sequencing
2014-05-06
EGAS00001000802 TBA Whole Genome Sequencing
2014-05-06
EGAS00001000803 TBA Whole Genome Sequencing
2014-05-06
EGAS00001000805 RNA-seq data from the EUROBATS Project in four tissues: Fat, LCL, Skin and whole Blood. Other
2014-05-06
EGAS00001000807 Imputation-Based Meta-Analysis of Severe Malaria in Three African Populations Other
2014-05-08
EGAS00001000808 Whole_exome_sequencing_CHD_trios Other
2014-05-08
EGAS00001000809 TRACERx: TRAcking non-small cell lung Cancer Evolution through therapy (Rx). Pilot Study. Multi-region sequencing of early-stage NSCLCs. Other
2014-05-08
EGAS00001000812 Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma Cancer Genomics
2014-05-09
EGAS00001000813 RNAseq___Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma Cancer Genomics
2014-05-09
EGAS00001000814 Study_to_investigate_the_prevalence__of_leukaemic_mutations_in_whole_blood_DNA_in_a_cohort_of_blood_donors Resequencing
2014-05-09
EGAS00001000815 Identification_of_drug_resistance_genes_in_melanoma_by_mRNA_gene_expression Transcriptome Analysis
2014-05-13
EGAS00001000816 Identification_of_drug_resistance_genes_in_melanoma_by_small_RNAs_expression_analysis Transcriptome Analysis
2014-05-13
EGAS00001000817 A WTCCC2 genome-wide association study for psychosis endophenotype (PE) in individuals from UK, Germany, Holland, Spain and Australia. Other
2014-05-13
EGAS00001000824 Diverse modes of genomic alterations in hepatocellular carcinoma Other
2014-05-15
EGAS00001000825 Whole_Exome_Sequencing_of_INTERVAL Other
2014-05-19
EGAS00001000826 Reproducibility of variant calls in replicate next generation sequencing experiments Other
2014-05-19
EGAS00001000828 CGP_CORE_CELL_LINES___RNA_seq Cancer Genomics
2014-05-22
EGAS00001000830 Mesothelioma_Whole_Genomes Cancer Genomics
2014-05-22
EGAS00001000836 FFPE_Normal_Panel_V3_Cancer_Panel Cancer Genomics
2014-05-30
EGAS00001000837 Lung_Progression_versus_Regression_Whole_Genome_Sequencing Cancer Genomics
2014-05-30
EGAS00001000839 Targeting the DNA Repair Pathway in Ewing Sarcoma Other
2014-06-02
EGAS00001000840 Spatial and temporal diversity in genomic instability processes define early stage lung cancer evolution. Other
2014-06-03
EGAS00001000841 HumanMethylation450K data from Purified Plasma Cells of Monoclonal gammopathy of unknown significance and Multiple myeloma patients and Healthy donors Other
2014-06-03
EGAS00001000845 Genomic analysis of Smoothened inhibitor resistance in basal cell carcinoma Other
2014-06-03
EGAS00001000849 Celiac disease case-control North Indian Immunochip dataset Other
2014-06-04
EGAS00001000850 Detection of Clinically Relevant Genetic Variantsin Autism Spectrum Disorderby Whole-Genome Sequencing Whole Genome Sequencing
2014-06-04
EGAS00001000851 Primary_angiosarcoma_Whole_Genome_Sequencing Cancer Genomics
2014-06-05
EGAS00001000852 Benchmark and validation of whole exome sequencing of a trio and singleton Other
2014-06-05
EGAS00001000853 Whole exome sequencing for gallbladder cancer in Xinhua Hospital Affiliated to Shanghai Jiao Tong University, School of Medicine Other
2014-06-06
EGAS00001000854 Systems biology of Colorectal Cancer Other
2014-06-10
EGAS00001000855 Genomic landscape of Ewing sarcoma (ICGC project) Other
2014-06-10
EGAS00001000857 Deep_sequencing_of_melanoma_for_driver_mutations Cancer Genomics
2014-06-12
EGAS00001000858 Integrative_genome_profiling_in_AML Cancer Genomics
2014-06-12
EGAS00001000859 Anaplastic_Meningioma_WGS_X10 Cancer Genomics
2014-06-12
EGAS00001000860 Use_of_deep_sequencing_to_detect_clonal_mutations_in_sun_exposed_human_epidermis___whole_genome Cancer Genomics
2014-06-12
EGAS00001000864 The_life_history_of_colorectal_cancer_metastases_study_WGS_X10 Cancer Genomics
2014-06-18
EGAS00001000865 HipSci_Illumina 450K Methylation analysis_Healthy volunteers Other
2014-06-18
EGAS00001000866 HipSci HumanExome BeadChip analysis-Healthy volunteers Other
2014-06-18
EGAS00001000867 HipSci HumanHT_12v4 Expression BeadChip analysis-Healthy volunteers Other
2014-06-18
EGAS00001000869 Colorectal_organoids_and_tumoroids___pulldown Cancer Genomics
2014-06-25
EGAS00001000870 BLUEPRINT EpiVar ChIP-seq of Monocytes & Neutrophils Other
2014-06-25
EGAS00001000872 Chugai_colorectal_organoid_sequencing Cancer Genomics
2014-06-26
EGAS00001000874 Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_ Cancer Genomics
2014-07-01
EGAS00001000875 Loss of functional mutation in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan Anemia Other
2014-07-02
EGAS00001000876 Characterization_of_iPSC_derived_macrophages___cardiovascular_pilot Transcriptome Analysis
2014-07-02
EGAS00001000877 Whole genome DNA sequencing for two long-lived humans. Other
2014-07-02
EGAS00001000878 Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity Other
2014-07-03
EGAS00001000879 Prognostic_factors_in_prostate_cancer__deep_sequencing_pilot_project_TAPG Cancer Genomics
2014-07-03
EGAS00001000880 Myeloma_Targeted_Follow_up_Study Cancer Genomics
2014-07-03
EGAS00001000881 Colorectal_organoids_and_tumour_tissue Cancer Genomics
2014-07-03
EGAS00001000882 Succession Of Transiently Active Tumour-Initiating Cell Clones inHuman Pancreatic Cancer Other
2014-07-07
EGAS00001000883 Study on the proliferation history of colorectal adenomas Other
2014-07-07
EGAS00001000884 Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma Other
2014-07-08
EGAS00001000885 Whole Genome Sequencing to track subclonal heterogeneity in 18 samples from 3 Chronic Lymphocytic Leukemia patients subjected to repeated cycles of therapy. Other
2014-07-08
EGAS00001000886 WTCCC2 Reading and Mathematics (RM) samples Other
2014-07-10
EGAS00001000888 65 prostate cancer cases WGS and transcriptome sequencing project Other
2014-07-16
EGAS00001000889 TEST_STUDY for submitter testing Other
2014-07-21
EGAS00001000890 Multisite_Breast_Cancer_Whole_Genome Cancer Genomics
2014-07-21
EGAS00001000891 Multisite_Primary_Breast_Cancer Cancer Genomics
2014-07-21
EGAS00001000892 Chordoma_Extension_Study Cancer Genomics
2014-07-23
EGAS00001000895 Chordoma_Extension__known_cancer_genes_ Cancer Genomics
2014-07-23
EGAS00001000896 An isolated cohort of samples from the Greek island of Crete that have been genotyped on the Illumina CoreExome array. Other
2014-07-23
EGAS00001000899 SeqControl: Process Control for DNA Sequencing Other
2014-07-23
EGAS00001000900 Canadian Prostate Cancer Genome Network Other
2014-07-23
EGAS00001000901 The Genomic Landscape of Childhood and Adolescent Melanoma Other
2014-07-23
EGAS00001000902 Metastatic_Breast_Cancer_Whole_Genome Cancer Genomics
2014-07-23
EGAS00001000904 Exome sequencing to identify predisposition to Wilms tumour Other
2014-07-24
EGAS00001000906 Mutations in the SIX1/2 pathway and the DROSHA/DGCR8 miRNA microprocessor complex underlie high-risk blastemal type Wilms tumors Other
2014-07-28
EGAS00001000907 Von Hippel-Lindau syndrome multi-region exome sequencing project from two patients undertaken at Cancer Research UK's London Research Institute Other
2014-07-29
EGAS00001000908 Evolution of the African pygmy phenotype Other
2014-07-29
EGAS00001000909 Normal brain controls for ICGC PedBrain DNA methylation sequencing Other
2014-07-30
EGAS00001000910 DNA methylation repeatability in the Lothian Birth Cohorts of 1921 and 1936. Other
2014-07-30
EGAS00001000913 WTCCC3_Anorexia_Nervosa Population Genomics
2014-07-31
EGAS00001000916 Developmental_Dysplasia_of_the_Hip__DDH_ Population Genomics
2014-07-31
EGAS00001000917 ARGO_GWAS Population Genomics
2014-07-31
EGAS00001000918 Genome_wide_association_study_of_vaccine_responses_in_infants_living_in_the_Developing_World__VaccGene___Phase_II_African_Cohorts Population Genomics
2014-07-31
EGAS00001000924 Genotyping_of_additional_Inflammatory_Bowel_Disease_cases___2014 Other
2014-07-31
EGAS00001000925 Comprehensive genomic profiles of small cell lung cancer Other
2014-07-31
EGAS00001000926 Study of non-clear cell renal cell carcinoma Other
2014-08-01
EGAS00001000927 A Comparative Analysis of Algorithms for Somatic SNV Detection in Cancer Other
2014-08-04
EGAS00001000930 Intra-tumor heterogeneity of localized lung adenocarcinomas defined by multi-region sequencing Other
2014-08-05
EGAS00001000932 Genetic Landscape of Esophageal Squamous Cell Carcinoma Defined by Exome Sequencing on Chinese Patient Cohort and Cell Lines Other
2014-08-06
EGAS00001000933 Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas Other
2014-08-07
EGAS00001000934 PREDICT___Whole_Genomes Cancer Genomics
2014-08-07
EGAS00001000935 Single_Cell_Sequencing_of_Sperm__scSperm_ Population Genomics
2014-08-08
EGAS00001000936 Ischemic stroke in a Swedish case-control study. Other
2014-08-10
EGAS00001000938 Whole Exome Sequencing of healthy Spanish individuals Other
2014-08-11
EGAS00001000940 Whole genome study of Hurthle cell thyroid carcinoma Other
2014-08-12
EGAS00001000941 Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes Other
2014-08-14
EGAS00001000942 Tracking the origins and drivers of subclonal metastatic expansion in prostate cancer Other
2014-08-15
EGAS00001000943 Genomic analysis of seminomas Other
2014-08-18
EGAS00001000946 Mechanisms_of_patient_response_to_Dabrafenib_in_Melanoma Cancer Genomics
2014-08-22
EGAS00001000947 ATAC_SEQ_MAIN___PHASE_1 Transcriptome Analysis
2014-08-23
EGAS00001000948 DKFZ-HIPO Project H021/NCT MASTER Other
2014-08-26
EGAS00001000949 Clinical and Molecular Investigation of Familial CEBPA-mutated Acute Myeloid Leukaemia Other
2014-08-28
EGAS00001000950 Whole exome and transcriptome sequencing of biliary tract cancer Other
2014-08-29
EGAS00001000951 BLUEPRINT ChIP-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity Other
2014-08-29
EGAS00001000952 Dynamics of genomic clones in breast cancer patient xenografts at single cell resolution Other
2014-08-29
EGAS00001000953 BLUEPRINT RNA-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity Other
2014-09-01
EGAS00001000954 BLUEPRINT DNase accessibility of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity Other
2014-09-01
EGAS00001000955 EBV_AID_project Cancer Genomics
2014-09-03
EGAS00001000957 Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X Other
2014-09-04
EGAS00001000958 TGS___Comprehensive_Molecular_Characterization_of_Colorectal_Cancer_Metastases__MOSAIC_ Cancer Genomics
2014-09-05
EGAS00001000959 APCDR AGV Project: The African Genome Variation Project(dense array genotyping data) Other
2014-09-05
EGAS00001000960 APCDR AGV Project: Whole genome sequencing of 3 African populations (curated data) Other
2014-09-05
EGAS00001000961 Cross-species genomics identifies TAF12, NFYC and RAD54L as novel choroid plexus carcinoma oncogenes Other
2014-09-05
EGAS00001000962 Plasma DNA aberrations in systemic lupus erythematosus revealed by genomic and methylomic sequencing Other
2014-09-06
EGAS00001000963 The Druze analysis group Other
2014-09-08
EGAS00001000968 Origins and functional consequence of somatic mitochondrial DNA mutations Other
2014-09-10
EGAS00001000969 HipSci___Whole_Exome_sequencing___Bardet_Biedl_Syndrome Other
2014-09-10
EGAS00001000971 Exome sequencing of 1000 population control samples from the UK 1958 birth cohort Other
2014-09-15
EGAS00001000973 High coverage target resequencing of coding and regulatory regions of 38 Parkinson disease genes associated either to the Mendelian or the sporadic forms of the disease Other
2014-09-16
EGAS00001000974 Genetic landscape of malignant peripheral nerve sheath tumors Other
2014-09-17
EGAS00001000975 Signatures of Aristolochic Acid Mutagenesis in Bladder Cancer Other
2014-09-18
EGAS00001000978 Cancer_Cell_Line_Exome_Sequencing_ Cancer Genomics
2014-09-19
EGAS00001000979 Pulldown_DNA_methylation_study_v2 Cancer Genomics
2014-09-19
EGAS00001000980 Confirmation of a founder effect in a Northern European population (FRL) of a new beta-globin variant: HBB:c.23_26dup (codons 8/9 (+AGAA)) Other
2014-09-22
EGAS00001000981 We evaluate the PGD/PGS including 129 couples with NGS test and 266 couples with SNP-array test for the detection of embryonic chromosomal abnormalities. Other
2014-09-23
EGAS00001000982 Frequent alterations in cytoskeleton remodeling genes in primary and metastatic Chinese lung adenocarcinomas Other
2014-09-24
EGAS00001000983 SOFT_study___sequencing_premenopausal_breast_cancer Cancer Genomics
2014-09-24
EGAS00001000985 _RNAseq___Colorectal_organoids_and_tumoroids Cancer Genomics
2014-09-24
EGAS00001000988 30X_WGS_sequencing_of_100_individuals_from_the_general_Greek_population Other
2014-09-26
EGAS00001000990 Fetal hemoglobin in sickle cell disease patients from Tanzania Other
2014-09-26
EGAS00001000991 Therapeutic Resistance to PI3K-alpha Inhibitors Other
2014-09-26
EGAS00001000992 Human melanoma samples with and without resistance to BRAF inhibitor therapy Other
2014-09-26
EGAS00001000993 Identification of causal mutation in two patients with Sotos Syndrome Features Other
2014-09-29
EGAS00001000995 McGill Epigenomics Mapping Centre Other
2014-10-01
EGAS00001000996 Illumina HumanOmniExpress genotyping data from the TEENAGE (TEENs of Attica: Genes and Environment) study. Other
2014-10-03
EGAS00001001000 An RCOR1 loss-associated gene expression signature identifies a prognostically significant DLBCL subgroup Other
2014-10-08
EGAS00001001001 Illumina HumanCoreExome genotyping data from the TEENAGE (TEENs of Attica: Genes and Environment) study. Other
2014-10-09
EGAS00001001002 Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets Other
2014-10-09
EGAS00001001003 An efficient and comprehensive strategy for genetic diagnostics of polycystic kidney disease Other
2014-10-09
EGAS00001001004 First genome-wide association study in an Australian Aboriginal population provides insights into genetic risk factors for Body Mass Index and Type 2 Diabetes Other
2014-10-10
EGAS00001001009 Biased allelic expression in human primary fibroblast single cells. Other
2014-10-14
EGAS00001001011 MDS Sequencing Project_Cancer Cell Other
2014-10-17
EGAS00001001012 The NIHR BioResource Rare Diseases BRIDGE consortium sequencing projects Other
2014-10-20
EGAS00001001013 Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness Other
2014-10-20
EGAS00001001014 Spatial heterogeneity in medulloblastoma Other
2014-10-21
EGAS00001001015 Exomes of High-risk Prostate cancer Other
2014-10-23
EGAS00001001016 A Cancer Cell-Line Titration Series for Evaluating Somatic Classification Exome Sequencing
2014-10-23
EGAS00001001017 Genotype data of osteoarthritis cases from the UK collected by the arcOGEN Consortium (http://www.arcogen.org.uk/). Other
2014-10-27
EGAS00001001018 Whole-genome plasma sequencing reveals focal amplifications as a driving force in metastatic prostate cancer Other
2014-10-29
EGAS00001001019 (h)MeDIP-Seq of high-risk prostate cancer Other
2014-10-29
EGAS00001001020 Genome-wide prediction of human embryos Other
2014-10-30
EGAS00001001021 Exome_sequencing_of_EBV_driven_lymphoma Cancer Genomics
2014-10-30
EGAS00001001023 Whole genome sequencing of ASD quartet families Other
2014-10-31
EGAS00001001024 Lengthening and shortening of plasma DNA in hepatocellular carcinoma patients Other
2014-10-31
EGAS00001001025 Comprehensive miRNA Sequence Analysis Reveals Survival Differences in Diffuse Large B-cell Lymphoma Patients Other
2014-10-31
EGAS00001001026 Prediction and quantification of splice events from RNA-seq data Other
2014-10-31
EGAS00001001028 Genomic Alterations in Gingivo-buccal Cancer: ICGC-India Project_YR02 Other
2014-11-03
EGAS00001001033 Spatial and temporal genomic evolution in glioblastoma Other
2014-11-09
EGAS00001001035 Identification_of_drug_resistance_genes_in_cancer_cell_lines_by_insertional_mutagenesis Cancer Genomics
2014-11-12
EGAS00001001036 English Longitudinal Study of Ageing Genome-wide genotyping using the Illumina HumanOmni2.5-8 Other
2014-11-13
EGAS00001001041 Spatio-temporal evolution of the primary glioblastoma genome Other
2014-11-17
EGAS00001001044 To reveal the spectrum of gene mutations in grade II/III gliomas, whole exome sequencing of 52 samples including 4 multi-regional and 10 multi-time points sampling cases and 291 SNP-array were performed. Other
2014-11-19
EGAS00001001045 To reveal the spectrum of gene mutations in grade II/III gliomas, whole exome sequencing of 52 samples including 4 multi-regional and 10 multi-time points sampling cases and 293 SNP-array were performed. Other
2014-11-19
EGAS00001001047 Finnish_population_cohort_genotyping_B Population Genomics
2014-11-19
EGAS00001001048 Preeclampsia InterPregGen Consortium: GWAS meta-analysis summary statistics for European fetal preeclampsia cases versus controls and GWAS genotype data for European fetal preeclampsia cases Other
2014-11-19
EGAS00001001051 Methylation differences in trisomy 21 using monozygotic twins Other
2014-11-26
EGAS00001001052 Skin Adenocarcinoma Genome Sequencing Other
2014-12-01
EGAS00001001054 GIST_SSGXVIII_trial_targeted_gene_sequencing Cancer Genomics
2014-12-02
EGAS00001001056 WGS and WES of 78 pairs Chinese gastric cancer Other
2014-12-04
EGAS00001001059 Cell_lines_with_telomere_fusion_induced_rearrangements Cancer Genomics
2014-12-04
EGAS00001001060 CRISPR_screen_M14__NCI_H3122 Cancer Genomics
2014-12-04
EGAS00001001066 Genome-wide SNP genotyping and DNA methylation epigenotyping of African rainforest hunter-gatherers and neighbouring agriculturalists Other
2014-12-05
EGAS00001001067 Integrated genomic, transcriptional and epigenomic analyses in germinal center-cell lymphomas link the mutation landscape with differential DNA methylation in Burkitt lymphoma Other
2014-12-08
EGAS00001001077 The mission of the BIOS Consortium is to create a large-scale data infrastructure and to bring together BBMRI researchers focusing on integrative omics studies in Dutch Biobanks. Other
2014-12-09
EGAS00001001082 2014 chunnam AML analysis Other
2014-12-10
EGAS00001001084 Whole exome sequencing reveals the mutational spectrum of testicular germ cell tumours Other
2014-12-10
EGAS00001001085 Capture Hi-C identifies the chromatin interactome of colorectal cancer risk loci Other
2014-12-10
EGAS00001001086 Exome_sequencing_of_short_SGA_children_with_IGF_I_and_insulin_resistance Other
2014-12-10
EGAS00001001090 GWAS of tuberculosis in Russia Other
2014-12-15
EGAS00001001093 Exome Sequencing Of 75 Individuals From Multiply Affected Coeliac Families Other
2014-12-16
EGAS00001001095 NGS_based_viability_screening_using_haploid_cell_line Cancer Genomics
2014-12-16
EGAS00001001099 ABIS_1_MeDIP-seq Other
2014-12-17
EGAS00001001102 RB Loss in Resistant EGFR Mutant Lung Adenocarcinomas that Transform to Small Cell Lung Cancer Other
2014-12-19
EGAS00001001103 Whole-exome sequencing of Fanconi anemia Other
2014-12-28
EGAS00001001108 Exome Sequencing Reveals Frequent Inactivating Mutations in BAP1, ARID1A, and PBRM1 in Intrahepatic Cholangiocarcinomas Other
2015-01-08
EGAS00001001110 Blueprint RNAseq profile of purified plasma cells from multiple myeloma patients and tonsils of healthy donors Other
2015-01-09
EGAS00001001112 Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers Other
2015-01-12
EGAS00001001113 Whole-exome and targeted sequencing of pediatric hyperdiploid B-cell precursor acute lymphoblastic leukemia Other
2015-01-13
EGAS00001001114 Whole_exome_sequencing_of_additional_thyroid_disease_cases Other
2015-01-13
EGAS00001001115 Genetic_profiling_of_mucosal_melanoma Other
2015-01-14
EGAS00001001116 ESGI___Whole_Genome_Sequencing_of_samples_from_the_Cilentogen_isolates Population Genomics
2015-01-14
EGAS00001001117 ESGI___Whole_Genome_Sequencing_of_NSPHS_samples Population Genomics
2015-01-14
EGAS00001001119 ESGI___Whole_Genome_Sequencing_of_samples_from_the_Croatian_isolated_populations_ Population Genomics
2015-01-14
EGAS00001001123 ESGI___Whole_Genome_Sequencing_of_samples_from_the_INGI_Val_Borbera_genetic_isolate__X10_ Population Genomics
2015-01-14
EGAS00001001124 Congenital_anosmia_1 Other
2015-01-14
EGAS00001001125 ESGI___Whole_Genome_Sequencing_of_samples_from_the_ORCADES_cohort__X10__ Cancer Genomics
2015-01-14
EGAS00001001127 MiR expression profiles of paired primary colorectal cancerand metastases by next-generation sequencing Other
2015-01-19
EGAS00001001129 IBDCA_Edinburgh Other
2015-01-20
EGAS00001001130 Genome-wide association study of response to warfarin in a UK prospective cohort Other
2015-01-21
EGAS00001001132 DPY30_ChIP_seq Epigenetics
2015-01-22
EGAS00001001133 mFAST-SeqS Other
2015-01-22
EGAS00001001134 Genome-wide association analysis on five isolated populations - Erasmus Rucphen Family (ERF) Study Other
2015-01-22
EGAS00001001135 Intratumor heterogeneity evaluation in primary HCC cells Other
2015-01-23
EGAS00001001137 HipSci___RNAseq___Rare_Monogenic Diabetese Other
2015-01-26
EGAS00001001139 Whole genome and RNA sequencing of paediatric glioblastoma in the ICGC PedBrain project Other
2015-01-26
EGAS00001001140 HipSci___Whole_Exome_sequencing___Monogenic_Diabetes Other
2015-01-26
EGAS00001001145 FWO_project_G_0687_12_X10_WGS Cancer Genomics
2015-01-29
EGAS00001001146 Efficacy of JAK/STAT pathway inhibition in murine xenograft models of early T-cell precursor (ETP) acute lymphoblastic leukemia Other
2015-01-30
EGAS00001001147 463 newly diagnosed patients with Multiple Myeloma underwent whole exome sequencing of tumour and peripheral blood DNA. Other
2015-02-02
EGAS00001001149 Mapping_regulatory_variation_in_sensory_neurons_using_IPS_lines_from_the_HIPSCI_project Gene Regulation Study
2015-02-05
EGAS00001001150 A personalised medicine approach for ponatinib-resistant chronic myeloid leukaemia Other
2015-02-05
EGAS00001001153 Aplastic anemia Other
2015-02-10
EGAS00001001155 Anaplastic_Meningioma_V3__cancer_gene_panel Cancer Genomics
2015-02-11
EGAS00001001158 Leeds_Melanoma_Cohort Cancer Genomics
2015-02-12
EGAS00001001159 The BC Cancer Agency's Personalized Onco-Genomics Project Cancer Genomics
2015-02-19
EGAS00001001165 Genesis of Two Most Prevalent Variants Causing Combined Pituitary Hormone Deficiency in 21 Populations Other
2015-02-19
EGAS00001001167 The Berlin (BLN) panel of glioblastoma cell lines: RNAseq of human gliomasphere cell lines and matched parental tumors Other
2015-02-19
EGAS00001001168 GWAS study on arsenic-exposed population Other
2015-02-20
EGAS00001001170 Recursive splicing in long vertebrate genes Other
2015-02-23
EGAS00001001171 Mutational_Analysis_of_Colorectal_PDX_models Cancer Genomics
2015-02-24
EGAS00001001172 Sequencing of heritable Bleeding and Platelet Disorders Other
2015-02-24
EGAS00001001173 Reference_DNA_standards_for_GCLP_pipeline Cancer Genomics
2015-02-26
EGAS00001001174 Prediction of pigmentation phenotypes by SNP typing in a Northern German population Other
2015-02-26
EGAS00001001176 Study of renal cancers and renal cancer metastases Other
2015-02-27
EGAS00001001178 560 whole-genome sequenced breast cancers Other
2015-03-02
EGAS00001001179 Evolution of DNA repair defects during malignant progression of low-grade gliomas after temozolomide treatment. Other
2015-03-03
EGAS00001001180 Methylation_changes_in_OA_patients_with_chronic_exposure_to_cobalt_and_chromium Population Genomics
2015-03-05
EGAS00001001182 Genome_Diversity_in_Africa_Project___ancient_samples___standard_libraries Population Genomics
2015-03-08
EGAS00001001183 Neuroblastoma relapse trio series from the AMC Other
2015-03-08
EGAS00001001184 Institut Curie Neuroblastoma Whole Genome Sequencing Diagnosis Relapse Other
2015-03-09
EGAS00001001190 Recurrent mTORC1-activating RRAGC mutations in follicular lymphoma Other
2015-03-10
EGAS00001001191 Genome-wide DNA-methylation assessment by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison Other
2015-03-10
EGAS00001001194 Exome sequencing Other
2015-03-12
EGAS00001001195 ICGC Breast Cancer Project Other
2015-03-12
EGAS00001001196 BLUEPRINT DNA methylation profiling of B-cell differentiation using Illumina HumanMethylation 450K BeadArray Other
2015-03-13
EGAS00001001197 BLUEPRINT Gene expression analysis during human B-cell differentiation using the Affymetrix Human Genome U219 Array Other
2015-03-13
EGAS00001001199 MINCR is a MYC-induced lncRNA able to modulate MYC’s transcriptional network in Burkitt lymphoma cells Other
2015-03-20
EGAS00001001202 CONSERTING: integrating copy number analysis with structural variation detection Other
2015-03-24
EGAS00001001203 Pilot_experiment_on_functional_genomics_in_osteoarthritis_RNA Transcriptome Analysis
2015-03-25
EGAS00001001204 G&T-seq: parallel sequencing of the genomes and transcriptomes of single cells Whole Genome Sequencing
2015-03-26
EGAS00001001205 Onco-exaptation of an Endogenous Retroviral LTR Drives IRF5 Expression in Hodgkin Lymphoma Other
2015-03-26
EGAS00001001206 Illumina HumanCoreExome genotyping data from the British Society for Surgery of the Hand Genetics of Dupuytren’s Disease consortium (BSSH-GODD consortium) collection Other
2015-03-27
EGAS00001001207 15x_WGS_HELIC_MANOLIS_ Whole Genome Sequencing
2015-03-27
EGAS00001001209 Anaplastic oligodendroglioma exome and RNA sequencing data Metagenomics
2015-03-27
EGAS00001001210 Whole Genome sequencing of adult T-cell leukemia/lymphoma Other
2015-03-30
EGAS00001001212 Pilot_experiment_on_functional_genomics_in_osteoarthritis Population Genomics
2015-03-30
EGAS00001001213 Pilot_experiment_on_functional_genomics_in_osteoarthritis Population Genomics
2015-03-30
EGAS00001001214 Whole genome and transcriptome analysis of anaplastic thyroid carcinoma Other
2015-04-03
EGAS00001001218 Validation_for_human_early_embryonic_substitutions_ Cancer Genomics
2015-04-10
EGAS00001001219 Deconvolution Other
2015-04-14
EGAS00001001223 LINE_luminal_breast_cancer_Neoadjuvant_Chemotherapy_Study Cancer Genomics
2015-04-15
EGAS00001001231 Yemen_and_Chad_Genotyping Cancer Genomics
2015-04-15
EGAS00001001232 Understanding_Society_GWAS Other
2015-04-16
EGAS00001001234 Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells Other
2015-04-20
EGAS00001001235 Associations between APOE status and cognitive ability across the lifecourse Other
2015-04-21
EGAS00001001236 Comprehensive Transcriptional Analysis of Early Stage Urothelial Carcinoma using whole transcriptome sequencing Other
2015-04-21
EGAS00001001237 SNP genotyping of multiplex autoimmune Addison's families from the UK and Norway Other
2015-04-23
EGAS00001001238 Targeted_replication_of_LVOTO_genes Other
2015-04-23
EGAS00001001240 Exploring the role of mtDNA variation in Multiple Sclerosis in a large cohort of discordant monozygotic twins Metagenomics
2015-04-26
EGAS00001001242 The transcription factor GABP selectively binds and activates the mutant TERT promoter in cancer Other
2015-04-30
EGAS00001001244 Intra-tumor heterogeneity and clonal evolution patterns towards platinum-resistant high-grade serous ovarian cancer Other
2015-05-04
EGAS00001001245 Genomic Epidemiology of Complex Diseases in Population-based Brazilian Cohorts Other
2015-05-04
EGAS00001001247 Papuan Genomes: whole genome sequencing Other
2015-05-07
EGAS00001001250 Exome Sequencing in Moebius Syndrome Other
2015-05-08
EGAS00001001251 Leucocyte eQTLs in autoimmune disease and health Other
2015-05-09
EGAS00001001252 Engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locus Other
2015-05-11
EGAS00001001253 Microinjection_of_hIPSC_derived_intestinal_organoids_with_Salmonella_Typhimurium Transcriptome Analysis
2015-05-13
EGAS00001001254 Tracking the genomic evolution of esophageal adenocarcinoma through neoadjuvant chemotherapy Other
2015-05-13
EGAS00001001255 DNA methylation and somatic mutations converge on cell cycle and define similar evolutionary histories in brain tumors Other
2015-05-13
EGAS00001001256 Genetic_screening__of_GPI_anchor_protein_synthesis__ Other
2015-05-14
EGAS00001001257 Clinical Implications of Genomic Alterations in the Tumor and Circulation of Pancreatic Cancer Patients Other
2015-05-15
EGAS00001001258 Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis Other
2015-05-18
EGAS00001001260 Understand_Paratyphoid_Disease___host_responses_to_human_challenge_with_S__Paratyphi_A Transcriptome Analysis
2015-05-19
EGAS00001001261 Colorectal_Adenoma_Gene_Screen Cancer Genomics
2015-05-19
EGAS00001001262 Deciphering the mutational landscape and the genome organization of LMS Other
2015-05-20
EGAS00001001263 Exome_Sequencing_of_Human_myeloid_malignancies Cancer Genomics
2015-05-20
EGAS00001001264 CMML Collection of WES, WGS, RNA-Seq and ERRBS data Other
2015-05-20
EGAS00001001265 cis-eQTL mapping of human pancreatic islets Metagenomics
2015-05-21
EGAS00001001266 Preeclampsia InterPregGen Consortium: Large-scale GWAS meta-analysis of maternal preclampsia cases and controls from Europe and Central Asia. Plus extension of earlier European fetal preeclampsia GWAS meta-analysis (see EGAS00001001048) by adding Central Asian fetal preeclampsia cases and controls. Datasets provided under this study are GWAS meta-analysis summary statistics and individual level GWAS genotype data. Related InterPregGen Consortium data are also provided under studies EGAS00001000416 and EGAS00001000417 (whole genome sequence data for 100 unrelated Uzbeks and 100 unrelated Kazakhs) and EGAS00001001048 (European fetal preeclampsia GWAS summary statistics and genotype data Other
2015-05-22
EGAS00001001268 Whole exome sequencing of papillary thyroid carcinoma in the Chinese population Other
2015-05-25
EGAS00001001272 HipSci HumanExome BeadChip analysis-Rare_BBS Other
2015-06-04
EGAS00001001273 HipSci HumanExome BeadChip analysis - monogenic diabetes Other
2015-06-04
EGAS00001001274 HipSci Illumina 450K Methylation analysis-Rare_BBS Other
2015-06-04
EGAS00001001275 HipSci Illumina 450K Methylation analysis - monogenic diabetes Other
2015-06-04
EGAS00001001276 HipSci HumanHT 12v4 Expression BeadChip analysis-Rare_BBS Other
2015-06-04
EGAS00001001277 HipSci HumanHT 12v4 Expression BeadChip analysis - monogenic diabetes Other
2015-06-04
EGAS00001001279 Novel Epigenetic Markers for Toxicity after Intraoperative and Conventional Radiotherapy for Breast Cancer Other
2015-06-06
EGAS00001001281 PLCG1 R707Q mutation is counter selected under targeted therapy in a patient with a hepatic angiosarcoma Other
2015-06-08
EGAS00001001283 IL_10_signalling_and_macrophage_gene_expression Transcriptome Analysis
2015-06-09
EGAS00001001284 Recurrent adeno-associated virus 2-related insertional mutagenesis in human hepatocellular carcinomas Other
2015-06-09
EGAS00001001285 Ribosome_Profiling_of_Macrophages_during_Salmonella_Infection Whole Genome Sequencing
2015-06-10
EGAS00001001287 BLUEPRINT DNA methylation profiles of graft donors in allogenic hematopoietic stem cell transplantation Other
2015-06-12
EGAS00001001288 Induced Pluripotent Cells Derived from Differentiated Rod Photoreceptors Undergo Efficient Retinogenesis in Three-Dimensional Cultures Other
2015-06-12
EGAS00001001289 Targeted_Sequencing_of_Human_Myeloid_Malignancies Cancer Genomics
2015-06-17
EGAS00001001292 SNP genotyping data in genes related to trace element homeostasis Other
2015-06-19
EGAS00001001293 Growth Hormone (GH) -secreting Pituitary Adenoma Other
2015-06-22
EGAS00001001294 Transcriptome_human_nasal_epithelium Transcriptome Analysis
2015-06-22
EGAS00001001296 Integrated molecular analysis of adult T-cell leukemia/lymphoma Other
2015-06-22
EGAS00001001297 Comprehensive analysis of the (epi)genome of pediatric atypical teratoid/rhabdoid tumours (AT/RTs) Other
2015-06-23
EGAS00001001299 Multiple_Myeloma_Diagnosis_to_Relapse_study_samples Cancer Genomics
2015-06-25
EGAS00001001301 PRDM9_loss_of_function_follow_up_from_Born_in_Bradford_Autozygosity_sequencing Whole Genome Sequencing
2015-06-25
EGAS00001001302 Identification of four new susceptibility loci for testicular germ cell tumour, including variants near GAB2, GSPT1 and ZFPM1 Other
2015-06-30
EGAS00001001303 Accurate sample assignment in a multiplexed, ultra-sensitive, high-throughput sequencing assay for minimal residual disease Other
2015-06-30
EGAS00001001304 Resistance_to_MAPK_inhibitor_induces_internal_duplication_in_BRAF Other
2015-07-01
EGAS00001001305 The Genomic Landscape of Response to EGFR Blockade in Colorectal Cancer Other
2015-07-01
EGAS00001001306 Integrated Genomic Analysis of Chronic Lymphocytic Leukaemia Other
2015-07-02
EGAS00001001308 Telomerase activation by genomic rearrangements in high-risk neuroblastoma Other
2015-07-06
EGAS00001001310 Barcoding reveals complex clonal dynamics of de novo transformed human mammary cells Other
2015-07-09
EGAS00001001311 Genome-wide study of resistance to severe malaria in eleven worldwide populations Other
2015-07-13
EGAS00001001314 Genetic landscape of pediatric ETV6-RUNX1 acute lymphoblastic leukemia Other
2015-07-20
EGAS00001001315 Genetic landscape of pediatric ETV6-RUNX1 acute lymphoblastic leukemia Other
2015-07-20
EGAS00001001316 Genetic landscape of pediatric high hyperdiploid acute lymphoblastic leukemia Other
2015-07-20
EGAS00001001317 Genomic landscape of childhood acute lymphoblastic leukemia Other
2015-07-21
EGAS00001001318 HipSci___RNAseq___Rare_BBS Transcriptome Analysis
2015-07-22
EGAS00001001323 Whole_Genome_Sequencing_of_JK_Family Whole Genome Sequencing
2015-07-23
EGAS00001001324 JMML targeted sequencing (2013) Other
2015-07-23
EGAS00001001329 Carcinoma of the oral tongue (OTSCC) genomic landscape characterisation Other
2015-07-27
EGAS00001001332 A collection of 142 samples used to evaluate the sensitivity and specificity of small-scale variation detection in exome-capture data with a particular focus on indel detection. Other
2015-07-27
EGAS00001001340 Genomic analysis of HPV positive versus HPV negative esophageal adenocarcinoma Other
2015-07-29
EGAS00001001343 Somatic_Genetics_of_lesions_from_a_POT1_patient Cancer Genomics
2015-07-30
EGAS00001001348 Melanoma_multi_site_metastases Cancer Genomics
2015-07-31
EGAS00001001353 Independent development of lymphoid and histiocytic malignancies from a shared early precursor Other
2015-08-03
EGAS00001001354 Genome-wide association data on male-pattern baldness Other
2015-08-03
EGAS00001001355 Whole_Genome_Sequencing_of_INTERVAL Whole Genome Sequencing
2015-08-03
EGAS00001001382 OCCAMS_Oesophageal_Cancer_Organoids_1 Cancer Genomics
2015-08-06
EGAS00001001385 A somatic reference standard for cancer genome sequencing with COLO829 Other
2015-08-06
EGAS00001001386 Novel genes for Intellectual Disability identified using whole genome sequence and pathway analysis Other
2015-08-06
EGAS00001001387 Genomes of Relapsing Neuroblastoma Other
2015-08-10
EGAS00001001394 Genome-wide identification of distinct miRNA-mRNA target regulation pairs in Non-Hodgkin lymphomas: a report from the ICGC MMML-Seq consortium Other
2015-08-13
EGAS00001001418 Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis Other
2015-08-19
EGAS00001001422 Precursor_lesions__clonal_architecture_and_relapse_in_Wilms_nephroblastoma Cancer Genomics
2015-08-20
EGAS00001001427 Trans-ethnic genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation Other
2015-08-25
EGAS00001001429 Congenital_anosmia_2 Other
2015-08-26
EGAS00001001431 Breast Cancer - Subtype defined by an amplification of the HER2 gene Other
2015-08-28
EGAS00001001433 Fixative optimisation study for BRITROC project Other
2015-08-28
EGAS00001001436 Multiregion Whole Exome sequencing of paediatric High Grade Gliomas and DIPG Other
2015-09-01
EGAS00001001437 Chromatin immunoprecipitation linked to next-generation whole genome sequencing (ChIP-Seq) for H3K36me3 in paediatric high grade glioma cell lines KKNS4 and SF188 with and without a G34V mutation in H3F3A Other
2015-09-01
EGAS00001001456 BLUEPRINT EpiVar 450K DNA methylation profiles of naive CD4+ T-cells, monocytes & neutrophils Other
2015-09-04
EGAS00001001457 Genetic and epigenetic characterization of adenoid cystic carcinoma Other
2015-09-04
EGAS00001001458 GENETIC HISTORY OF ITALY Other
2015-09-08
EGAS00001001459 GoT2D: Genetics of Type 2 Diabetes, a study of the the genetic architecture of type 2 diabetes using low pass whole genome sequencing and high density SNP genotyping in 2,657 individuals. Other
2015-09-08
EGAS00001001460 T2D-GENES: Exome sequencing Other
2015-09-08
EGAS00001001461 Inherited damaging mutations in immune-related genes favour the development of genetically heterogeneous synchronous colorectal cancer. Other
2015-09-09
EGAS00001001462 Targeting PTPRK-RSPO3 colon tumours promotesdifferentiation and loss of stem-cell function Other
2015-09-09
EGAS00001001463 Exome-sequencing of human B cell lymphoma cell lines Other
2015-09-10
EGAS00001001465 HipSci - Human Induced Pluripotent Stem Cells Initiative Other
2015-09-11
EGAS00001001466 Sequencing of serial plasma and multiregional tumor samples in a patient with metastatic breast cancer Other
2015-09-12
EGAS00001001472 Analysis of the lung gene expression profile in COPD Other
2015-09-18
EGAS00001001473 Whole genome and transcriptome analysis of medullary thyroid cancer Other
2015-09-18
EGAS00001001474 WGS-Lung Cancer sample 30 pair Other
2015-09-20
EGAS00001001475 71 Whole-exome sequencing of Esophageal Squamous Cell Carcinoma on Chinese Patients Other
2015-09-20
EGAS00001001476 TraIT Cell Line use case Other
2015-09-21
EGAS00001001479 TERT rearrangements are frequent in neuroblastoma and identify aggressive tumors Other
2015-09-28
EGAS00001001486 Transcriptomics_of_human_olfactory_mucosa Transcriptome Analysis
2015-09-29
EGAS00001001487 Whole-genome sequencing in 14 cases and whole-exome sequencing in 90 cases of Chinese ESCC Other
1980-01-01
EGAS00001001501 TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism Other
1980-01-01
EGAS00001001515 The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north-south gradient among Europeans Other
2015-09-30
EGAS00001001516 Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study Other
2015-09-30
EGAS00001001519 Glioblastoma_CRISPR_Screen Cancer Genomics
1980-01-01
EGAS00001001520 BAP1_sequence_of_uveal_melanoma_cell_lines Cancer Genomics
1980-01-01
EGAS00001001521 S_CORT_Stratification_in_COloRecTal_cancer_ Cancer Genomics
2015-10-01
EGAS00001001537 RNA_expression_profiling_of_melanoma_patient_derived_xenograft Transcriptome Analysis
1980-01-01
EGAS00001001539 A comprehensive assessment of somatic mutation detection in cancer using whole genome sequencing Other
1980-01-01
EGAS00001001540 Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma Other
1980-01-01
EGAS00001001542 Whole exome sequencing of germline DNA was performed and subsequent polymorphisms in genes known and putatively involved in the innate immune response to fungi were identified Other
2015-10-07
EGAS00001001552 Whole genome sequencing of primary and metastatic Melanoma cases in an Australian cohort. Other
2015-10-09
EGAS00001001553 Genetic landscape of relapsed DLBCL Other
2015-10-10
EGAS00001001558 APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UGWAS component) Other
2015-10-12
EGAS00001001559 AML_WES Other
2015-10-14
EGAS00001001561 PSCP_mutation_analysis_in_hESCs Whole Genome Sequencing
2015-10-16
EGAS00001001563 Genomic characterization of Malignant Pleural Mesothelioma. Other
1980-01-01
EGAS00001001565 The_British_Autozygosity_Populations_BioResource Other
2015-10-19
EGAS00001001568 reChIP-seq reveals widespread bivalency of H3K4me3 and H3K27me3 in CD4+ memory T-Cells Other
1980-01-01
EGAS00001001569 Population whole-genome bisulfite sequencing across two tissues highlights environment as principal source of human methylome variation Other
1980-01-01
EGAS00001001570 Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015 Other
2015-10-24
EGAS00001001572 Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing Other
2015-10-28
EGAS00001001573 The_genetic_evolution_of_precursor_lesions_in_pancreatic_cancer Cancer Genomics
1980-01-01
EGAS00001001575 Prenatal lead exposure is associated with decreased cord blood DNA methylation of the glycoprotein VI gene involved in platelet activation and thrombus formation Other
2015-10-30
EGAS00001001585 Genotype and exome data for an Australian Aboriginal population: a reference panel for health-based research Other
1980-01-01
EGAS00001001587 Papuan_Genotyping Population Genomics
2015-11-03
EGAS00001001588 Integrated genomic characterization of IDH1 mutant Glioma malignant progression Other
1980-01-01
EGAS00001001590 TTV018_RORC_IBD_associated_genotype_effects_on_RORgT_expression_and_function_in_ex_vivo_T_cells Transcriptome Analysis
1980-01-01
EGAS00001001591 RNAseq_of_ribosomal_footprints Cancer Genomics
1980-01-01
EGAS00001001595 Epigenetic dynamics of monocyte to macrophage differentiation Other
1980-01-01
EGAS00001001596 BLUEPRINT ATAC-seq data for cells in the haematopoietic lineages, from adult and cord blood samples Other
1980-01-01
EGAS00001001597 Low_depth_whole_genome_sequencing_across_multiple_isolated_populations Whole Genome Sequencing
1980-01-01
EGAS00001001598 BLUEPRINT DNA methylation profiles of monocytes, T cells and B cells in type 1 diabetes-discordant monozygotic twins Other
2015-11-10
EGAS00001001599 A genetic compendium of human brains from the UK Medical Research Council brain tissue resource Other
2015-11-11
EGAS00001001600 Container Study for ICGC Malignant Lymphoma Master Study (MMML) Other
2015-11-12
EGAS00001001601 Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes Other
1980-01-01
EGAS00001001603 The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma Other
2015-11-19
EGAS00001001604 Identifying_new_diagnostic_and_treatment_pathways_for_patients_with_unclassifiable_sarcomas Cancer Genomics
2015-11-19
EGAS00001001605 Targeted sequencing of 12 genes in patients with HLH Other
1980-01-01
EGAS00001001606 Homozygous loss-of-function variants in European cosmopolitan and isolate populations Other
1980-01-01
EGAS00001001607 Targeted sequencing of brain expressed miRNA genes Other
1980-01-01
EGAS00001001608 All available datasets of DEEP Other
1980-01-01
EGAS00001001610 We screened 2.5 million SNPs in 161 individuals from 13 Sahelian populations from Western, Central and Eastern parts of the belt, and including both nomadic and sedentary groups Other
2015-11-24
EGAS00001001611 FetalQuant-SD: Accurate quantification of fetal DNA fraction by shallow-depth sequencing of maternal plasma DNA Other
2015-11-26
EGAS00001001612 Exome sequencing of uterine leiomyosarcomas Other
2015-11-26
EGAS00001001613 GILD_ExomeSeq_PTNHL Cancer Genomics
2015-11-26
EGAS00001001614 Melanoma_C32_ENU_resistance_to_Combination_Therapy Cancer Genomics
2015-11-26
EGAS00001001615 MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers Other
2015-11-27
EGAS00001001623 Pediatric Whole Genome Sequencing Diagnostic Utility Other
2015-12-01
EGAS00001001624 Epigenetic profiling of human CD4+ memory T cells reveals their proliferative history and argues in favor of a progressive differentiation model driven by epigenetically controlled master regulators. Other
2015-12-02
EGAS00001001625 PSCP_bisulphite_analysis_in_hESCs Epigenetics
2015-12-03
EGAS00001001632 New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs Other
2015-12-08
EGAS00001001637 BLUEPRINT DNA Methylation 450K data of mantle cell lymphoma Other
2015-12-16
EGAS00001001638 BLUEPRINT Bisulfite-seq and Whole Genome Sequencing of mantle cell lymphoma Other
2015-12-16
EGAS00001001639 Amplicon_based_sequencing_of_drug_resistant_organoids Cancer Genomics
2015-12-16
EGAS00001001641 BLUEPRINT Epigenetic characterization of megakaryocytes and erythroblasts Other
2015-12-17
EGAS00001001645 EXOME-WIDE ASSOCIATION ANALYSIS OF CORONARY ARTERY DISEASE IN THE KINGDOM OF SAUDI ARABIA POPULATION Other
2015-12-18
EGAS00001001653 Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma Other
2015-12-21
EGAS00001001654 Spatial and Temporal Homogeneity of Driver Mutations in Diffuse Intrinsic Pointine Glioma Other
2015-12-21
EGAS00001001655 RNA_seq_analysis_of_transcriptome_variation_with_human_ESC_subclones Transcriptome Analysis
2015-12-22
EGAS00001001656 A unidirectional histone code in bidirectional promoters across cell types Other
2015-12-22
EGAS00001001658 33 patients with Monoclonal Gammopathy of Undetermined Significance (MGUS) had whole exome sequencing performed. Cells were sorted by FACSAria using CD138, CD19 and CD56 to obtain a pure abnormal plasma cell population. Generated somatic variants were compared to a previous study of 463 multiple myeloma patients. Other
2015-12-28
EGAS00001001659 Integrated clinical, whole genome, and transcriptome analysis of multisampled lethal metastatic prostate cancer Other
2016-01-01
EGAS00001001663 Population Structure and Genetic Diversity in Argentinean populations Other
2016-01-07
EGAS00001001664 Investigating_the_genetics_of_immunity_against_Salmonella_in_humans Whole Genome Sequencing
2016-01-07
EGAS00001001665 Rare SNPs in receptor tyrosine kinases are negative outcome predictors in multiple myeloma Other
2016-01-07
EGAS00001001666 Large scale familial CRC exome sequencing study Other
2016-01-08
EGAS00001001667 ICR MOPOPGEN UK exome control series Other
2016-01-08
EGAS00001001675 Amplicon_based_sequencing_of_drug_resistant_lung_cancer_cell_lines Cancer Genomics
2016-01-13
EGAS00001001676 Clonal_architecture_of_pre_malignant_and_malignant_tumours Cancer Genomics
2016-01-15
EGAS00001001678 Comparison of HCC cell lines and primary HCCs Other
2016-01-19
EGAS00001001682 Tissue-specific mutation accumulation in human adult stem cells during life Other
2016-01-20
EGAS00001001686 Paired exome analysis in urothelial carcinoma Other
2016-01-21
EGAS00001001687 Clonal_expansion_of_mutated_cell_population_in_bladder_urothelium_ Cancer Genomics
2016-01-22
EGAS00001001688 Genome_Diversity_in_Africa_Project__Benin Whole Genome Sequencing
2016-01-25
EGAS00001001689 Flemish_Gut_Flora_Project Other
2016-01-25
EGAS00001001690 Whole exome sequencing on primary retinoblastoma tissues and matching lymphocyte DNA. Other
2016-01-26
EGAS00001001692 ICGC PanCancer Analysis of Whole Genomes Cancer Genomics
2016-01-29
EGAS00001001694 Automated system for scoring hematoxylin and eosin-stained ovarian cancer sections by identifying single cells uncovered that stromal cell ratio is a significant predictor for overall survival and progression-free survival. Other
2016-02-01
EGAS00001001695 Whole-exome sequencing of breast cancer metastasis and corresponding blood samples Other
2016-02-02
EGAS00001001697 Melanoma_C32_ENU_Resistance_to_Single_Agent_Therapy Cancer Genomics
2016-02-03
EGAS00001001698 Warm_Autopsy_Single_Cell_X10 Cancer Genomics
2016-02-03
EGAS00001001699 Genetic sequencing of MODY patients. Other
2016-02-03
EGAS00001001700 Post-zygotic germline mutations in sperm Other
2016-02-04
EGAS00001001701 Very short reads file for testing purposes Other
2016-02-05
EGAS00001001702 Patient-derived conditionally reprogrammed cells (CRCs) were established and characterized to assess their biological properties and to apply these to test the efficacies of drugs. Other
2016-02-06
EGAS00001001704 LifeLines-DEEP population multi-omix cohort from the noth of the Netherlands. Other
2016-02-08
EGAS00001001706 Identification of gene mutations and fusion genes in patients with Sézary Syndrome Other
2016-02-08
EGAS00001001708 RNA_seq_of_Toxoplasma_gondii_response_in_human_macrophages Transcriptome Analysis
2016-02-10
EGAS00001001709 Histological Transformation and Progression in Follicular Lymphoma: a Clonal Evolution Study Other
2016-02-10
EGAS00001001710 The Haplotype Reference Consortium Other
2016-02-10
EGAS00001001711 Korean Young Age Diffuse Gastric Cancers Other
2016-02-11
EGAS00001001713 PAGE: Prenatal Assessment of Genomes and Exomes Other
2016-02-11
EGAS00001001714 WES analysis of a mixed cohort of pituitary tumors Other
2016-02-12
EGAS00001001715 Copy number profiling of primary samples and cell lines of retinoblastoma Other
2016-02-12
EGAS00001001723 Genomic characterization of esophageal squamous cell carcinoma reveals critical genes underlying tumorigenesis and poor prognosis Other
2016-02-16
EGAS00001001726 HipSci whole exome sequencing for embryonic stem cell control lines Other
2016-02-19
EGAS00001001727 HipSci RNA sequencing for embryonic stem cell control lines Other
2016-02-19
EGAS00001001728 HipSci Methylation analysis for embryonic stem cell control lines Other
2016-02-19
EGAS00001001729 HipSci expression microarray for embryonic stem cell control lines Other
2016-02-19
EGAS00001001730 HipSci genotyping microarray for embryonic stem cell control lines Other
2016-02-19
EGAS00001001732 Novel mutational mechanisms and drivers in Pancreatic Neuroendocrine Tumours Other
2016-02-22
EGAS00001001733 120 individuals from the TEENAGE study (Ntalla et al., 2013) have been genotyped on the Illumina HumanCoreExome-12v1-1_A array. This is a population-based study of adolescents from the Attica region in Greece Other
2016-02-22
EGAS00001001735 IBD_Whole_Genome_Sequencing_Phase_1 Other
2016-02-22
EGAS00001001736 Elucidating the genomic architecture of Asian EGFR-mutant lung adenocarcinoma through multi-region exome sequencing Other
2016-02-24
EGAS00001001737 Exome-sequencing of two UFM individuals and their Fragile X family members. Other
2016-02-25
EGAS00001001738 Multi-layered population structure in Island Southeast Asians Other
2016-02-27
EGAS00001001740 Nrf2 transcript alterations Other
2016-02-27
EGAS00001001741 Searching for variants associated with endometriosis Other
2016-03-02
EGAS00001001742 We performed whole exome sequencing (WES) using Hiseq on 22 paired CMLs. We also performed whole exome sequencing (WES) using CG on 88 paired CMLs. All the data belongs to CML in China - ICGC project. Other
2016-03-02
EGAS00001001743 ENU_CCK_81_cetuximab_pilot_project Cancer Genomics
2016-03-02
EGAS00001001744 ENU_NCI_H508_cetuximab_fixed_concentration_project Cancer Genomics
2016-03-02
EGAS00001001745 ENU_NCI_H508_Cetuximab_SecondRound Cancer Genomics
2016-03-02
EGAS00001001746 Drug-perturbation-based stratification of blood cancer Other
2016-03-03
EGAS00001001751 An integrative model of pathway convergence in genetically heterogeneous blast crisis chronic myeloid leukemia (CML) Other
2016-03-10
EGAS00001001752 Dissection of the molecular complexity of colorectal cancer in pre-clinical models identifies predictive signatures of sensitivity to EGFR inhibitors Other
2016-03-11
EGAS00001001753 METABRIC: Data from Pereira et al (2016), The somatic mutation profiles of 2433 breast cancers refine their genomic and transcriptomic landscapes. Nat Comms 7. Other
2016-03-13
EGAS00001001754 Inferring expressed genes by whole-genome sequencing of plasma DNA Other
2016-03-14
EGAS00001001755 Transcriptomes_of_human_lymphocytes Transcriptome Analysis
2016-03-15
EGAS00001001756 WTCCC2 Bacteraemia Susceptibility (BS) samples Other
2016-03-22
EGAS00001001757 Evolutionary Genome Analysis of Transformation into Small Cell Carcinomas from Lung Adenocarcinomas Other
2016-03-22
EGAS00001001763 Longitudinal RNA-seq (whole blood) in a twin cohort Other
2016-03-30
EGAS00001001764 The_mutational_landscape_of_recurrent_Glioblastome_multiforme Cancer Genomics
2016-03-30
EGAS00001001765 Targeted_analysis_of_chondrosarcoma_cancer_genes Cancer Genomics
2016-03-30
EGAS00001001766 A Genomic History of Aboriginal Australia Other
2016-03-30
EGAS00001001767 Ashkenazi Jewish Leukoencephalopathy Exome Sequencing
2016-03-30
EGAS00001001774 Korea Epigenome Project(KEP), Korea National Research Institute of Health(KNIH) Other
2016-04-04
EGAS00001001777 ENU_LS_411N_TripleTherapy Cancer Genomics
2016-04-12
EGAS00001001778 ENU_HT_29_BRAF_Triple_Therapy_Clones Cancer Genomics
2016-04-12
EGAS00001001779 AML clonal phylogeny Other
2016-04-13
EGAS00001001780 V2_panel_bait_design_test Cancer Genomics
2016-04-14
EGAS00001001782 Mitochondrial-Nuclear Mutational Cross-Talk Drives Recurrence of Localized Prostate Cancer Other
2016-04-14
EGAS00001001783 Genome sequencing of HCC from a Chinese cohort Other
2016-04-15
EGAS00001001784 Analysis of tumor periphery and center-specific mutations in renal cell carcinoma Other
2016-04-19
EGAS00001001788 Genomic Profiling of Thyroid Cancer Reveals a Role for Thyroglobulin in Metastasis Other
2016-04-24
EGAS00001001789 Rare disruptive mutations in ciliary function genes contribute to testicular cancer susceptibility Other
2016-04-25
EGAS00001001791 ZhongShan Hospital liver tumor single cell sequencing. Other
2016-04-27
EGAS00001001795 RNA-sequencing data from 195 B-cell precursor acute lymphoblastic leukemias and mate pair whole genome sequencing data from 15 B-cell precursor acute lymphoblastic leukemias Other
2016-04-27
EGAS00001001797 Targeted_gene_screen_of_drug_resistant_organoids Cancer Genomics
2016-04-29
EGAS00001001799 Spiradenocarcinoma Cancer Genomics
2016-04-29
EGAS00001001800 Spatio-temporal evolution of the primary glioblastoma genome (newly added after 2015) Other
2016-05-01
EGAS00001001801 Comparing nodal versus bony metastatic spread using tumour phylogenies Other
2016-05-04
EGAS00001001802 Native_American_Ancient_DNA_sequencing Whole Genome Sequencing
2016-05-05
EGAS00001001803 Characterization of a human iPSC-derived endocrine pancreas model Other
2016-05-05
EGAS00001001804 Interactions between the tumor and the systemic response of breast cancer patients Other
2016-05-06
EGAS00001001805 A novel TP53-KPNA3 translocation defines a de novo treatment-resistant clone in osteosarcoma Other
2016-05-09
EGAS00001001806 V2_Colorectal_panel_test Cancer Genomics
2016-05-10
EGAS00001001807 V4_Colorectal_panel_test Cancer Genomics
2016-05-10
EGAS00001001808 V4_panel_bait_design_test Cancer Genomics
2016-05-10
EGAS00001001810 Clonal selection and double hit events involving tumor suppressor genes underlie relapse from total therapy Other
2016-05-10
EGAS00001001821 Epigenome and transcriptome profiling of chronic lymphocytic leukemia patients Other
2016-05-11
EGAS00001001822 QSEA – modelling of genome-wide DNA methylation from sequencing enrichment experiments Other
2016-05-12
EGAS00001001828 Genome_Diversity_in_Africa_Project___GemCode_libraries_ Population Genomics
2016-05-13
EGAS00001001835 Whole exome sequencing of Finnish hereditary breast cancer families Other
2016-05-17
EGAS00001001836 Identification of 19 novel loci reveals gene regulatory mechanisms determining susceptibility to testicular germ cell tumour Other
2016-05-17
EGAS00001001837 Dense_fine_mapping_study_identifies_new_susceptibility_loci_for_primary_biliary_cirrhosis Population Genomics
2016-05-18
EGAS00001001838 Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing Other
2016-05-18
EGAS00001001839 Circulating Tumor DNA Analysis Detects Minimal Residual Disease and Predicts Recurrence in Patients with Stage II Colon Cancer Other
2016-05-18
EGAS00001001840 RNA-seq analysis of megakaryocytes and granulocytes in Quebec platelet disorder Other
2016-05-18
EGAS00001001841 The dataset of Southeast Borneo individuals (Banjar and Ngaju ethnic groups) was used as comparative data to determine the Asian parental population of the Malagasy. Our study found strong support for an origin of the Asian ancestry of Malagasy among the Banjar. Other
2016-05-19
EGAS00001001844 Targeting FGFR1 for treatment of soft-tissue sarcoma (H021) Other
2016-05-23
EGAS00001001845 Mutant KIT as imatinib-sensitive target in metastatic sinonasal carcinoma (H021) Other
2016-05-23
EGAS00001001846 Integration of genomics and histology reveals diagnosis and effective therapy of refractory cancer of unknown primary with PDL1 amplification (H021) Other
2016-05-23
EGAS00001001847 Genomic and transcriptional landscape of P2RY8-CRLF2-positive childhood acute lymphoblastic leukemia Other
2016-05-23
EGAS00001001848 Evolution of a FLT3-TKD mutated subclone at meningeal relapse in acute promyelocytic leukemia (H021) Other
2016-05-23
EGAS00001001849 Whole-genome sequencing of two probands with hereditary spastic paraplegia reveals novel splice-donor region mutation and known pathogenic mutation in SPG11 Other
2016-05-25
EGAS00001001852 Population_sequencing_phasing Population Genomics
2016-05-26
EGAS00001001853 Australia_and_New_Guinea_haplotype_phasing_ Population Genomics
2016-05-26
EGAS00001001854 Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH1 Other
2016-05-26
EGAS00001001855 Low_input_LC__WGS_ Other
2016-05-27
EGAS00001001856 Low_input_LC__ISC_ Cancer Genomics
2016-05-27
EGAS00001001857 Genetic subclone heterogeneity of tumor-initiating cells in human colorectal cancer Other
2016-05-29
EGAS00001001858 Whole transcriptome and exome sequencing of childhood ALL Other
2016-05-31
EGAS00001001859 Transcriptome profiling for Korean Diffuse Gastric cancers Other
2016-06-01
EGAS00001001861 Molecular evolution of metastatic clear cell renal cell carcinoma progressing under tyrosine kinase inhibitor therapy (HIPO-045) Other
2016-06-01
EGAS00001001862 Recurrent somatic JAK-STAT mutations within a novel RUNX1-mutated pedigree Other
2016-06-01
EGAS00001001866 Subtype specific progression from DCIS to invasive breast cancer Other
2016-06-07
EGAS00001001868 Recent genetic history of Denmark Other
2016-06-08
EGAS00001001870 CD4+ T cell subsets stratified by complement receptor type 2 (CR2) expression Other
2016-06-10
EGAS00001001871 Multi-omics analysis of primary glioblastoma cell-lines shows recapitulation of pivotal molecular features of parental tumors Other
2016-06-21
EGAS00001001872 RNA sequencing data from visceral and abdominal subcutaneous adipose tissue from morbidly obese women with normal glucose tolerance or type 2 diabetes Other
2016-06-21
EGAS00001001873 Transcriptome_analysis_of_anaplastic_meningiomas Transcriptome Analysis
2016-06-14
EGAS00001001874 Mutant_clone_mapping_in_normal_oesophagus Cancer Genomics
2016-06-14
EGAS00001001875 Variation in the Glucose Transporter gene SLC2A2 is associated with glycaemic response to metformin Other
2016-06-21
EGAS00001001876 Exome and RNA sequencing of relapsed TCF3-PBX1 t(1;19) acute lymphoblastic leukemia Other
2016-06-19
EGAS00001001878 Non-Mendalian inheritance of extrachromosal DNA elements can drive disease evolution in glioblastoma Other
2016-06-21
EGAS00001001879 EATL-II STUDY Other
2016-06-22
EGAS00001001880 Spatiotemporal genomic architecture informs precision oncology in glioblsatoma Other
2016-06-23
EGAS00001001881 Investigating genetic susceptibility to rheumatic heart disease in Oceania Other
2016-06-23
EGAS00001001882 Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends Other
2016-06-24
EGAS00001001883 Resolving_the_Genetic_Architecture_of_Aseptic_Loosening_After_Total_Hip_Replacement Population Genomics
2016-06-27
EGAS00001001886 We performed an integrative analysis to determine genomic aberrations common to sporadic schwannomas. Other
2016-06-28
EGAS00001001889 Whole exome sequencing data of germline and two independent primary leukemias of five patients Other
2016-06-30
EGAS00001001891 ORCADES_15x Whole Genome Sequencing
2016-07-04
EGAS00001001892 Inactivation of TGFβ receptors in stem cells drives cutaneous squamous cell carcinoma - 30 whole exomes Other
2016-07-04
EGAS00001001893 The molecular landscape of colorectal cancer reveals genetic mutations. Other
2016-07-06
EGAS00001001895 Genetic control of the transcriptomic response of monocytes to bacterial and viral stimuli assessed by RNA-seq in Africans and Europeans Other
2016-07-06
EGAS00001001896 Molecular dissection of germline chromothripsis in a developmental context Other
2016-07-07
EGAS00001001897 Integrated Molecular Profilting in Advanced Cancers Trial Other
2016-07-07
EGAS00001001898 The Prediction and Prevention of Preeclampsia Other
2016-07-08
EGAS00001001899 Knee_OA_Functional_Genomics Transcriptome Analysis
2016-07-11
EGAS00001001900 Comparison of EGF and PDGF driven glioblastomas. Other
2016-07-12
EGAS00001001901 Whole Genome Sequencing of Gingivo-buccal Cancer: ICGC-India Project_YR03 Other
2016-07-13
EGAS00001001906 SNU_WGS_AML Other
2016-07-18
EGAS00001001908 Breast Cancer - Very young women Other
2016-07-19
EGAS00001001909 Premalignant SOX2 overexpression in the fallopian tubes of ovarian cancer patients: Discovery and validation studies Other
2016-07-20
EGAS00001001910 Novel regional age-associated DNA methylation changes within human common disease-associated loci Other
2016-07-24
EGAS00001001911 Lineage-specific genome architecture links disease variants to target genes Other
2016-07-24
EGAS00001001913 Breast Cancer PDTX Encyclopaedia Other
2016-07-24
EGAS00001001914 Maastricht IBS cohort MIBS Other
2016-07-27
EGAS00001001916 Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas Other
2016-07-30
EGAS00001001918 RNA sequencing in blood samples of cluster headache patients Other
2016-08-02
EGAS00001001922 DNA methylation and the adverse metabolic outcomes of adiposity Other
2016-08-02
EGAS00001001923 Deregulation of DUX4 and ERG in acute lymphoblastic leukemia Other
2016-08-06
EGAS00001001924 MIBS MGS Other
2016-08-04
EGAS00001001926 Mesenchymal inflammation drives genotoxic stress in hematopoietic stem cells and predicts disease evolution in human pre-leukemia Other
2016-08-06
EGAS00001001930 Hi-C dataset for testicular germ cell tumour GWAS risk loci, as described in the Oncoarray Litchfield et al. 2016 paper. Other
2016-08-09
EGAS00001001933 Mutant_clone_mapping_in_normal_oesohagus_and_skin Other
2016-08-09
EGAS00001001934 Genomic characterization of NUT midline carcinoma Other
2016-08-09
EGAS00001001937 IHEC DEEP Release August 2016 Other
2016-08-12
EGAS00001001940 Impact of mutational profiles on response of primary oestrogen receptor-positive breast cancers to oestrogen deprivation Other
2016-08-15
EGAS00001001941 Evolution_of_the_cancer_epigenome_in_myeloproliferative_neoplasms_ Cancer Genomics
2016-08-18
EGAS00001001943 Histone Acetylome-wide Association Study of Autism Spectrum Disorder Other
2016-08-24
EGAS00001001945 Single cell Transcriptomic Analysis of Cellular Heterogeneity in Human Colorectal Tumors Other
2016-08-25
EGAS00001001946 CRC Promoter capture Hi-C Other
2016-08-26
EGAS00001001948 Exome sequencing of samples taken at multipl time points to monitor therapy response in AML Other
2016-09-01
EGAS00001001949 Targeted sequencing analysis for MDS with HSCT Other
2016-09-01
EGAS00001001950 Mutational landscape of renal cell carcinoma with venous tumor thrombus Other
2016-09-01
EGAS00001001951 Molecular analysis of circulating tumour cells identifies distinct profiles in chemosensitive and chemorefractory patients with small cell lung cancer Other
2016-09-05
EGAS00001001952 Genomic Analyses Identify Recurrent MEF2D Fusions in Acute Lymphoblastic Leukemia Other
2016-09-06
EGAS00001001953 Comprehensive molecular profiling identifies novel genetic drivers and subtypes underlying medulloblastoma Other
2016-09-06
EGAS00001001954 Genomics of enteropathy associated T cell lymphoma (EATL) Other
2016-09-06
EGAS00001001957 Relaxed selection during a recent human expansion Other
2016-09-09
EGAS00001001959 The Simons Genome Diversity Project: 300 genomes from 142 diverse populations Other
2016-09-12
EGAS00001001960 Novel CNV contribution to schizophrenia from a genome wide study of 41,321 subjects Other
2016-09-13
EGAS00001001961 Chromosome contacts in activated T cells identify autoimmune disease-candidate genes Other
2016-09-13
EGAS00001001963 CLL_targeted_exome_sequencing Cancer Genomics
2016-09-13
EGAS00001001964 The_contribution_of_POT1_variants_to_sporadic_melanoma_development Cancer Genomics
2016-09-14
EGAS00001001967 FFPE_whole_genome_pilot Cancer Genomics
2016-09-15
EGAS00001001968 Metastatic_Breast_Cancer_Validation Cancer Genomics
2016-09-15
EGAS00001001969 Whole genome sequencing of colon organoid cultures with artificially induced oncogenic mutations Other
2016-09-16
EGAS00001001971 In_Situ_Transcription_whole_genome_sequencing Cancer Genomics
2016-09-20
EGAS00001001972 Breast_Heterogeneity_Validation Cancer Genomics
2016-09-20
EGAS00001001973 Exome sequence data for germline, primary tumor, and relapse tumor of a transformed non-Hodgkins lymphoma patient with unexpected long-time remission Other
2016-09-20
EGAS00001001974 HipSci___Whole_Exome_sequencing___Alport Other
2016-09-20
EGAS00001001975 HipSci___Whole_Exome_sequencing___Battens Other
2016-09-20
EGAS00001001976 HipSci___Whole_Exome_sequencing___BPD Other
2016-09-20
EGAS00001001977 HipSci___Whole_Exome_sequencing___Congenital_hyperinsulinia Other
2016-09-20
EGAS00001001978 HipSci___Whole_Exome_sequencing___Ataxia Other
2016-09-20
EGAS00001001979 HipSci___Whole_Exome_sequencing___HSP Other
2016-09-20
EGAS00001001980 HipSci___Whole_Exome_sequencing___Cardiomyopathy Other
2016-09-20
EGAS00001001981 HipSci___Whole_Exome_sequencing___Kabuki Other
2016-09-20
EGAS00001001982 HipSci___Whole_Exome_sequencing___Macular_dystrophy Other
2016-09-20
EGAS00001001983 HipSci___Whole_Exome_sequencing___PID Other
2016-09-20
EGAS00001001984 HipSci___Whole_Exome_sequencing___Retinitis_Pigmentosa Other
2016-09-20
EGAS00001001985 HipSci___Whole_Exome_sequencing___Usher syndrome and congenital eye defects Other
2016-09-20
EGAS00001001986 HipSci_RNASEQ_Alport Transcriptome Analysis
2016-09-20
EGAS00001001987 HipSci_RNASEQ_Battens Transcriptome Analysis
2016-09-20
EGAS00001001988 HipSci_RNASEQ_Congenital_hyperinsulinia Transcriptome Analysis
2016-09-20
EGAS00001001989 HipSci_RNASEQ_Kabuki Transcriptome Analysis
2016-09-20
EGAS00001001990 HipSci_RNASEQ_PID Transcriptome Analysis
2016-09-20
EGAS00001001991 HipSci_RNASEQ_Spastic_paraplegia Transcriptome Analysis
2016-09-20
EGAS00001001992 HipSci_RNASEQ_Ataxia Transcriptome Analysis
2016-09-20
EGAS00001001993 HipSci_RNASEQ_BPD Transcriptome Analysis
2016-09-20
EGAS00001001994 HipSci_RNASEQ_Hypertrophic_Cardiomyopathy Transcriptome Analysis
2016-09-20
EGAS00001001995 HipSci_RNASEQ_Macular_Dystrophy Transcriptome Analysis
2016-09-20
EGAS00001001996 HipSci_RNASEQ_Retinitis_Pigmentosa Transcriptome Analysis
2016-09-20
EGAS00001001997 HipSci_RNASEQ_Usher syndrome and congenital eye defects Other
2016-09-20
EGAS00001002005 HipSci HumanExome BeadChip analysis - Hereditary Cerebellar Ataxias Other
2016-09-23
EGAS00001002006 HipSci HumanExome BeadChip analysis - Hereditary Spastic Paraplegia Other
2016-09-23
EGAS00001002007 HipSci HumanExome BeadChip analysis - Kabuki syndrome Other
2016-09-23
EGAS00001002008 HipSci HumanExome BeadChip analysis - Usher syndrome and congenital eye defects Other
2016-09-23
EGAS00001002009 HipSci HumanExome BeadChip analysis - Alport Syndrome Other
2016-09-23
EGAS00001002010 HipSci HumanExome BeadChip analysis - Congenital Hyperinsulinia Other
2016-09-23
EGAS00001002011 HipSci HumanExome BeadChip analysis - Hypertrophic Cardiomyopathy Other
2016-09-23
EGAS00001002012 HipSci HumanExome BeadChip analysis - Primary immune deficiency Other
2016-09-23
EGAS00001002013 HipSci HumanExome BeadChip analysis - Bleeding and Platelet disorders Other
2016-09-23
EGAS00001002014 HipSci HumanExome BeadChip analysis - Macular Dystrophy Other
2016-09-23
EGAS00001002015 HipSci HumanExome BeadChip analysis - Retinitis Pigmentosa Other
2016-09-23
EGAS00001002016 HipSci HumanExome BeadChip analysis - Battens disease Other
2016-09-23
EGAS00001002020 HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Cerebellar Ataxias Other
2016-09-23
EGAS00001002021 HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Spastic Paraplegia Other
2016-09-23
EGAS00001002022 HipSci HumanHT 12 Expression BeadChip analysis - Kabuki syndrome Other
2016-09-23
EGAS00001002023 HipSci HumanHT 12 Expression BeadChip analysis - Usher syndrome and congenital eye defects Other
2016-09-23
EGAS00001002024 HipSci HumanHT 12 Expression BeadChip analysis - Alport syndrome Other
2016-09-23
EGAS00001002025 HipSci HumanHT 12 Expression BeadChip analysis - Congenital Hyperinsulinia Other
2016-09-23
EGAS00001002026 HipSci HumanHT 12 Expression BeadChip analysis - Hypertrophic Cardiomyopathy Other
2016-09-23
EGAS00001002027 HipSci HumanHT 12 Expression BeadChip analysis - Primary immune deficiency Other
2016-09-23
EGAS00001002028 HipSci HumanHT 12 Expression BeadChip analysis - Bleeding and Platelet disorders Other
2016-09-23
EGAS00001002029 HipSci HumanHT 12 Expression BeadChip analysis - Macular Dystrophy Other
2016-09-23
EGAS00001002030 HipSci HumanHT 12 Expression BeadChip analysis - Retinitis Pigmentosa Other
2016-09-23
EGAS00001002031 HipSci HumanHT 12 Expression BeadChip analysis - Battens disease Other
2016-09-23
EGAS00001002049 Prognostic relevance of microenvironmental factors CD163 and CD8 combined with EZH2 and chromosome 18 gain in a validation cohort of follicular lymphoma patients of the Lunenburg Lymphoma Biomarker Consortium Other
2016-09-27
EGAS00001002050 WES used for direct identification of clinically relevant neoepitopes presented on native human melanoma tissue by mass spectrometry Other
2016-09-27
EGAS00001002052 Genome-Wide Association Study of aspirin-induced PUD in a UK cohort Other
2016-09-29
EGAS00001002057 Characterization_of_genomic_landscape_of_Peripheral_T_cell_Lymphomas__not_otherwise_specified__PTCL_NOS_ Cancer Genomics
2016-09-30
EGAS00001002059 Exome_sequencing_of_a_cohort_of_Rett_syndromelike_patients Other
2016-10-03
EGAS00001002060 A_compendium_of_mutational_signatures_due_to_environmental_exposures Whole Genome Sequencing
2016-10-03
EGAS00001002064 Identification_of_genes_involved_in_congenital_disorders_of_glycosylation_and_3_methylglutaconic_aciduria Other
2016-10-03
EGAS00001002065 Similarity and diversity of the tumor microenvironment in multiple metastases: critical implications for overall and progression-free survival of high-grade serous ovarian cancer. Other
2016-10-03
EGAS00001002067 Whole_exome_sequencing_for_clarification_of_rare_causes_of_axonal_Charcot_Marie_Tooth_disease_ Other
2016-10-04
EGAS00001002068 Molecular_diagnosis_of_albinism Other
2016-10-04
EGAS00001002069 MYOSEQ project Other
2016-10-05
EGAS00001002070 BLUEPRINT Hematopoietic Stem/Progenitor Cell Methylomes Epigenetics
2016-10-06
EGAS00001002072 Single-cell RNA sequencing on 5063 single T cells isolated from peripheral blood, tumour and adjacent normal tissues from six hepatocellular carcinoma patients. Other
2016-10-07
EGAS00001002073 Combining transcription factor binding affinities with open chromatin data for accurate gene expression prediction Other
2016-10-10
EGAS00001002074 Gene_Characterization_in_Carbohydrate_metabolic_alterations__neonatel_diabetes___congenital_hyperinsulinemic__in_early_childhood Other
2016-10-10
EGAS00001002075 A mutation in VPS15 (PIK3R4) causes a ciliopathy and affects IFT20 release from the cis-Golgi Other
2016-10-10
EGAS00001002078 Reconstructing the dispersals and adaptive history of Bantu-speaking populations in Africa and North America Other
2016-10-12
EGAS00001002081 Sequencing_melanoma_germlines Other
2016-10-13
EGAS00001002082 T19_Chad_xten Whole Genome Sequencing
2016-10-14
EGAS00001002083 T19_Yemen Whole Genome Sequencing
2016-10-14
EGAS00001002084 Lebanon_LowCov_seq Whole Genome Sequencing
2016-10-14
EGAS00001002085 Lebanon_HighCov_seq Whole Genome Sequencing
2016-10-14
EGAS00001002091 A new subgroup of hepatocellular adenomas with sonic hedgehog pathway activation Other
2016-10-14
EGAS00001002092 The ICGC-TCGA DREAM Somatic Mutation Calling - Tumour Heterogeneity Challenge Other
2016-10-17
EGAS00001002093 Transcriptional and functional profiling defines human small intestinal macrophage subsets Other
2016-10-19
EGAS00001002094 Genomic and Epigenomic Features of Primary and Recurrent Hepatocellular Carcinomas Other
2016-10-19
EGAS00001002100 The Asian Diversity Project: genotyping of 37 Asian populations and ethnic groups Other
2016-10-22
EGAS00001002102 Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing Other
2016-10-24
EGAS00001002104 Psoriatic_arthritis Cancer Genomics
2016-10-25
EGAS00001002105 RNAseq data of polyA+ RNA from Leukocytes from 624 individuals of the SardiNIA cohort. Other
2016-10-26
EGAS00001002106 Detecting PKD1 variants in Polycystic Kidney Disease patients by single-molecule long-read sequencing Other
2016-10-28
EGAS00001002107 Melanoma_brain_metastases Cancer Genomics
2016-10-28
EGAS00001002108 De novo assembly of 150 Danish genomes reveals rich structural complexity Other
2016-10-31
EGAS00001002110 North American Brain Expression Consortium (NABEC) Exome Sequencing Other
2016-10-31
EGAS00001002111 Spatial genomic heterogeneity in multiple myeloma revealed by multi- region sequencing Other
2016-11-01
EGAS00001002113 Exome sequencing of United Kingdom Brain Expression Consortium samples Other
2016-11-02
EGAS00001002114 Patients with metastatic urothelial carcinoma Other
2016-11-02
EGAS00001002115 MYC Drives Progression of Small Cell Lung Cancer to a Variant Neuroendocrine Subtype with Vulnerability to Aurora Kinase Inhibition Other
2016-11-02
EGAS00001002117 Identification_of_synthetic_lethal_genes_by_CRISPR_Cas9_library Cancer Genomics
2016-11-08
EGAS00001002123 Meta-analysis of Genome-Wide-Association Sudies for plasma Factor XI Other
2016-11-09
EGAS00001002124 FFPE_normals_v2_gbm_wtsi_panel Cancer Genomics
2016-11-09
EGAS00001002128 Preclinical_evolution_of_haematological_malignancies_ Cancer Genomics
2016-11-09
EGAS00001002132 The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR Cancer Genomics
2016-11-09
EGAS00001002147 Genome-wide association study of prognosis in Crohn's disease Other
2016-11-11
EGAS00001002149 RNA-sequencing of six Pilocytic astrocytoma tumors Other
2016-11-14
EGAS00001002150 Inter and intra - tumor heterogeneity in Colorectal Cancer Other
2016-11-15
EGAS00001002153 The subclonal architecture of metastatic breast cancer: Results from a prospective community-based rapid autopsy program 'CASCADE' Other
2016-11-17
EGAS00001002154 SNU_PROSPECTIVE Other
2016-11-17
EGAS00001002156 Whole exome sequencing of Parkinson's disease patients from the United Kingdom Other
2016-11-18
EGAS00001002157 Resequencing_candidate_genes_for_male_spermatogenic_impairment Resequencing
2016-11-21
EGAS00001002158 A living biobank of breast cancer organoids captures disease heterogeneity Other
2016-11-21
EGAS00001002159 Assessment of de novo copy number variations in Italian patients with schizophrenia. Other
2016-11-21
EGAS00001002161 Methylation of Ewing sarcoma tumors (ICGC) Other
2016-11-22
EGAS00001002164 The Genetic Landscape of BCL2 Break Negative Follicular Lymphoma Other
2016-11-25
EGAS00001002165 Somatic_mutation_in_skin_epidermis__SMS_ Other
2016-11-25
EGAS00001002167 Osteosarcoma_X10 Cancer Genomics
2016-11-25
EGAS00001002168 Longitudinal analysis of treatment induced genomic alterations in gliomas Other
2016-11-26
EGAS00001002169 MeDALL epigenetics study Other
2016-11-28
EGAS00001002170 Scalable whole-genome single-cell library preparation without pre-amplification Other
2016-11-28
EGAS00001002171 Orphan_Tumour_Study___familial_neuroblastoma Other
2016-11-29
EGAS00001002173 Prebiotic inulin-type fructans induce specific changes in the human gut microbiota Other
2016-12-01
EGAS00001002174 The molecular landscape of colorectal cancer （17 cases） Other
2016-12-02
EGAS00001002175 Genomic and transcriptomic profiling of signalling networks in follicular lymphoma Other
2016-12-04
EGAS00001002176 The aim of this project is to identify, on 15 French Caucasian and 10 African-Caribbean men, through an integrative approach of DNA sequencing and transciptomic analyses, relevant genomic events that characterize or allow targeting the various phenotypes of aggressiveness of early stages of prostate cancer. Other
2016-12-05
EGAS00001002182 Genetic Basis of Hepatosplenic T Cell Lymphoma (HSTL) Other
2016-12-06
EGAS00001002183 Pediatric Non-Down Syndrome Acute Megakaryoblastic Leukemia is Characterized by Distinct Genomic Subsets with Varying Outcomes Other
2016-12-08
EGAS00001002184 miR-200-regulated CXCL12β promotes fibroblast heterogeneity and immunosuppression in ovarian cancers Other
2016-12-08
EGAS00001002185 Single-cell profiling maps the spectrum of crosstalk between glioma cells and tumor associated macrophages Other
2016-12-08
EGAS00001002186 Sequencing of pancreatic cancer primary tumors and metastases Other
2016-12-09
EGAS00001002189 Gene fusion and transcriptomic landscapes of sarcomas Other
2016-12-14
EGAS00001002190 Widespread DNA hypomethylation and differential gene expression in Turner syndrome Other
2016-12-14
EGAS00001002192 An Unusual Genomic Variant of Pancreatic Ductal Adenocarcinoma with an Indolent Clinical Course Other
2016-12-16
EGAS00001002193 Whole exome sequencing data for patients with Bosma arhinia microphthalmia syndrome (BAMS). Other
2016-12-19
EGAS00001002195 Transcriptional mechanisms of resistance to anti-PD-1 therapy Other
2016-12-20
EGAS00001002197 Oncogenic gene fusions in primary colon cancers Other
2016-12-21
EGAS00001002198 The genomic landscape of Burkitt Lymphoma Other
2016-12-22
EGAS00001002199 The genomic landscape of follicular and diffuse large B-cell lymphoma Other
2016-12-22
EGAS00001002200 Comprehensive analyses of somatic TP53 mutation in tumors with variable mutant allele frequency Other
2016-12-27
EGAS00001002201 THAP11 mutations in a patient with a cblX-like phenotype implicates THAP11 in the regulation of cobalamin metabolism and early vertebrate development Other
2016-12-31
EGAS00001002202 Genomic Landscape of Pediatric Myelodysplastic Syndromes Other
2017-01-03
EGAS00001002204 The_identification_of_genetic_vulnerabilities_in_head_and_neck_cancers_for_the_development_of_novel_therapies Cancer Genomics
2017-01-05
EGAS00001002205 Genomic data from analysis of the human placenta, part of the Pregnancy Outcome Prediction study (POPs) Other
2017-01-05
EGAS00001002206 Spectrum and significance of MYC and BCL2 mutations in DLBCL Other
2017-01-06
EGAS00001002207 Circumventing intratumoral heterogeneity to identify potential therapeutic targets in hepatocellular carcinoma. Details please contact lifuqiang@genomics and zhaoxin@genomics.cn. Other
2017-01-09
EGAS00001002210 Targeted_sequencing_of_blood_DNA_from_Human_twins_ Other
2017-01-09
EGAS00001002211 CancerLocator: Non-Invasive Cancer Diagnosis and Tissue-of-Origin Prediction Using Methylation Profiles of Cell-Free DNA Other
2017-01-09
EGAS00001002212 Whole-genome low pass sequencing of 3,514 Sardinian individuals Other
2017-01-10
EGAS00001002213 Same-day genomic and epigenomic diagnosis of brain tumors using realtime nanopore sequencing Other
2017-01-10
EGAS00001002216 Warm_autopsy__mutational_signatures_and_clonal_units Other
2017-01-11
EGAS00001002217 Clinical Cancer Genomic Profiling by Three-Platform Sequencing of Whole Genome, Whole Exome and Transcriptome Other
2017-01-11
EGAS00001002218 The Landscape of Genetic Alterations in Hepatocellular Carcinoma, 88 matched HCC tumour/normal pairs WGS belongs to ICGC LICA-CN project Other
2017-01-12
EGAS00001002221 Organoid_Derivation_Project__TGS Cancer Genomics
2017-01-12
EGAS00001002222 Organoid_Derivation_Project__WGS Cancer Genomics
2017-01-12
EGAS00001002223 Organoid_Derivation_Pilot__RNAseq Cancer Genomics
2017-01-12
EGAS00001002224 DONSON encodes a novel replication fork protection factor mutated in microcephalic dwarfism. Other
2017-01-12
EGAS00001002225 Tracing the origins of relapse in AML to stem cells Other
2017-01-12
EGAS00001002226 Aging and genome-wide patterns of DNA methylation in an African rainforest hunter-gathering population Other
2017-01-13
EGAS00001002228 Identification of fungal species in brain tissue from Alzheimer's disease Other
2017-01-16
EGAS00001002230 Whole genome bisulfite sequencing of hepatitis B virus-associated hepatocellular carcinoma tumor and non-cancerous samples Other
2017-01-17
EGAS00001002234 Global Anaplastic Thyroid Cancer Initiative Other
2017-01-17
EGAS00001002236 Genetics_of_gene_expression_in_human_macrophage_response_to_Salmonella Transcriptome Analysis
2017-01-18
EGAS00001002237 Sequencing of liver cancer cell lines Other
2017-01-19
EGAS00001002238 IBD_Whole_Genome_Sequencing Whole Genome Sequencing
2017-01-19
EGAS00001002239 Drug screening and whole genome sequencing of primary cells and cell lines from ovarian cancer patients to associate genomic aberrations with in vitro drug sensitivities Other
2017-01-20
EGAS00001002246 Indonesian sea-nomads genomic history Other
2017-01-26
EGAS00001002247 TRACERx 100: whole exome data of the first 100 TRACERx tumours Other
2017-01-30
EGAS00001002248 Genome-wide DNA methylation profiles by MeDIP-seq of cord blood cells and cord blood mononuclear cells obtained from twins conceived through in vitro fertilization and naturally conceived controls Other
2017-01-30
EGAS00001002249 Illumina Omni5 SNP chip genotyping of MacTel cases and unaffected controls for a genome-wide association study Other
2017-01-30
EGAS00001002251 This study explored and validated the clinical application of targeted NGS of circulating tumor DNA in identifying tumor-specific mutations and uncovering clinical actionable targets in a variety of solid tumors in large patient cohorts. Other
2017-01-30
EGAS00001002253 Genetic_vulnerability_of_knockout_cancer_lines Other
2017-01-31
EGAS00001002255 Functional_genomics_approaches_to_understand_osteoarthritis Transcriptome Analysis
2017-01-31
EGAS00001002256 A Functional Network of Gastric-Cancer-Associated Splicing Events Controlled by Dysregulated Splicing Factors Other
2017-02-01
EGAS00001002257 The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR_Custom Cancer Genomics
2017-02-01
EGAS00001002259 The_impact_of_the_human_leukaemia_virus_HTLV_1_on_host_gene_expression Whole Genome Sequencing
2017-02-02
EGAS00001002261 CELM Cancer Genomics
2017-02-02
EGAS00001002262 TSG_knock_out_in_hiPSCs Cancer Genomics
2017-02-02
EGAS00001002265 Regions of common inter-individual DNA methylation differences in human monocytes. Other
2017-02-03
EGAS00001002270 Genomic profiling of Acute Lymphoblastic Leukemia in Ataxia Telangiectasia patients reveals tight link between ATM mutations and chromothripsis Other
2017-02-07
EGAS00001002271 Integrative analysis of whole genome sequencing, RNA sequencing and methylome array of 20 carcinosarcomas. Other
2017-02-07
EGAS00001002272 A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family Other
2017-02-08
EGAS00001002273 Genetic_Heterogeneity_of_the_familial_gastric_neuroendocrine_tumors Other
2017-02-08
EGAS00001002274 WGS_of_AML_during_PARPi_therapy Cancer Genomics
2017-02-08
EGAS00001002275 Whole-genome Sequencing Suggests Mechanisms for 22q11.2 deletion-associated Parkinson’s disease Other
2017-02-08
EGAS00001002276 GWAS data (Illumina 2.5 M SNPs) in Cuban cohorts of dengue disease Other
2017-02-08
EGAS00001002278 Single_Cell_RNAseq_at_various_stages_of_HiPSCs_differentiating_toward_definitive_endoderm_and_endoderm_derived_lineages Transcriptome Analysis
2017-02-09
EGAS00001002294 Whole genome, whole exome, and targeted sequencing of high-grade meningioma tumor samples. Other
2017-02-11
EGAS00001002298 BGISEQ-500 Cancer Dataset - WGS tumour/normal pairs Other
2017-02-14
EGAS00001002299 Mesothelioma Genomics Study - WGS tumour/normal pairs Other
2017-02-14
EGAS00001002300 LICA-CN project - 116 liver cancer cases Other
2017-02-14
EGAS00001002301 Most HCCs in Taiwan show the mutational signature of aristolochic acid Other
2017-02-14
EGAS00001002305 The Ovarian Cancer Association Consortium OncoArray genome-wide association study Other
2017-02-14
EGAS00001002306 Whole-Genome Sequencing of a Healthy Aging Cohort. Other
2017-02-14
EGAS00001002309 Next_gen_seq_of_eye_cancers Cancer Genomics
2017-02-15
EGAS00001002312 Whole-exome sequencing of PTC, benign nodule and normal tissues in 28 patients Other
2017-02-16
EGAS00001002314 Sequencing of paediatric High Grade Gliomas and DIPG Other
2017-02-21
EGAS00001002317 18 Whole Exome Sequencing for Radiation Induced-Meningiomas Other
2017-02-21
EGAS00001002318 RNA seq on 19 samples of Radiation-Induced Meningiomas Other
2017-02-21
EGAS00001002319 Whole exome sequencing in RVOT patients Other
2017-02-22
EGAS00001002320 Massively parallel nanowell-based single-cell gene expression profiling Other
2017-02-22
EGAS00001002322 Functional_genomics_approaches_to_understand_osteoarthritis Population Genomics
2017-02-23
EGAS00001002323 The Immune Microenvironment, Genome–Wide Copy Number Aberrations and Survival in Mesothelioma Other
2017-02-23
EGAS00001002324 Genome-to-genome analysis highlights the impact of the human innate and adaptive immune systems on the hepatitis C virus Other
2017-02-24
EGAS00001002325 Kidney_Single_Cell_Study Transcriptome Analysis
2017-02-24
EGAS00001002326 Whole exome sequencing of an invasive diffuse intrinsic pontine glioma sampled from different sites Other
2017-02-27
EGAS00001002328 Genomic profiling of paediatric high grade gliomas from the HERBY clinical trial Other
2017-02-27
EGAS00001002329 Investigation_of_mutational_signatures_associated_with_DNMT3A_deficiency_ Cancer Genomics
2017-02-27
EGAS00001002331 160 WES and 25 WGS for HBV related HCC, and 15 WES for ICC belongs LICA-CN. Other
2017-03-01
EGAS00001002333 Mapping and phasing of structural variation in patient genomes using nanopore sequencing Other
2017-03-01
EGAS00001002334 A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus. Other
2017-03-01
EGAS00001002335 Drugging the catalytically inactive state of RET kinase in RET-rearranged tumors. Other
2017-03-02
EGAS00001002336 UK renal cancer samples genotyped on Illumina OmniExpress BeadChip Other
2017-03-02
EGAS00001002337 Poly(A) RNA sequencing of hepatocellular carcinoma tumors and their matched noncancerous liver tissues Other
2017-03-03
EGAS00001002338 whole genome sequence data of multifocal hepatocellular carcinoma Other
2017-03-03
EGAS00001002340 Somatic_mutation_and_clonal_evolution_in_premalignant_lung_disease Other
2017-03-06
EGAS00001002343 Copy number profiling of putative cancer stem from pleural effusion aspirates from breast cancer patients Other
2017-03-07
EGAS00001002344 Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome Other
2017-03-07
EGAS00001002346 Transcriptome sequencing of myelodysplasia Other
2017-03-09
EGAS00001002347 Edinburgh_Naevi_Cohort Cancer Genomics
2017-03-09
EGAS00001002352 In this study, we performed exon sequencing (WXS) of 80 paired Brain cancer tumors and adjacent normal tissues to identify novel potential biomarkers. We extracted mutational signatures which induce somatic mutations . Our study covers a comprehensive genetic framework that can be used in clinical trials and treatment modalities in Brain cancer. Other
2017-03-10
EGAS00001002364 Ongoing_mutagenesis_RNAseq Cancer Genomics
2017-03-10
EGAS00001002366 CEHM Cancer Genomics
2017-03-10
EGAS00001002368 HYPERMUTATION AND MALIGNANT PROGRESSION IN LOW-GRADE GLIOMA PATIENTS Other
2017-03-10
EGAS00001002372 Evolution_of_the_cancer_epigenome_in_myeloproliferative_neoplasms_2 Cancer Genomics
2017-03-13
EGAS00001002374 The molecular landscape of colorectal cancer （5 cases） Other
2017-03-14
EGAS00001002376 Molecular Subtype-specific Biomarkers Improves Colorectal Cancer Prognostication Other
2017-03-15
EGAS00001002377 Tumor-derived exosomes modulate PD-L1 expression in monocytes Other
2017-03-15
EGAS00001002379 Somatic_mutations_in_twin_breast_cancers Cancer Genomics
2017-03-15
EGAS00001002380 Botswana 15 autosomal unlinked microsatellites Other
2017-03-16
EGAS00001002382 Field_effect_of_healthy_and_diseased_livers Cancer Genomics
2017-03-16
EGAS00001002388 2017_AML_WGS Other
2017-03-21
EGAS00001002390 Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes Other
2017-03-21
EGAS00001002393 Genomic landscape of oral cancers (Complete Genomics WGS) Other
2017-03-22
EGAS00001002398 WGS of T-cell and NK-cell lymphoma for ICGC (NKTL-SG) Other
2017-03-27
EGAS00001002400 Biological insights from the whole genome sequences of human embryonic stem cell lines Other
2017-03-27
EGAS00001002402 Comprehensive investigation of genome architecture of papillary thyroid cancer with whole-exon sequencing in the Chinese population. Other
2017-03-28
EGAS00001002404 Comprehensive investigation of genome architecture of gastric adenocarcinoma with whole-genome sequencing in the Chinese population. Other
2017-03-29
EGAS00001002405 Targeted resequencing of ribosomal proteins in multiple myeloma patient samples. Other
2017-03-29
EGAS00001002406 Bisulfite-converted duplexes for the strand-specific detection and quantification of rare mutations Other
2017-03-29
EGAS00001002408 Whole Genome Sequencing of Liver Cancers Other
2017-03-30
EGAS00001002409 Human_primary_melanoma_project Other
2017-03-31
EGAS00001002410 Suppressors and activators of JAK-STAT signaling at diagnosis and relapse of acute lymphoblastic leukemia in Down Syndrome Other
2017-04-01
EGAS00001002413 Field_effect_of_healthy_and_diseased_livers_WGS Other
2017-04-04
EGAS00001002414 ChIP Seq data of multiple myeloma and plasma cell leukaemia cell lines Other
2017-04-04
EGAS00001002415 TRACERx 100: metastatic samples Other
2017-04-05
EGAS00001002416 WGS___Mutant_clone_mapping_in_normal_oesohagus_and_skin Cancer Genomics
2017-04-05
EGAS00001002418 Exome sequencing of pseudomyxoma peritonei Other
2017-04-07
EGAS00001002419 Clinical and genetic analysis of a rare syndrome associated with neoteny Other
2017-04-07
EGAS00001002420 Whole genome sequencing identified biomarker of response to PD1 blockade in Natural-killer/T-cell lymphoma Other
2017-04-10
EGAS00001002421 CD36 defines CML cells less sensitive to imatinib Other
2017-04-10
EGAS00001002422 The genomic landscape of germinal center derived B-cell lymphomas other than follicular, diffuse-large B-cell and Burkitt lymphom Other
2017-04-11
EGAS00001002423 Cisplatin increases sensitivity to FGFR inhibition in patient-derived xenograft models of lung squamous cell carcinoma Other
2017-04-11
EGAS00001002424 Cell fate mapping of human glioblastoma reveals an invariant stem cell hierarchy pre- and post-treatment Other
2017-04-11
EGAS00001002425 Whole Mitochondrial Sequencing of Gingivo-buccal Cancer: ICGC-India Project Other
2017-04-12
EGAS00001002428 A dataset compiled as a resource a for orthogonal assessment of exon CNV calling in NGS data Other
2017-04-18
EGAS00001002430 Deep single-cell RNA sequencing data for 12346 T cells from tumour, adjacent normal tissue and peripheral blood of treatment-naive NSCLC patients Other
2017-04-19
EGAS00001002431 Neurodegenerative_TGS Cancer Genomics
2017-04-20
EGAS00001002432 The evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusion Other
2017-04-21
EGAS00001002433 Genomic landscape of Chordoid Glioma Other
2017-04-24
EGAS00001002436 Subclonal evolution of four ER+ breast cancers determined by WGS and scRNA-Seq Other
2017-04-25
EGAS00001002437 Integrative genomic and transcriptomic analysis of adult leiomyosarcoma (HIPO-028, HIPO-018, HIPO-021) Other
2017-04-25
EGAS00001002438 Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells Transcriptome Analysis
2017-04-26
EGAS00001002439 Whole exome sequencing in patients with ALS and concomitant FTD lacking the C9orf72 repeat expansion Other
2017-04-26
EGAS00001002440 Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia Other
2017-04-26
EGAS00001002441 Successful immune checkpoint blockade in a patient with advanced stage microsatellite unstable biliary tract cancer (H021) Other
2017-04-26
EGAS00001002443 Transcriptional regulatory networks of tumor-associated macrophages that drive malignancy in mesenchymal glioblastoma Other
2017-05-02
EGAS00001002444 A combined circulating tumor DNA and protein biomarker-based liquid biopsy for the earlier detection of pancreatic cancer Other
2017-05-02
EGAS00001002445 Control samples, breast cancer clinical samples and matched patient-derived tumour xenografts (PDTXs) to develop and test a computational approach to discriminate human and mouse sequences in PDTXs Other
2017-05-03
EGAS00001002449 Integrative single-cell and cell-free plasma RNA transcriptomics elucidates placental cellular dynamics Other
2017-05-05
EGAS00001002450 Mutations in SPINK2 induce azoospermia Other
2017-05-05
EGAS00001002452 Whole_genome_sequencing_of_100_DDD_trios_with_suspected_noncoding_causal_mutations Whole Genome Sequencing
2017-05-08
EGAS00001002453 Comprehensive Molecular Analysis of Colon Cancer for the Identification and Validation of New Biomarkers Other
2017-05-09
EGAS00001002454 Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy Other
2017-05-09
EGAS00001002457 The demographic history and mutational load of African hunter-gatherers and farmers Other
2017-05-10
EGAS00001002460 SNP array data for the Milieu Intérieur cohort Other
2017-05-12
EGAS00001002461 Whole_Genome_Sequencing_of_INTERVAL Whole Genome Sequencing
2017-05-12
EGAS00001002462 PCR-free HiSeqX whole genome sequence data on 120 samples with triplet repeat expansions (premutation and full expansions) Other
2017-05-12
EGAS00001002463 ChIP-seq of GOF p53 mutants Other
2017-05-13
EGAS00001002471 Mutational_signatures_and_clonal_dynamics_in_normal_human_tissues Cancer Genomics
2017-05-16
EGAS00001002472 CINECA synthetic data.Please note: This study contains synthetic data (with cohort “participants” / ”subjects” marked with FAKE) has no identifiable data and cannot be used to make any inference about cohort data or results. Other
2017-05-16
EGAS00001002473 Fungal infection in neural tissue from Amyotrophic Lateral Sclerosis Other
2017-05-17
EGAS00001002474 Genomic_profiling_of_B_other_Adult_ALL_WGS Other
2017-05-17
EGAS00001002475 Identification of fusion transcripts by RNA-sequencing and Whole genome sequencing of a METABRIC patient sample Other
2017-05-18
EGAS00001002477 GENOMIC INSTABILITY IN MISMATCH REPAIR DEFICIENT COLORECTAL CANCER Other
2017-05-18
EGAS00001002478 Cell motility and migration as determinants of stem cell efficacy Other
2017-05-18
EGAS00001002479 Genome-wide DNA methylation profiles of NSCLC xenograft and primary lung tissues for the identification of epigenetic predictive biomarkers. Other
2017-05-22
EGAS00001002481 CNV detection in targeted NGS panel data Other
2017-05-23
EGAS00001002482 H3Africa - Genomic and Environmental Risk Factors for Cardiometabolic Disease in Africans Other
2017-05-24
EGAS00001002483 Hip OA Functional Genomics Transcriptome Analysis
2017-05-24
EGAS00001002484 RRBS sequencing of 7 tumour regions and a normal sample from a single TRACERx patient. Other
2017-05-25
EGAS00001002485 Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment Other
2017-05-26
EGAS00001002486 Kidney_tumour_DNA Cancer Genomics
2017-05-26
EGAS00001002487 Kidney_tumour_RNA Cancer Genomics
2017-05-26
EGAS00001002489 Paediatric IBD Mosaicism Other
2017-05-26
EGAS00001002490 Mutational signatures of aflatoxin Other
2017-05-29
EGAS00001002492 Genomic Profiling Reveals Spatial Intra-tumour Heterogeneity in Follicular Lymphoma Other
2017-05-31
EGAS00001002493 Whole_Exome_PC9_and_A375 Cancer Genomics
2017-06-01
EGAS00001002494 Profiling_molecular_heterogeneity_in_human_primary_microglia Transcriptome Analysis
2017-06-01
EGAS00001002495 Sampling of multi-centric lower grade glioma influences management and provides insight into gliomagenesis Other
2017-06-04
EGAS00001002496 H3K27ac ChIP-seq in TMPRSS2:ERG positive and negative prostate cancer tissue samples Other
2017-06-05
EGAS00001002499 Genetic Risk for Subsequent Neoplasms among Long-term Survivors of Childhood Cancer in the St. Jude Lifetime Cohort Other
2017-06-06
EGAS00001002501 Genome-wide expression profiles to compare array-based, RNAseq and NanoString technologies in patients with resected pancreatic ductal carcinoma. Other
2017-06-09
EGAS00001002504 Transcriptome sequencing of intravenous leiomyomatosis and uterine myoma Other
2017-06-09
EGAS00001002505 H3K27ac and RNA-seq data of neuroblastoma PDXs and/or primary tumors Other
2017-06-12
EGAS00001002506 Targeted next-generation sequencing detects novel gene-phenotype associations and expands the mutational spectrum in cardiomyopathie Other
2017-06-12
EGAS00001002507 ATRX mutant neuroblastoma is sensitive to EZH2 inhibition via modulation of neuronal differentiation. Other
2017-06-12
EGAS00001002508 Fibroblast heterogeneity and immunosuppressive environment in Human breast cancer Other
2017-06-13
EGAS00001002509 Combination Therapies for Personalised Cancer Medicine in drug resistant EGFR mutant lung cancer Other
2017-06-14
EGAS00001002511 Genomic and epigenomic characterization of juvenile myelomonocytic leukemia (JMML) Other
2017-06-14
EGAS00001002512 Mutation_burden_in_sun_exposed_eyelid__MSSE_ Other
2017-06-15
EGAS00001002515 Pharmacogenomic landscape of patient-derived cells informs precision oncology therapy Other
2017-06-16
EGAS00001002517 Distinct genomic profile and specific targeted drug responses in adult cerebellar glioblastoma Other
2017-06-19
EGAS00001002518 Linking the epigenetic landscape in chronic lymphocytic leukemia to deregulated chromatin networks Other
2017-06-20
EGAS00001002520 Local In Time Statistics for processual research Other
2017-06-21
EGAS00001002521 Cylindromas_sun_protected_and_exposed Cancer Genomics
2017-06-21
EGAS00001002523 Genome_Diversity_in_Africa_Project__Uganda Whole Genome Sequencing
2017-06-21
EGAS00001002526 The aim of this study was to identify underlying hub genes and dysregulated pathways associated with the development of HCC using bioinformatics analysis. Other
2017-06-21
EGAS00001002527 Establishing multiple omics baselines for three Southeast Asian populations in the Singapore Integrative Omics Study Other
2017-06-21
EGAS00001002528 Orthotopic Patient-Derived Xenografts of Pediatric Solid Tumors Other
2017-06-21
EGAS00001002533 Genome-wide genetic and epigenetic dataset of pancreatic acinar cell carcinomas Other
2017-06-23
EGAS00001002534 Orphan_Tumour_Study___RNAseq Cancer Genomics
2017-06-23
EGAS00001002535 Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Surname Population Genomics
2017-06-26
EGAS00001002536 A biobank of patient-derived pediatric brain tumor models Other
2017-06-27
EGAS00001002537 Integrative genomic analysis identifies multiple subtypes and therapeutic targets in acute erythroid leukemia Other
2017-06-27
EGAS00001002538 The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space Other
2017-06-27
EGAS00001002543 PanCuRx Translational Research Initiative Other
2017-06-28
EGAS00001002549 Genomic landscape of human diversity across Madagascar Other
2017-07-04
EGAS00001002551 Y_chromosome_mis_segregation_in_the_DLD_1_cell_line Cancer Genomics
2017-07-06
EGAS00001002553 Pilot_Fetal_Cell_Atlas_RNAseq Transcriptome Analysis
2017-07-07
EGAS00001002554 Genentech - Cell line exome sequencing Other
2017-07-07
EGAS00001002555 Plasma pQTLs in INTERVAL cohort Other
2017-07-10
EGAS00001002556 TGF-β attenuates tumour response to PD-L1 blockade by contributing to exclusion of T cells. Other
2017-07-10
EGAS00001002557 Copy-number signatures and mutational processes in ovarian carcinoma Other
2017-07-10
EGAS00001002558 Genomic diversity of the African-descent Makranis of Pakistan Other
2017-07-11
EGAS00001002559 Exome-wide somatic mutation characterization of small bowel adenocarcinoma Other
2017-07-11
EGAS00001002560 Single-cell RNA sequencing reveals cell-type specific eQTLs in peripheral blood mononuclear cells Other
2017-07-11
EGAS00001002562 Exome sequencing data from two myelosarcomas Other
2017-07-11
EGAS00001002565 Genetic history of the Comorian populations. Other
2017-07-12
EGAS00001002566 Combined clinical and gene expression score identifies high-risk individuals among follicular lymphoma patients on immunotherapy Other
2017-07-13
EGAS00001002567 Pilot study for Illumina TST170 NGS panel on cutaneous T cell lymphoma samples Other
2017-07-13
EGAS00001002568 KLB mutations in congenital hypogonadotropic hypogonadism Other
2017-07-13
EGAS00001002569 Genetic history of the Swahili population Other
2017-07-13
EGAS00001002570 Progression to AML is predictable and distinct from age related clonal hematopoiesis Other
2017-07-13
EGAS00001002571 Identification of cis-regulatory mutations generating de novo edges in personalized cancer gene regulatory networks Other
2017-07-17
EGAS00001002576 Comparative genomics research for Chinese colorectal cancer Other
2017-07-19
EGAS00001002577 Direct Detection of Early-stage Cancers Using Circulating Tumor DNA Other
2017-07-19
EGAS00001002578 Whole genome shotgun sequencing and somatic mutations data in Hepatocellular carcinoma Other
2017-07-20
EGAS00001002579 Combination Therapies for Personalised Cancer Medicine in 11-18 Other
2017-07-20
EGAS00001002581 Molecular profiling of MBD4-deficient acute myeloid leukaemia Other
2017-07-21
EGAS00001002582 Inhibiton of the GABPB1L-containing GABP tetramer is sufficient to reverse replicative immortality in TERT promoter mutant glioblastoma cells. Other
2017-07-21
EGAS00001002586 Transcriptome analysis in very preterm infants with chronic lung disease after birth Other
2017-07-24
EGAS00001002588 Systematic kinase inhibitor profiling identifies CDK9 as a synthetic lethal target in NUT midline carcinoma Other
2017-07-25
EGAS00001002589 High Grade Serous Ovarian Carcinomas Originate in the Fallopian Tube Other
2017-07-25
EGAS00001002591 Genes associated with pancreas development and function maintain open chromatin in iPSCs generated from human pancreatic beta cells Other
2017-07-25
EGAS00001002592 Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci Other
2017-07-25
EGAS00001002593 Illumina HiSeqX whole genome sequence data on 58 samples including 54 with known HTT triplet repeat expansions (2 premutation and 52 full expansions) Other
2017-07-25
EGAS00001002594 The exomic landscape of t(14,18) negative diffuse follicular lymphoma with 1p36 deletion Other
2017-07-26
EGAS00001002597 Whole Genomes Define Concordance in Matched Primary, Xenograft, and Organoid Models of Pancreas Cancer Other
2017-08-01
EGAS00001002598 Illumina HiSeqX and HiSeq 2000 whole genome sequence data on 3,001 ALS samples including 212 with known C9orf72 repeat expansions Other
2017-08-01
EGAS00001002599 Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells Epigenetics
2017-08-02
EGAS00001002602 H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis Other
2017-08-02
EGAS00001002604 Evolution and clinical impact of genetic epistasis within EGFR-mutant lung cancers Other
2017-08-03
EGAS00001002605 The chromatin accessibility signature of human immune aging stems from CD8+ T cells Other
2017-08-03
EGAS00001002606 Genetic and Functional Drivers of Diffuse Large B Cell Lymphoma Other
2017-08-03
EGAS00001002607 Comparative genomics research for Chinese colorectal cancer Other
2017-08-07
EGAS00001002608 MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma Cancer Genomics
2017-08-07
EGAS00001002609 Reduced Representation Bisulfite Sequencing (RRBS) in various tissues to discover DNA methylation markers for the diagnosis of breast and ovarian cancer. Other
2017-08-08
EGAS00001002610 Somatic_Variation_Angiosarcoma Cancer Genomics
2017-08-09
EGAS00001002612 The genomic landscape of cutaneous squamous cell carcinoma from immunosuppressed and immunocompetent patients reveals common drivers and a novel mutational signature associated with chronic azathioprine exposure Other
2017-08-09
EGAS00001002614 Capture Hi-C on MM Other
2017-08-11
EGAS00001002616 Breast cancer women lack normal lifelong immune response after full-term pregnancies Other
2017-08-14
EGAS00001002617 AngioPredict CNV and Exome data Other
2017-08-14
EGAS00001002618 Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH Epigenetics
2017-08-14
EGAS00001002619 Cryptic Relatedness in the Singapore Living Biobank Project Other
2017-08-15
EGAS00001002621 Multi-omics Profiling of Asian Breast Cancers Other
2017-08-16
EGAS00001002622 Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping Other
2017-08-16
EGAS00001002624 The_genetics_of_thinness_compared_to_obesity Population Genomics
2017-08-18
EGAS00001002625 Clonal evolution study of Intrahepatic cholangiocarcinoma in Zhongshan Hospital Other
2017-08-20
EGAS00001002626 Somatic_mutation_and_clonal_evolution_in_the_human_pancreas___WGS Cancer Genomics
2017-08-22
EGAS00001002627 Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance Other
2017-08-22
EGAS00001002628 2017_prospective_v2 Whole Exome Sequencing Other
2017-08-28
EGAS00001002630 Mutational spectrum of highly differentiated, fusion-negative rhabdomyosarcoma (set 1). Other
2017-08-28
EGAS00001002631 Performance comparison of three DNA extraction kits on human whole-exome data from formalin-fixed paraffin-embedded normal and tumor samples Other
2017-08-29
EGAS00001002632 Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome Other
2017-08-30
EGAS00001002633 _Isotype_resolved_sequencing_of_B_cell_receptor__in_sorted_memory_populations Transcriptome Analysis
2017-08-30
EGAS00001002634 Isotype_resolved_sequencing_of_B_cell_receptor__in_health_and_disease Transcriptome Analysis
2017-08-30
EGAS00001002635 Isotype_resolved_sequencing_of_B_cell_receptor_in_measles_virus_infection Transcriptome Analysis
2017-08-30
EGAS00001002636 Cross-tissue transcriptomic analysis of human secondary lymphoid organ residing ILC3 reveals a default quiescent state in the absence of inflammation Other
2017-08-30
EGAS00001002637 HDAC inhibitors in synovial sarcoma cells Other
2017-08-30
EGAS00001002639 The Southern African Human Genome Programme Other
2017-09-04
EGAS00001002641 Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population Other
2017-09-06
EGAS00001002642 Using_genetics_to_identify_cell_types_and_mechanisms_underlying_susceptibility_to_primary_sclerosing_cholangitis Transcriptome Analysis
2017-09-07
EGAS00001002643 Using_genetics_to_identify_cell_types_and_mechanisms_underlying_susceptibility_to_primary_sclerosing_cholangitis Population Genomics
2017-09-07
EGAS00001002645 Genome-wide search for higher order epistasis as modifiers of treatment effects on bone mineral density in childhood cancer survivors Other
2017-09-08
EGAS00001002646 Identification of a Fumarate-Hydratase Deficient-like RCC Subtype with Convergent Pathway Alterations Other
2017-09-08
EGAS00001002649 Transcriptional_analysis_of_cells_from_lungs Cancer Genomics
2017-09-11
EGAS00001002650 Ultra-fast multiplex small DNA sequencing on the MinION nanopore sequencing platform Other
2017-09-12
EGAS00001002652 Childhood_arthritis_DNA Cancer Genomics
2017-09-13
EGAS00001002654 A system-wide approach to monitor responses to synergistic BRAF and EGFR inhibition in colorectal cancer cells Other
2017-09-13
EGAS00001002655 DEEP IHEC release 2017 Other
2017-09-13
EGAS00001002656 H3Africa - Collaborative African Genomics Network Other
2017-09-14
EGAS00001002657 Detection of clinically relevant genetic and transcriptomic landscape in DLBCL uniformly treated by R-CHOP Other
2017-09-15
EGAS00001002658 Somatic_mutation_and_clonal_evolution_in_the_human_bladder_WGS Cancer Genomics
2017-09-15
EGAS00001002659 Somatic_mutation_and_clonal_evolution_in_the_human_bladder_TGS Cancer Genomics
2017-09-15
EGAS00001002660 RNA sequencing data of 66 matched primary and recurrent high grade serous ovarian cancer Other
2017-09-15
EGAS00001002662 Multisample genomic analysis of solid childhood cancers using high resolution SNP-arrays, Whole Exome Sequencing and Targeted Deep Sequencing. Other
2017-09-18
EGAS00001002664 Exome_trios_in_patients_with_gastroschisis Other
2017-09-19
EGAS00001002665 Family-based GWAS for CRSwNP Other
2017-09-19
EGAS00001002667 Immunodeficiency_ Other
2017-09-20
EGAS00001002668 WGS of 32 paired SRCC samples Other
2017-09-22
EGAS00001002670 We performed whole-exome sequencing of 20 samples (10 actinic keratosis and 10 cutaneous squamous cell carcinoma) to investigate a potential relationship between DNA methylation-based subtypes and genetic mutation patterns (Rodriguez-Paredes et al., Nat Commun 2017) Other
2017-09-26
EGAS00001002671 MicroRNA expression in malignant and benign breast tissue – the Norwegian Women and Cancer study Other
2017-09-26
EGAS00001002674 Y_phylogeny_haplogroupDE Resequencing
2017-09-28
EGAS00001002676 Liver biopsy derived induced pluripotent stem cells provide an unlimited supply for the generation of patient-specific hepatocyte-like cells Other
2017-09-28
EGAS00001002678 Genome-wide analysis of genetic risk factors for rheumatic heart disease in Aboriginal Australians provides support for pathogenic molecular mimicry Other
2017-09-29
EGAS00001002679 Employing_single_cell_sequencing_for_detection_of_mutational_signatures_reflecting_on_going_mutagenesis_ Cancer Genomics
2017-09-29
EGAS00001002680 WGS___Exploration_of__mutational_processes_in_human_cancer_cell_lines Cancer Genomics
2017-09-29
EGAS00001002681 Genome-wide mutational consequences of nucleotide excision repair-deficiency through XPC deletion in a human adult stem cell culture Other
2017-10-02
EGAS00001002682 The identification of genetic vulnerabilities in head and neck cancers for the development of novel treatments. Other
2017-10-03
EGAS00001002684 Characterization of genetic intratumor heterogeneity in colorectal cancer and matching patient-derived spheroid cultures. Other
2017-10-04
EGAS00001002685 WGS of breast cancer diagnosed during pregnancy and matched control Other
2017-10-05
EGAS00001002687 Differential Presence of Exons in Cell-Free DNA Reveals Different Patterns in Colorectal Cancer Between Metastatic and Non-Metastatic Patients Other
2017-10-06
EGAS00001002692 Wilms_Tumour_organoid_sequencing_WGS Cancer Genomics
2017-10-06
EGAS00001002694 MMR (DNA mismatch repair) pathway in human samples Other
2017-10-06
EGAS00001002696 Therapeutic Targeting of Ependymoma as Informed by Oncogenic Enhancer Profiling Other
2017-10-10
EGAS00001002697 Alternative splicing isoforms in patient-derived hepatocellular carcinoma cells Other
2017-10-11
EGAS00001002698 Gut microbiome modulates response to anti PD1 immunotherapy in metastatic melanoma patients Other
2017-10-11
EGAS00001002699 TCR β-chain repertoire characterization of regulatory and conventional T cells in peripheral blood from breast cancer patients and healthy individuals. Other
2017-10-12
EGAS00001002700 Genome-wide DNA Methylation is Predictive of Outcome in Juvenile Myelomonocytic Leukemia Other
2017-10-13
EGAS00001002702 Multi-omics data of 1000 Inflammatory Bowel Disease patients Other
2017-10-23
EGAS00001002703 The integrated genomic and immune landscapes of lethal metastatic breast cancer. Other
2017-10-23
EGAS00001002704 Dynamics of neoantigen landscape during immunotherapy Other
2017-10-23
EGAS00001002705 Whole exome sequencing of cell-free DNA reveals temporo-spatial heterogeneity and identifies treatment-resistant clones in neuroblastoma Other
2017-10-25
EGAS00001002707 Sequencing-based counting and size profiling of plasma Epstein-Barr virus DNA enhance population screening of nasopharyngeal carcinoma. Other
2017-10-27
EGAS00001002708 Targeted_sequencing_of_cylindroma_patients Other
2017-10-27
EGAS00001002709 Comprehensive genomic profiling of matched glioblastoma tumours, cell-lines, and xenografts reveals genomic stability and adaptation to disparate growth environments Other
2017-10-28
EGAS00001002714 Keratinocyte_CRISPR_screens Cancer Genomics
2017-11-02
EGAS00001002717 Defining the metastasome in colorectal cancer: Implications for hypotheses on metastasis evolution and personalized therapy (HIPO-032) Other
2017-11-03
EGAS00001002718 We performed whole-exome sequencing and whole epigenome sequencing (RRBS) of samples collected from different time points during radiotherapy from thirty-four ESCC patients. We compared the genetic and epigenetic features of the different time biopsy samples to reveal the changes in ESCC received radiotherapy. Other
2017-11-06
EGAS00001002719 We performed whole-exome sequencing and whole epigenome sequencing (RRBS) of samples collected from different time points during radiotherapy from thirty-four ESCC patients. We compared the genetic and epigenetic features of the different time biopsy samples to reveal the changes in ESCC received radiotherapy. Other
2017-11-06
EGAS00001002720 Defective Homologous Recombination DNA Repair as Therapeutic Target in Advanced-Stage Chordoma (HIPO_021) Other
2017-11-06
EGAS00001002721 Characterization of a human iPSC-derived islet differentiation model Other
2017-11-06
EGAS00001002723 Genetic_Overlap_between_Metabolic_and_Psychiatric_disease Whole Genome Sequencing
2017-11-09
EGAS00001002724 Angiopredict: predicting response for bevacizumab treatment Other
2017-11-09
EGAS00001002725 MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_squamous_cell_carcinoma Cancer Genomics
2017-11-09
EGAS00001002726 MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__pancreas Cancer Genomics
2017-11-09
EGAS00001002727 Exome and RNA sequencing of Greenlanders Other
2017-11-13
EGAS00001002728 CancerDetector: Ultrasensitive and Non-Invasive Cancer Detection at the Resolution of Individual Reads using Cell-free DNA Methylation Sequencing Data Other
2017-11-15
EGAS00001002729 We describe a method to culture organoids from adult human kidney tissue and describe applications for the culture system. Other
2017-11-16
EGAS00001002730 Brain transcriptome of hereditary cerebral haemorrhage with amyloidosis–Dutch type (HCHWA-D) Other
2017-11-16
EGAS00001002731 Himalayan_population_genetic_study Population Genomics
2017-11-16
EGAS00001002733 Targeted next-generation sequencing of 13 chordoid gliomas of the third ventricle Cancer Genomics
2017-11-22
EGAS00001002736 Molecular characterization of endothelial cells under conditions associated with hematopoietic niche formation in humans Other
2017-11-22
EGAS00001002737 Evolutionary analysis of primary tumors and metastatic lesions from 20 breast cancer patients (99 samples in total) using exome sequencing data. Other
2017-11-23
EGAS00001002738 X chromosomal genetic variants are associated with childhood obesity Other
2017-11-26
EGAS00001002740 Targeted Gene Panel for 171 PTCLs Other
2017-11-27
EGAS00001002742 The_British_Autozygosity_Populations_BioResource Other
2017-11-28
EGAS00001002743 Aggressive genomic features in clinicallyindolent primary HHV8-negative effusion-based lymphoma Other
2017-11-29
EGAS00001002744 The molecular basis of T-PLL is an actionable perturbation of TCL1/ATM- and epigenetically instructed damage responses Other
2017-11-29
EGAS00001002745 Next-Generation Sequencing of AV Nodal Reentry Tachycardia patients Other
2017-11-30
EGAS00001002746 BAMSE (Swedish abbreviation for Children, Allergy, Milieu, Stockholm, Epidemiology) Other
2017-11-30
EGAS00001002747 Somatic_mutation_and_clonal_evolution_in_premalignant_lung_disease___WGS Cancer Genomics
2017-12-01
EGAS00001002749 Chromatin_accessability_in_cytokine_induced_immune_cell_states Epigenetics
2017-12-04
EGAS00001002750 Mitochondrial DNA mutations contribute to autism and also to the characteristics of mitochondrial disorders present in patients with autism spectrum disorders Other
2017-12-04
EGAS00001002751 Antisense long non-coding RNAs are deregulated in skin tissue of patients with systemic sclerosis Other
2017-12-04
EGAS00001002753 Defective T-cell expansion in RASGRP1 deficiency Other
2017-12-04
EGAS00001002754 IBD_Whole_Genome_Sequencing Whole Genome Sequencing
2017-12-07
EGAS00001002755 The European Bank for Induced Pluripotent stem cells (EBiSC) is designed to address the increasing demand by iPSC researchers for quality-controlled, disease-relevant research grade iPSC lines, data and cell services.In this study Whole Genome Sequencing was performed on a selection of lines from the project. Other
2017-12-14
EGAS00001002756 GWAS in a dengue Thai cohort Other
2017-12-14
EGAS00001002757 Aberrant ERBB4-SRC Signaling as a Hallmark of Group 4 Medulloblastoma Revealed by Integrative Phosphoproteomic Profiling Other
2017-12-14
EGAS00001002758 Colorectal adenomas and carcinomas NKI-AvL TGO series Gut2009 Other
2017-12-14
EGAS00001002759 NRG1 Fusions in KRAS Wild-type Pancreatic Cancer (H021) Other
2017-12-15
EGAS00001002760 Germline alterations of acute myeloid leukemia Other
2017-12-15
EGAS00001002761 Comprehensive genetic analysis of uveal melanoma heterogeneity during metastatic progression Other
2017-12-15
EGAS00001002762 HSC_population_dynamics_KSP_samples Cancer Genomics
2017-12-15
EGAS00001002763 Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer Other
2017-12-15
EGAS00001002764 Detection and localization of surgically resectable cancers with a multi-analyte blood test Other
2017-12-16
EGAS00001002765 Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T-cell lymphomas with hemophagocytic lymphohistiocytic syndrome Other
2017-12-18
EGAS00001002766 Co-infection of fungi and bacteria in brain tissue of Alzheimer’s patients. Other
2017-12-18
EGAS00001002767 The genomic and radiomic complexity of multifocal prostate cancer Other
2017-12-18
EGAS00001002769 Insular Celtic population structure and genomic footprints of migration Other
2017-12-18
EGAS00001002770 DSRCT RNA genomic sequencing Other
2017-12-18
EGAS00001002771 Mutational spectrum of highly differentiated, fusion-negative rhabdomyosarcoma (set 2). Other
2017-12-19
EGAS00001002772 An integrated molecular study of 20 hepatoblastoma pairs using whole genome sequencing and RNA sequencing Other
2017-12-20
EGAS00001002773 Mutational profiling of LUAD in young never-smokers Other
2017-12-20
EGAS00001002777 Phylogenetic analysis of treatment-naive metastases using whole exome and genome sequencing data Other
2017-12-21
EGAS00001002778 Evolutionary analysis of pancreatic cancer and coexistent precursor lesions using whole exome sequencing data Other
2017-12-21
EGAS00001002782 Kibbutzim Family study Other
2017-12-28
EGAS00001002783 Whole-exome sequencing reveals the origin and evolution of Hepato-Cholangiocarcinoma Other
2018-01-01
EGAS00001002784 Patient-derived organoids model treatment response of metastatic gastrointestinal cancers (targeted and whole-genome sequencing) Other
2018-01-02
EGAS00001002786 An Empirical Approach Leveraging Tumorgrafts to Dissect the Tumor Microenvironment in Renal Cell Carcinoma Identifies Missing Link to Prognostic Inflammatory Factors Other
2018-01-04
EGAS00001002787 Whole_Genome_Sequencing_of_INTERVAL Other
2018-01-05
EGAS00001002788 Genomic analysis Nasopharyngeal cancer through whole exome sequencing and whole genomic sequencing. Other
2018-01-08
EGAS00001002789 CD49f single-cell methylomes Other
2018-01-09
EGAS00001002790 Preferential infiltration of distinct Vγ9δ2 T cells into Glioblastoma multiforme Other
2018-01-10
EGAS00001002791 Deep single-cell RNA sequencing data for 11138 T cells from tumour, adjacent normal tissue and peripheral blood of treatment-naive CRC patients. The DATA ACCESS AGREEMENT is provided at https://github.com/zhangyybio/single-T-cell-data-access. Applicants can request access to the data by directly downloading it or by sending an email to cancerpku@pku.edu.cn. The process that is used to approve an application includes verifying the institution, participants and research purposes of the application. In general this process will take about two weeks. In principal, any scientific research program complying with the laws and bioethic regulation policies of China will be approved. Other
2018-01-10
EGAS00001002792 Breast cancer DNA repair Other
2018-01-10
EGAS00001002793 TRACERx Renal 100 Other
2018-01-10
EGAS00001002795 Molecular profiling of acinar cell carcinoma of the salivary glands Other
2018-01-11
EGAS00001002796 Somatic IL4R Hotspot Mutations in Primary Mediastinal Large B-cell lymphoma lead to constitutive JAK-STAT activation Other
2018-01-11
EGAS00001002797 DNA hypermethylation and differential gene expression associated with Klinefelter syndrome Other
2018-01-12
EGAS00001002798 Hominin-specific NOTCH2 paralogs expand human cortical neurogenesis through regulation of Delta/Notch interactions. Other
2018-01-15
EGAS00001002801 Analysis of Complex Genomic Rearrangements of Lung Adenocarcinomas Other
2018-01-16
EGAS00001002802 RNA-seq profiling of NKX6.1 reporter iPSC lines for isolation and analysis of functionally relevant neuronal and pancreas populations Other
2018-01-16
EGAS00001002803 Sensitive and Frequent Identification of High Avidity Neo-epitope Specific CD8 + T-cells in Immunotherapy-naïve Ovarian Cancer Other
2018-01-18
EGAS00001002804 2018_ETO_WGS Other
2018-01-19
EGAS00001002805 Predictor_RIO_TNBC Cancer Genomics
2018-01-19
EGAS00001002806 Predictor_ChemoNEAR_TNBC Cancer Genomics
2018-01-19
EGAS00001002807 Genomic profiling of matched well differentiated and de-differentiated liposarcoma. Other
2018-01-19
EGAS00001002809 Inherited genetic predisposition to childhood acute lymphoblastic leukemia investigated using a genome wide association study. Other
2018-01-23
EGAS00001002811 Whole-Exome Sequencing of Salivary Gland Mucoepidermoid Carcinoma Other
2018-01-23
EGAS00001002812 Whole-Genome Sequencing of Salivary Gland Adenoid Cystic Carcinoma Other
2018-01-23
EGAS00001002814 Natural variation of circulating RNAs in human serum Other
2018-01-24
EGAS00001002816 Prostate Cancer and Normal Adjacent Prostate RNA-seq samples, NGS-ProToCol Other
2018-01-25
EGAS00001002818 Whole-exome ultra-high throughput sequencing in brain samples of suicide victims who had suffered from major depressive disorder and control subjects who had died from other causes Other
2018-01-26
EGAS00001002819 2014_AML_WES_51 samples Other
2018-01-26
EGAS00001002820 Molecular subtypes of malignant peritoneal mesothelioma Other
2018-01-27
EGAS00001002822 Psoriatic_arthritis_WGS Cancer Genomics
2018-01-29
EGAS00001002823 Physiological and genetic adaptations to diving in Sea Nomads Other
2018-01-29
EGAS00001002825 Whole genome and whole exome sequencing of epilaptic patients Other
2018-01-29
EGAS00001002826 A novel subset of human CD33+ haematopoietic stem cells characterized at single-cell resolution Other
2018-01-31
EGAS00001002827 Ibrutinib induces a global chromatin reorganisation in chronic lymphocytic leukaemia Other
2018-01-31
EGAS00001002830 Single cell sequencing reveals the origin and the order of mutation acquisition in T-cell acute lymphoblastic leukemia. Other
2018-02-05
EGAS00001002831 Size-tagged preferred ends in maternal plasma DNAshed light on the production mechanism and showutility in noninvasive prenatal testing Other
2018-02-06
EGAS00001002832 Transcriptome profiling of human plucked frontal and occipital hair follicles Other
2018-02-06
EGAS00001002833 Genomic profiling of ovarian adult type granulosa cell tumors Other
2018-02-06
EGAS00001002836 DNA methylation using EPIC array in UK population study Other
2018-02-07
EGAS00001002839 The interface of malignant and immunologic clonal dynamics in high-grade serous ovarian cancer Other
2018-02-07
EGAS00001002840 A novel breast cancer cell line derived from a metastatic bone lesion of a breast cancer patient Other
2018-02-08
EGAS00001002842 Somatic_mutation_and_clonal_evolution_in_the_human_bladder_WES Cancer Genomics
2018-02-08
EGAS00001002843 Korean Lung Cancer - 36 pair WES data Other
2018-02-09
EGAS00001002844 2014_Lung_sq_WES Other
2018-02-09
EGAS00001002845 Single cell sequencing of breast cancer T cells reveals a tissue-resident memory subset associated with improved prognosis RNASeq
2018-02-12
EGAS00001002846 Whole exome sequencing of longitudinal samples from a melanoma patient receiving MEK plus CDK4/6 inhibitor therapy. Other
2018-02-12
EGAS00001002847 ALPI deficiency and inflammatory bowel disease Other
2018-02-13
EGAS00001002850 A genomic approach towards an understanding of clonal evolution and disease progression in multiple myeloma Other
2018-02-16
EGAS00001002851 Transcriptome sequencing of Gingivo-buccal Cancer : ICGC-India Project_YR03 Other
2018-02-16
EGAS00001002852 Whole Exome sequencing of Gingivo-buccal Cancer : ICGC-India Project_Batch04 Other
2018-02-16
EGAS00001002853 Genomic and functional fidelity of small cell lung cancer patient-derived xenografts Other
2018-02-16
EGAS00001002854 Colorectal adenomas, carcinomas and adjacent normal NKI-AvL TGO series NGS-ProToCol Other
2018-02-16
EGAS00001002856 Integrated analysis of relapsed B-cell precursor Acute Lymphoblastic Leukemia identifies subtype-specific cytokine and metabolic signatures Other
2018-02-16
EGAS00001002857 Somatic_mutation_and_clonal_evolution_normal_breast_tissue_WGS Other
2018-02-16
EGAS00001002858 Somatic_mutation_and_clonal_evolution_normal_breast_tissue_TGS Cancer Genomics
2018-02-16
EGAS00001002859 Targeted panel data for newly diagnosed myeloma patients. Other
2018-02-16
EGAS00001002860 Whole-genome and transcriptome sequencing of tumor-stage mycosis fungoides Other
2018-02-19
EGAS00001002861 Investigating_the_impact_of_MBD4_on_the_mutability_of_the_germline Whole Genome Sequencing
2018-02-20
EGAS00001002863 Small_molecule_inhibitors_in_melanoma___Kenski___Kong___WES Cancer Genomics
2018-02-20
EGAS00001002864 Genome analysis of oesophageal cancer and Barrett's oesophagus Other
2018-02-20
EGAS00001002865 Human Pancreatic Beta Cell lncRNAs Control Cell-Specific Regulatory Networks Other
2018-02-21
EGAS00001002866 Exploring_the_heterogeneity_of_sarcoma_using_single_cell_sequencing_ Cancer Genomics
2018-02-21
EGAS00001002869 Exome and RNA sequencing data from 32 ocular and extraocular sebaceous carcinomas Other
2018-02-21
EGAS00001002871 Targeted exome sequencing of pleomorphic invasive lobular carcinoma (PILC). Other
2018-02-22
EGAS00001002872 Whole genome analysis of mutation hotspots in gastric cancer Other
2018-02-23
EGAS00001002873 Clonal_haematopoiesis_in_patients_with_AAA Cancer Genomics
2018-02-23
EGAS00001002874 Foundation Medicine Genomic Data Used to Identify Prognostic Markers and Fusion Genes in Multiple Myeloma Other
2018-02-23
EGAS00001002875 This project aims to study human memory capacity, including short-term memory and long-term memory, systematically via genome-wide association studies Other
2018-02-24
EGAS00001002876 PanProstate Cancer Group UK data Other
2018-02-27
EGAS00001002877 Transcriptional and DNA binding profiling of CEBPE in REH acute lymphoblastic leukaemia cells using shRNA RNA-Seq and ChIP-Seq Other
2018-02-27
EGAS00001002879 RNA-seq of Liver Cancer Other
2018-02-28
EGAS00001002882 scRNA-seq data of human nuclei collected from the temporal cortex of 17 individuals. Other
2018-03-01
EGAS00001002884 Genomic analysis of Japanese gastric cancer (345 gastric cancers of NCC) Other
2018-03-02
EGAS00001002885 Profiling_heterogeneity_in_Human_derived_IPSC_neurons Transcriptome Analysis
2018-03-02
EGAS00001002886 A whole genome analysis of single fetal human stem cells from the liver and the intestine Other
2018-03-02
EGAS00001002888 Whole Genome Sequencing of HCC Other
2018-03-02
EGAS00001002889 Integrated genetic and epigenetic analysis of myxofibrosarcoma Other
2018-03-02
EGAS00001002891 Exome sequencing of 142 gastric cancer and matched normal from Japanese cohorts (UT) Other
2018-03-02
EGAS00001002892 Exome sequencing of 102 gastric cancer and matched normal from Japanese cohorts (YCU) Other
2018-03-02
EGAS00001002893 Exome sequencing demonstrates a dual origin of relapses in retinoic-acid resistant acute promyelocytic leukemia. Other
2018-03-05
EGAS00001002894 The light chain IgLV3-21 defines a new poor prognostic subgroup in Chronic Lymphocytic Leukemia: results from a multicenter study Other
2018-03-06
EGAS00001002895 Using human induced pluripotent stem cells (iPSC) and iPSC-derived neurons to explore cellular phenotypes associated with schizophrenia. Other
2018-03-06
EGAS00001002896 Somatic_mutation_profiling_of_intestinal_crypts_from_IBD Whole Genome Sequencing
2018-03-07
EGAS00001002897 2015_AML_ETO Other
2018-03-08
EGAS00001002898 2015_AML_ETO_WGS_additional Other
2018-03-08
EGAS00001002899 Whole genome characterisation of lung cancer organoids and tissue Other
2018-03-08
EGAS00001002901 Hypothalamic transcriptome in Prader-Willi syndrome Other
2018-03-08
EGAS00001002903 PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice Other
2018-03-09
EGAS00001002907 HG_Retroduplications_in_Neurodevelopmental_Disorders Whole Genome Sequencing
2018-03-13
EGAS00001002908 Dynamics of multiple resistance mechanisms in plasma DNA and their clinical implications for NSCLC patients receiving EGFR-targeted therapies Other
2018-03-13
EGAS00001002910 Molecular analysis of giant cell lesions Other
2018-03-13
EGAS00001002911 Exploiting immune cell receptor information to quantify index switching in single cell transcriptome sequencing experiment Other
2018-03-14
EGAS00001002915 Japan PBC-GWAS Haplotype Study Other
2018-03-14
EGAS00001002917 Human islet 3D chromatin maps provide insights into type 2 diabetes Other
2018-03-19
EGAS00001002919 Genomic Heterogeneity and the Small Renal Mass Other
2018-03-20
EGAS00001002920 SS18-SSX-mediated hijacking of BAF complexes drives synovial sarcoma Other
2018-03-20
EGAS00001002921 Genome Asia 100K Project Other
2018-03-20
EGAS00001002922 Leeds Melanoma Cohort (LMC) gene expression study Other
2018-03-21
EGAS00001002923 Molecular evolution and clinical trajectories of prostate cancer identifies novel markers for risk stratification Other
2018-03-22
EGAS00001002926 502 present-day genotypes included in the '137 ancient human genomes from across the Eurasian steppe' publication Other
2018-03-23
EGAS00001002927 RNA-seq analysis of human skin Other
2018-03-23
EGAS00001002928 Clinical activity and molecular correlates of response to atezolizumab alone or in combination with bevacizumab versus sunitinib in renal cell carcinoma Other
2018-03-23
EGAS00001002929 Human_Developmental_Cell_Atlas_HDCA___WGS Cancer Genomics
2018-03-26
EGAS00001002931 Benchmarking_CRISPR_Whole_genome_Drop_out_Screen___B_S Cancer Genomics
2018-03-26
EGAS00001002932 RNAseq of 76 samples from Uveal Melanoma tumors Other
2018-03-26
EGAS00001002933 Single-cell transcriptome sequencing of regulatory and conventional T cells in breast cancer patients and healthy individuals. Other
2018-03-27
EGAS00001002935 Infant_Spindle_Tumour_Study Cancer Genomics
2018-03-27
EGAS00001002936 Genome-wide discovery of somatic coding and regulatory variants in Diffuse Large B-cell Lymphoma Other
2018-03-27
EGAS00001002937 GoDARTS T2D-GENES Exome Sequencing Study is a subset of the ~52,000 Type 2 diabetes exome sequencing project. Other
2018-03-27
EGAS00001002938 Gastric_Mutational_Signatures__GMS_ Cancer Genomics
2018-03-28
EGAS00001002939 Gastric_Mutational_Signatures__GMS_ Cancer Genomics
2018-03-28
EGAS00001002940 Germline DNMT3A mutation in mother-son pair with AML Other
2018-03-30
EGAS00001002941 The genomic landscape of lung adenocarcinoma in East Asians Other
2018-04-03
EGAS00001002945 RNA Sequencing of Colorectal Liver Metastases Other
2018-04-04
EGAS00001002947 The spatio-temporal evolution of lymph node spread in early breast cancer Other
2018-04-05
EGAS00001002948 Lymphoctye_colony_WGS Cancer Genomics
2018-04-05
EGAS00001002951 503 genotypes from Inner Asia used in 'Close inbreeding and low genetic diversity in Inner Asian human populations despite geographical exogamy' publication Other
2018-04-05
EGAS00001002952 Colorectal advanced adenomas NKI-AvL TGO COCOS series Other
2018-04-06
EGAS00001002953 Colorectal adenomas, NKI-AvL TGO series Stool-Proteomics Other
2018-04-06
EGAS00001002954 Whole-genome sequencing reveals genomic signatures associated with the inflammatory microenvironments in Chinese NSCLC patients Other
2018-04-09
EGAS00001002955 To determine the mutational impact of the in vitro culture, clonal human adult and pluripotent stem cell lines were subjected to a second clonal step after 3 months of culture. These subclones were whole genome sequenced to identify all the mutations that accumulated during the 3 month culture period. Other
2018-04-10
EGAS00001002957 Multiple esclerosis and mixed microbial infections Other
2018-04-11
EGAS00001002962 WES_of_adult_intellectual_disabilities_with_co_morbid_psychiatric_disorders Other
2018-04-17
EGAS00001002963 Inference_of_B_cell_clonality_and_function_from_single_cell_RNA_seq_data Transcriptome Analysis
2018-04-18
EGAS00001002964 Pre_clinical_evolution_of_haematological_malignancies Cancer Genomics
2018-04-18
EGAS00001002965 SNP array data for 140 individuals from 5 populations in Pakistan Other
2018-04-18
EGAS00001002966 Contribution of allelic imbalance to colorectal cancer Other
2018-04-19
EGAS00001002967 Identification of Therapeutic Targets in Rhabdomyosarcoma Through Integrated Genomic, Epigenomic, and Proteomic Analyses Other
2018-04-20
EGAS00001002968 Genomic landscape of IG-MYC positive Burkitt lymphoma with precursor B-cell immunophenotype. Other
2018-04-20
EGAS00001002969 HELIUS cohort Other
2018-04-20
EGAS00001002972 Single cell exome sequencing of lung adenocarcinoma Other
2018-04-24
EGAS00001002975 A genome scan for genes underlying adult body size differences between Central African hunter-gatherers and farmers. Other
2018-04-25
EGAS00001002976 H3Africa Chip Design - Aim of designing a cost-effective GWAS chip with content appropriate for use in genomics studies of individuals from the African continent. Other
2018-04-26
EGAS00001002977 Targeted sequencing about core genes involved in telomere biology in colorectal cancer patients Other
2018-04-27
EGAS00001002979 Targeted sequencing of head and neck squamous cell carcinomas Other
2018-04-27
EGAS00001002980 RNAseq of Follicular Lymphoma Other
2018-04-28
EGAS00001002981 RNA-seq analysis of human primary keratinocytes and skin Other
2018-04-28
EGAS00001002983 Identification of the mutational consequences of precancerous liver disease (including alcohol abuse) on the genomes of human adult stem cells. Other
2018-05-02
EGAS00001002987 The whole blood of female volunteers and sperm from the male volunteer were used to extract genomic DNA to do whole genome sequencing. Distinguished SNPs between parental genomes were retained to analyze parental allele-specific DNA methylation and chromatin accessibility in scCOOL-seq data. Other
2018-05-03
EGAS00001002988 Role_of_HPV_and_Interferon_in_APOBEC_mutational_signature Cancer Genomics
2018-05-03
EGAS00001002991 Interethnic comparability in blood pressure GWAS Other
2018-05-07
EGAS00001002993 A benchmarking resource for NGS testing of cancer predisposition genes Other
2018-05-08
EGAS00001002996 Host whole genome variations are associated with neurocognitive outcome in survivors of pediatric medulloblastoma Other
2018-05-10
EGAS00001002998 Integrated Genomic, Epigenetic, and Expression Analyses of Ovarian Cancer Cell Lines Other
2018-05-14
EGAS00001002999 Pheno-Seq, linking 3D phenotypes of clonal tumor spheroids to gene expression Other
2018-05-14
EGAS00001003001 Spatial Transcriptomics on prostate cancer heterogeneity Other
2018-05-15
EGAS00001003002 Next Generation Children project - WGS study of patients in NICU and PICU and their families Other
2018-05-15
EGAS00001003003 Epigenetic profiling of colorectal cancer initiating cells (CC-ICs) to identify bivalently marked genes (H3K4me3 and H3K27me3 ChIP-seq), and investigation of changes in transcriptome following EZH2 inhibition using RNA-seq. Other
2018-05-15
EGAS00001003004 Genentech study of gallbladder cancer Other
2018-05-16
EGAS00001003006 Genomic profiling of paediatric glioma cell lines Other
2018-05-17
EGAS00001003007 Biallelic tumor suppressor loss and DNA repair defects in de novo small cell prostate cancer Other
2018-05-17
EGAS00001003008 Age-related remodeling of apparently normal esophageal epithelia by common cancer drivers Other
2018-05-18
EGAS00001003010 CTCF/cohesin-binding sites are frequently mutated in cancer Other
2018-05-18
EGAS00001003012 Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___GI___WGS Other
2018-05-18
EGAS00001003014 Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___BD___WGS Other
2018-05-18
EGAS00001003016 H3Africa - Identification and characterization of novel hereditary neurological disease genes in Mali. Other
2018-05-21
EGAS00001003017 Celiac disease-specific intestinal T cells analyzed with HLA-class II tetramers, RNA-seq and mass cytometry have a narrow, autoimmune-associated phenotype Other
2018-05-22
EGAS00001003018 GCAT | Genomes for life: cohort study of the genomes of Catalonia Other
2018-05-22
EGAS00001003021 Somatic_mutation_and_clonal_evolution_in_the_human_testes Cancer Genomics
2018-05-23
EGAS00001003023 Somatic_mutation_and_clonal_evolution_in_the_human_testes___WES Cancer Genomics
2018-05-23
EGAS00001003025 WGS/RNA-seq pair of an inflammatory hepatocellular adenoma (IHCA) Other
2018-05-24
EGAS00001003026 Mutational Signature and Transcriptomic Classification Analyses as the Decisive Diagnostic Tools for a Cancer of Unknown Primary with Neuroendocrine Differentiation Other
2018-05-25
EGAS00001003027 Allele Balance Bias Identifies Systematic Genotyping Errors and False Disease Associations Other
2018-05-25
EGAS00001003028 The evolutionary history of human colitis-associated colorectal cancer Other
2018-05-25
EGAS00001003029 Identification of recurrent mutations in Cushing’s disease Other
2018-05-28
EGAS00001003031 Patient-derived neuroblastoma model system OHC-NB1 Other
2018-05-30
EGAS00001003032 Capture Hi-C on Hodgkin lymphoma cell line L-428 Other
2018-05-31
EGAS00001003033 ChIP-seq data of Hodgkin lymphoma cell line L-428 Other
2018-05-31
EGAS00001003035 AUBTRG - Whole Exome Sequencing of Diffuse Glioma Samples Cancer Genomics
2018-06-02
EGAS00001003038 Recurrent loss of heterozygosity correlates with clinical outcome in pancreatic neuroendocrine cancer Other
2018-06-05
EGAS00001003039 Saliva microbiota in Finnish children Other
2018-06-06
EGAS00001003040 Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations Other
2018-06-06
EGAS00001003043 Evolutionary dynamics of residual disease in human glioblastoma Other
2018-06-06
EGAS00001003044 16S rRNA gene amplification and maternal factors Other
2018-06-06
EGAS00001003047 SPATC1L variants associated with age-related and hereditary hearing loss Other
2018-06-06
EGAS00001003048 Whole exome DNA sequence profiling of spatial biopsies of high grade serous epithelial ovarian cancer Other
2018-06-07
EGAS00001003049 Microdissection_sequencing_of_normal_human_prostate Cancer Genomics
2018-06-07
EGAS00001003053 WES analysis in identifying additive genetic factors that may contribute to the occurrence of moyamoya in neurofibromatosis type 1 Other
2018-06-09
EGAS00001003054 Indonesian Genome Diversity Project Other
2018-06-10
EGAS00001003060 CCND1-negative MCL Other
2018-06-14
EGAS00001003062 Ewings Sarcoma RNA-Seq Other
2018-06-14
EGAS00001003063 Whole Exome Sequencing of 60 tumor/normal matched liver Cancers (HCC) Other
2018-06-15
EGAS00001003064 Histone chaperone CHAF1A promotes proliferation and tumorigenicity in gastric cancer and impacts prognosis via context-depedent regulation of gene expression Other
2018-06-15
EGAS00001003065 Control human putamen and Substantia Nigra Other
2018-06-18
EGAS00001003066 The evolutionary landscape of colorectal tumorigenesis Other
2018-06-19
EGAS00001003068 Somatic mutations reveal lineage relationships and age-related mutagenesis in human hematopoiesis Other
2018-06-19
EGAS00001003070 RNA-seq of Glioblastoma stem cells Other
2018-06-21
EGAS00001003071 Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high risk disease Other
2018-06-22
EGAS00001003072 SLC9A3R1 variant associated with age-related hearing loss Other
2018-06-22
EGAS00001003073 Ovarian cancer organoid biobank Other
2018-06-22
EGAS00001003075 Parallel Detections of Somatic Gene Mutations in Surgically Resected Tumor tissues and Matched Plasma Specimens in Early-Stages of Primary Breast Cancer Other
2018-06-26
EGAS00001003079 RNA sequencing of high hyperdiploid and ETV6/RUNX1-positive pediatric acute lymphoblastic leukemia Other
2018-06-27
EGAS00001003081 Whole-exome ultra-high throughput sequencing in brain samples of suicide victims who had suffered from major depressive disorder and control subjects who had died from other causes. Other
2018-06-27
EGAS00001003085 Exome sequencing in bipolar disorder families Other
2018-06-28
EGAS00001003089 Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___GI___TPS___WGS Other
2018-06-29
EGAS00001003091 HSC_population_dynamics_CBD_samples Cancer Genomics
2018-07-03
EGAS00001003092 Aneurysmal Subarachnoid Hemorrhage patients with or without vasospasm Other
2018-07-03
EGAS00001003093 Genomic and transcriptomic profiling of combined hepatocellular and intrahepatic cholangiocarcinoma reveals distinct molecular subtypes Other
2018-07-03
EGAS00001003094 Bisulphite_MPN_colonies Cancer Genomics
2018-07-04
EGAS00001003095 Somatic mutations in endometriosis and normal uterine endometrium Other
2018-07-04
EGAS00001003096 Whole transcriptome RNA sequencing as comprehensive diagnostic tool for acute myeloid leukemia. Other
2018-07-05
EGAS00001003099 Feasibility Study to Identify the Optimal Adjuvant Combination Scheme of Ipilimumab and Nivolumab (OpACIN) in resectable stage III melanoma patients Other
2018-07-05
EGAS00001003101 Somatic point mutation data from microsatellite unstable colorectal cancers Other
2018-07-06
EGAS00001003103 Study of the rare and low frequency variants in the Saguenay-Lac-Saint-Jean population Other
2018-07-06
EGAS00001003104 Primary plasma cell leukemia (pPCL) samples were sequenced using the Nimblegen MedExome hybridization capture to detect translocations, copy number changes, and mutations in 20 pPCL samples and patient matched controls. Other
2018-07-06
EGAS00001003105 Microbial signatures and innate immune gene expression in lamina propria phagocytes of inflammatory bowel diseases patients Other
2018-07-07
EGAS00001003108 Whole genome amplification and whole genome sequencing of human single cells Other
2018-07-10
EGAS00001003110 Circulating cell-free DNA analysis in Small Cell Lung Cancer Other
2018-07-10
EGAS00001003112 Whole_genome_sequencing_of_in_vitro_colonies Other
2018-07-11
EGAS00001003113 Frequent mutation of the FOXA1 untranslated region in prostate cancer Other
2018-07-12
EGAS00001003114 Reconstruction of human terminal erythroid differentiation cell at single cell level Transcriptome Analysis
2018-07-13
EGAS00001003115 Organoid Models of Human Liver Cancers Derived from Tumor Needle Biopsies Cancer Genomics
2018-07-15
EGAS00001003116 DNA-seq from plasma of 14 liver transplantation patients Other
2018-07-16
EGAS00001003117 BS-seq in plasma of CRC patients Other
2018-07-16
EGAS00001003118 Histone acetylome-wide association study on tuberculosis infection Other
2018-07-17
EGAS00001003119 Low and variable tumor reactivity of the intratumoral TCR repertoire in human cancers Other
2018-07-17
EGAS00001003121 Resolving the Full Spectrum of Human Genome Variation using Linked-Reads Other
2018-07-18
EGAS00001003122 Oesophageal_Adenocarcinoma_Organoid_Hi_C Cancer Genomics
2018-07-19
EGAS00001003123 Heritable pulmonary arterial hypertension in a large Iberian family Other
2018-07-19
EGAS00001003127 Understanding human fetal pancreas development using subpopulation sorting and RNA sequencing Other
2018-07-20
EGAS00001003128 Circular RNA characterization in functionally distinct brain regions Other
2018-07-23
EGAS00001003130 Exome sequencing of advanced hepatocellular carcinoma Other
2018-07-25
EGAS00001003131 WES+WGS OSCCs Boot et al. 2018 Other
2018-07-27
EGAS00001003136 Open_Targets_020_Epigenomes_of_Cell_Lines Epigenetics
2018-07-31
EGAS00001003137 Open_Targets_020_Epigenomes_of_Cell_Lines Epigenetics
2018-07-31
EGAS00001003138 Open_Targets_020_Epigenomes_of_Cell_Lines Transcriptome Analysis
2018-07-31
EGAS00001003139 Open_Targets_020_Epigenomes_of_Cell_Lines Epigenetics
2018-07-31
EGAS00001003140 Automated image-based profiling of complex drug induced phenotypes in patient-derived organoids Other
2018-07-31
EGAS00001003142 Whole exome sequencing of small cell neuroendocrine cancer of the cervix Other
2018-07-31
EGAS00001003144 Single cell sequencing of endoscopic biopsies from Barrett's oesophagus and proximal tissue from the normal GI tract Other
2018-08-01
EGAS00001003145 A comprehensive human gastric cancer organoid biobank captures tumor subtype heterogeneity and enables therapeutic screening Other
2018-08-02
EGAS00001003147 DNA methylomes of monozygotic twins clinically discordant for multiple sclerosis Other
2018-08-02
EGAS00001003148 Copy-choice recombination during mitochondrial L-strand synthesis causes DNA deletions Whole Genome Sequencing
2018-08-03
EGAS00001003151 MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Gastric_Organoids Cancer Genomics
2018-08-08
EGAS00001003154 Sequencing_of_patient_samples_who_received_immune_checkpoint_inhibition___WES___NKI Cancer Genomics
2018-08-09
EGAS00001003157 Partially methylated domains across multiple cell types Other
2018-08-10
EGAS00001003158 DNA Methylation-based diagnostic biomarkers for ESCC in Han Chinese population Other
2018-08-10
EGAS00001003159 Comprehensive genetic analysis of Epstein-Barr virus-associated hematological malignancy Other
2018-08-14
EGAS00001003160 Tumor-associated preferred end coordinates and somatic variants as signatures of circulating tumor DNA Other
2018-08-15
EGAS00001003162 Single_cell_resolution_of_human_CNV_body_map Cancer Genomics
2018-08-15
EGAS00001003163 ChIP-seq data of H3K4me3, H3K27ac and H3K27me3 on multiple human embryonic tissues. Other
2018-08-16
EGAS00001003164 Whole genome sequencing of multiple myeloma identifies novel structural and non-coding mutations. Other
2018-08-16
EGAS00001003165 iNeuron_ChIPseq Other
2018-08-16
EGAS00001003167 Repeated_clinical_malaria_episodes_are_associated_with_modification_of_the_immune_system_in_children_ Transcriptome Analysis
2018-08-20
EGAS00001003168 Primary breast tumor heterogeneity through therapy Cancer Genomics
2018-08-20
EGAS00001003170 Childhood cerebellar tumors mirror conserved fetal transcriptional programs Other
2018-08-21
EGAS00001003171 High Altitude Pulmonary Hypertension Other
2018-08-22
EGAS00001003172 “Castration-persistence” is a distinct state of tolerance to androgen receptor targeting therapies in prostate cancer Other
2018-08-22
EGAS00001003173 Primary breast cancers and paired brain metastases sequencing study Other
2018-08-22
EGAS00001003174 Dnase1l3 knockout causes aberrations in plasma DNA fragmentation Other
2018-08-22
EGAS00001003175 Targeted_sequencing_of_in_vitro_colonies___bulks Cancer Genomics
2018-08-23
EGAS00001003176 Study the differences at the trascriptome level between iNKT and T cells Other
2018-08-24
EGAS00001003177 A Single Complex Agpat2 Allele In A Patient With Partial Lipodystrophy Other
2018-08-27
EGAS00001003178 Neoadjuvant immune checkpoint blockade in high-risk resectable melanoma Other
2018-08-27
EGAS00001003179 Molecular origins of mpMRI visibility Other
2018-08-28
EGAS00001003180 Profiling of Peritoneal Metastases from Gastric Adenocarcinoma Identified Molecular Subtypes Other
2018-08-29
EGAS00001003181 Population_dynamics_in_abnormal_haematopoiesis Other
2018-08-29
EGAS00001003183 ImmunoAgeing_Longitudinal Other
2018-08-30
EGAS00001003184 Analysis of IDHwt-glioblastoma samples from paired primary and recurrent tumor samples Other
2018-08-30
EGAS00001003185 BCR_repertoire_sequencing Resequencing
2018-08-31
EGAS00001003186 The molecular landscape of glioma in patients with Neurofibromatosis 1. Other
2018-08-31
EGAS00001003190 Clonal Decomposition and DNA Replication States Defined by Scaled Single-Cell Genome Sequencing Other
2018-09-05
EGAS00001003191 Oesophageal_Adenocarcinoma_Organoid_10x Cancer Genomics
2018-09-05
EGAS00001003193 Improving CLL Vγ9Vδ2-T cell fitness for cellular therapy by ex vivo activation and ibrutinib Other
2018-09-07
EGAS00001003195 Low frequency and rare coding variation contributes to multiple sclerosis risk Other
2018-09-08
EGAS00001003197 MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__pancreas_LCM_ Cancer Genomics
2018-09-10
EGAS00001003199 Genome-wide association study of cervical cancer in East Asian populations Other
2018-09-11
EGAS00001003200 Exploiting evolutionary steering in cancer therapy Other
2018-09-11
EGAS00001003201 Whole genome and RNAseq analysis of pediatric osteosarcoma Other
2018-09-11
EGAS00001003203 Hyperhaploid Multiple Myeloma Other
2018-09-11
EGAS00001003206 Inference of transcription factor binding from cell-free DNA enables tumor subtype prediction and early detection Other
2018-09-12
EGAS00001003207 Whole exome sequencing of 76 individuals with familial atrial fibrillation Other
2018-09-12
EGAS00001003208 early onset lone atrial fibrillation case-control study Other
2018-09-12
EGAS00001003209 PAX5 biallelic genomic alterations define a novel subgroup of B cell precursor acute lymphoblastic leukemia Other
2018-09-13
EGAS00001003212 Structure and evolution of double minutes in diagnosis and relapse brain tumors Other
2018-09-14
EGAS00001003213 ERBB2/HER2 transmembrane and juxtamembrane domain mutations in cancer Other
2018-09-14
EGAS00001003214 FBSeq: RNA sequencing of human fetal brain. Other
2018-09-15
EGAS00001003215 Single_cell_analysis_of_cytokine_induced_T_cell_states Transcriptome Analysis
2018-09-18
EGAS00001003216 Multiple Sclerosis Replication Chip data (MS Chip) Other
2018-09-18
EGAS00001003217 Fecal Microbiota Transplantation for refractory immune checkpoint inhibitor-associated colitis Other
2018-09-18
EGAS00001003219 Multiple Sclerosis ImmunoChip data Other
2018-09-18
EGAS00001003220 Alternative splicing in Shh-MB Other
2018-09-18
EGAS00001003221 Temporal stability of circulating microRNAs in human serum Other
2018-09-19
EGAS00001003223 Multiple Myeloma Total Therapy trial patient sequencing Other
2018-09-19
EGAS00001003225 Genomic profiling of esthesioneuroblastoma Other
2018-09-20
EGAS00001003227 Whole Exome Sequencing in Multiple Myeloma Other
2018-09-24
EGAS00001003228 Genomic landscape of oral cancers (Illumina WGS) Other
2018-09-24
EGAS00001003231 Gain of function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions Other
2018-09-25
EGAS00001003232 Gain of function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions Other
2018-09-25
EGAS00001003233 Molecular Classification of Lymph Node Metastases Subtypes Predict for Survival in Head and Neck Cancer Transcriptome Analysis
2018-09-26
EGAS00001003234 An exome sequencing approach to defining the genetic risk factors for Achilles tendinopathy Other
2018-09-26
EGAS00001003235 Oncogenic fate conversion by PRDM16s causes acute myeloid leukemia Other
2018-09-26
EGAS00001003236 Discovery of new fusion transcripts in a cohort of pediatric solid cancers at relapse Other
2018-09-26
EGAS00001003237 Genomic landscape of oral cancers (Illumina RNA-Seq) Other
2018-09-26
EGAS00001003238 Fibroblast heterogeneity drives metastatic spread in breast cancer through distinct mechanisms Other
2018-09-28
EGAS00001003239 The malaria-protective human glycophorin structural variant DUP4 shows somatic mosaicism and association with hemoglobin levels Other
2018-10-01
EGAS00001003242 Genomic DNA of tumor tissues, adjacent normal tissues, and peripheral blood were extracted using QIAamp DNA mini Kit (QIAGEN, cat. #51306) Other
2018-10-02
EGAS00001003244 A mechanistic classification of clinical phenotypes in neuroblastoma Other
2018-10-02
EGAS00001003245 Single-cell TCR sequencing of gluten-specific T cells Other
2018-10-02
EGAS00001003247 Characterizing the immune and genome landscapes for osteosarcoma Other
2018-10-02
EGAS00001003248 Epigenetics/genetics of the patient-derived xenografts of pediatric T-cell leukemia Other
2018-10-04
EGAS00001003249 Somatic_mutation_profiling_of_intestinal_crypts_from_IBD_Full_STDY Whole Genome Sequencing
2018-10-04
EGAS00001003250 1 Intratumoral genetic heterogeneity and clonal evolution following neoadjuvant chemoradiotherapy (nCRT) in locally advanced rectal tumors. Other
2018-10-04
EGAS00001003251 Infiltrative and drug-resistant slow-cycling cells support metabolic heterogeneity in glioblastoma Other
2018-10-05
EGAS00001003252 A Study to Evaluate Denosumab in Young Patients With Primary Breast Cancer (D-Beyond) Other
2018-10-08
EGAS00001003254 46 CLL Whole Genome Sequencing Study Other
2018-10-09
EGAS00001003255 Detection of cell-free DNA fragmentation and copy number alterations in cerebrospinal fluid from glioma patients Other
2018-10-09
EGAS00001003256 Molecular Characterization of ETMRs Other
2018-10-09
EGAS00001003257 MYCN Amplification and ATRX Mutations are Incompatible in Neuroblastoma Other
2018-10-09
EGAS00001003258 Enhanced detection of circulating tumor DNA by fragment size analysis Other
2018-10-09
EGAS00001003263 Analysis of translatome, truncating mutations, lncRNA, circRNA and microproteins of 80 human DCM cases and controls Other
2018-10-15
EGAS00001003264 X10_sequencing_of_Oesophageal_Adenocarcinoma_Organoids Cancer Genomics
2018-10-16
EGAS00001003266 Mullighan - PAX5-driven Subtypes Other
2018-10-16
EGAS00001003274 Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - RNA-seq Other
2018-10-18
EGAS00001003275 Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS Other
2018-10-18
EGAS00001003276 Butyrate producers as potential next-generation probiotics: safety assessment of the administration of Butyricicoccus pullicaecorum to healthy volunteers Other
2018-10-18
EGAS00001003278 A GWAS meta-analysis on severe acne on a European population of 26,722 individuals Other
2018-10-22
EGAS00001003280 INSPIRE - Investigator-initiated Phase 2 Study of Pembrolizumab Immunological Response in Metastatic Solid Tumors Cancer Genomics
2018-10-25
EGAS00001003281 Mutations of whole genome sequencing in single cells in normal esophageal epithelium Other
2018-10-29
EGAS00001003282 Paired whole exome sequence of subcutaneous panniculitis-like T-cell lymphoma. Other
2018-10-29
EGAS00001003284 Molecular profiling of longitudinally observed small colorectal polyps: a cohort study Other
2018-10-30
EGAS00001003285 Transcriptome sequencing of Gingivo-buccal Cancer : ICGC-India Project_Batch05 Other
2018-10-30
EGAS00001003286 Androgen deprivation therapy promotes an inflammatory and obesity-like microenvironment in periprostatic fat Other
2018-10-31
EGAS00001003288 Mutated H3 Histones Drive Human Pre-Leukemic Hematopoietic Stem Cell Expansion And Promote Leukemic Aggressiveness Other
2018-11-01
EGAS00001003290 Genomic characterization of metastatic breast cancers Other
2018-11-05
EGAS00001003291 RNA sequencing of undifferentiated sarcomas Other
2018-11-05
EGAS00001003292 Whole Tumor spatial heterogeneity in metastatic melanoma Other
2018-11-05
EGAS00001003293 Pseudotime_ordering_of_cell_cycle_state Cancer Genomics
2018-11-06
EGAS00001003295 SEARCH FOR BACTERIA IN NEURAL TISSUE FROM AMYOTROPHIC LATERAL SCLEROSIS Other
2018-11-07
EGAS00001003296 1054 Flemish Gut Flora Project (FGFP) samples (16S sequencing, dual index) Other
2018-11-07
EGAS00001003297 Placental_genomics Cancer Genomics
2018-11-08
EGAS00001003298 FGFP and TR-MDD shotgun sequencing samples (N=157) Other
2018-11-08
EGAS00001003300 Acquiring and sequencing of all 24 single human chromosomes Other
2018-11-09
EGAS00001003302 Tetralogy of fallot whole-exome sequencing Other
2018-11-10
EGAS00001003303 Genetic alterations in metastatic uveal melanoma Cancer Genomics
2018-11-11
EGAS00001003305 Whole genome sequencing of tumour and matched normal from patients with family history of breast cancer Other
2018-11-13
EGAS00001003306 Personalized RNA mutanome vaccines mobilize poly-specific therapeutic immunity against cancer Other
2018-11-13
EGAS00001003307 Personalized RNA mutanome vaccines mobilize poly-specific therapeutic immunity against cancer RNA-Seq Other
2018-11-13
EGAS00001003309 The analysis of mtDNA variability of the modern Polish population Other
2018-11-13
EGAS00001003310 Adeno-associated virus in the liver: natural history and consequences in tumor development Other
2018-11-13
EGAS00001003311 MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__WG_ Other
2018-11-14
EGAS00001003313 MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__Exome_ Other
2018-11-14
EGAS00001003315 MutWP5__CRUK_Mutographs_of_Cancer__Breast__BRCA_Carriers__Targeted_ Cancer Genomics
2018-11-14
EGAS00001003316 MutWP5__CRUK_Mutographs_of_Cancer__Breast__BRCA_Carriers__Exome_ Cancer Genomics
2018-11-14
EGAS00001003317 MutWP5__CRUK_Mutographs_of_Cancer__Breast__Cancer_Mastectomy__WG_ Cancer Genomics
2018-11-14
EGAS00001003318 MutWP5__CRUK_Mutographs_of_Cancer__Breast__Cancer_Mastectomy__Targeted_ Cancer Genomics
2018-11-14
EGAS00001003319 MutWP5__CRUK_Mutographs_of_Cancer__Breast__Cancer_Mastectomy__Exome_ Cancer Genomics
2018-11-14
EGAS00001003320 MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD37920__WG_ Cancer Genomics
2018-11-14
EGAS00001003321 MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD37920__Targeted_ Cancer Genomics
2018-11-14
EGAS00001003322 MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD38233__WG_ Cancer Genomics
2018-11-14
EGAS00001003324 MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD38234__WG_ Cancer Genomics
2018-11-14
EGAS00001003325 MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD38234__Targeted_ Cancer Genomics
2018-11-14
EGAS00001003329 H014: HES5 mediates NOTCH signaling by interaction with AKT to drive liver carcinogenesis Other
2018-11-15
EGAS00001003331 SNP array datas of 'Matched' cancer/PNE Other
2018-11-15
EGAS00001003332 RNAseq data from human colon organoid infected by KP Other
2018-11-16
EGAS00001003333 RNA-seq of Ewing sarcoma tumors (ICGC) Other
2018-11-19
EGAS00001003335 Genome-wide characterization of Arabian Peninsula populations Other
2018-11-21
EGAS00001003337 Naive B-cell receptor heavy chain repertoire of celiac patients and healthy controls Other
2018-11-21
EGAS00001003341 MGA-NUTM1 fusion in high grade spindle cell sarcoma Other
2018-11-22
EGAS00001003342 WGS and WES of pediatric osteosarcoma Other
2018-11-22
EGAS00001003343 Exome sequencing of a novel cervical cancer cell line Other
2018-11-23
EGAS00001003344 CAF-S3 subset in human breast and ovarian cancers Other
2018-11-26
EGAS00001003345 Small intestinal plasma cells transcriptome profiles Other
2018-11-26
EGAS00001003346 HG Transcriptome sequencing in the INTERVAL cohort Other
2018-11-26
EGAS00001003349 WTCCC2 Pre-eclampsia Study Other
2018-11-28
EGAS00001003350 ALPI deficiency causes refractory Inflammation Bowel Disease Other
2018-11-28
EGAS00001003351 Circulating tumour DNA abundance and potential utility in de novo metastatic prostate cancer Other
2018-11-29
EGAS00001003352 Evaluation of commercial Guardant360 ctDNA test in metastatic prostate cancer Other
2018-11-29
EGAS00001003353 Non-coding RNAs in breast cancer Other
2018-11-29
EGAS00001003354 Neoadjuvant chemotherapy alters the genomic landscape and immune microenvironment of breast cancers Other
2018-11-30
EGAS00001003355 Gene expression in CSF and blood of patients with pneumococcal meningitis RNASeq
2018-11-30
EGAS00001003357 Genomic Profiling of Thyroid Cancer Reveals a Role for Thyroglobulin in Metastasis -Part II Other
2018-12-02
EGAS00001003358 Small intestinal neuroendocrine tumors Other
2018-12-02
EGAS00001003359 Ancient nuclear genomes enable repatriation of Indigenous human remains Other
2018-12-02
EGAS00001003360 organoid data of colorectal cancers Whole Genome Sequencing
2018-12-03
EGAS00001003361 Forty-Five patient-derived xenografts capture the clinical and biological heterogeneity of Wilms tumor Other
2018-12-03
EGAS00001003362 Uveal melanoma patient with germline MBD4 nonsense mutation Other
2018-12-04
EGAS00001003363 Single-cell RNA-seq of immune cells sorted from human melanoma tumors Other
2018-12-04
EGAS00001003365 Finding structural variation from the patient-derived xenografts of pediatric T-cell leukemia at the single-cell level Other
2018-12-05
EGAS00001003366 Microsatellite unstable colorectal cancers Other
2018-12-06
EGAS00001003367 Genomic and transcriptomic determinants of therapy resistance and immune landscape evolution during anti-EGFR treatment in colorectal cancer Other
2018-12-06
EGAS00001003368 Single-cell atlas of the developing brain to investigate the cellular origins of pediatric brain tumors RNASeq
2018-12-06
EGAS00001003369 Pancreatic cancer organoids recapitulate disease and allow personalized drug screening Other
2018-12-07
EGAS00001003370 Mutational Patterns in Metastatic Cutaneous Squamous Cell Carcinoma Other
2018-12-10
EGAS00001003372 Summary statistics from genome-wide association study in glioma of 12,488 cases and 18,169 controls. Other
2018-12-10
EGAS00001003380 PTPN22 SNPs and outcome after lung transplantation Other
2018-12-12
EGAS00001003382 Detection of mutational patterns in cell free DNA (cfDNA) of colorectal cancer by custom amplicon sequencing Other
2018-12-12
EGAS00001003383 ProjectMinE :llumina HiSeqX and HiSeq 2000 whole genome sequence data on 3,001 ALS samples including 212 with known C9orf72 repeat expansions Other
2018-12-12
EGAS00001003384 Lymphocyte_LCM_WGS Cancer Genomics
2018-12-12
EGAS00001003385 Whole genome sequencing of Ewings Sarcoma Other
2018-12-12
EGAS00001003386 Nuclear_single_seq_pilot Cancer Genomics
2018-12-12
EGAS00001003387 Single cell RNA sequencing and Whole Genome Sequencing on different cells from the same sample for a triple negative patient derived xenograft and ovarian cancer cell lines. Other
2018-12-12
EGAS00001003388 Whole-genome sequencing identifies ADGRG6 enhancer mutations and FRS2 duplications as angiogenesis-related drivers in bladder cancer Other
2018-12-13
EGAS00001003396 Hepatocellular carcinoma xenografts established from needle biopsies preserve the characteristics of the originating tumors Transcriptome Analysis
2018-12-17
EGAS00001003397 HSC_population_dynamics___CB001_samples Cancer Genomics
2018-12-17
EGAS00001003399 Familial Myeloid Leukemia Other
2018-12-17
EGAS00001003400 Whole-exome sequencing of NTHL1 deficient tumors Exome Sequencing
2018-12-18
EGAS00001003405 KIT-dependent and -independent genomic heterogeneity of resistance in gastrointestinal stromal tumors - TORC1/2 inhibition as salvage strategy Other
2018-12-19
EGAS00001003406 Sequencing Study in COPD cases and controls Other
2018-12-19
EGAS00001003407 Utility of ctDNA to support patient selection for early phase clinical trials: The TARGET Study Other
2018-12-21
EGAS00001003408 Methylation analysis of plasma DNA informs etiologies of Epstein-Barr virus-associated diseases Other
2018-12-26
EGAS00001003409 Plasma DNA motif analysis Other
2018-12-26
EGAS00001003411 RNA sequencing of multiple myeloma identifies genes dysregulated by structural variants. Other
2018-12-27
EGAS00001003412 Altered oligodendrocyte heterogeneity in Multiple sclerosis revealed by single nuclei RNA sequencing Other
2018-12-31
EGAS00001003414 Mutation tracking in single cell RNA-Seq reveals consequences of subclonal evolution in acute myeloid leukemia Other
2019-01-02
EGAS00001003415 Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements Other
2019-01-02
EGAS00001003418 Landscape of somatic mutations and DNA copy number alterations and transcriptomic profiling identifies metabolic reprogramming as a hallmark of ibrutinib resistance Other
2019-01-08
EGAS00001003419 16S-based fecal microbiota composition of the Milieu Intérieur Cohort Other
2019-01-08
EGAS00001003421 STREP GENE: Genetics and Severe Streptococcal Infections Other
2019-01-09
EGAS00001003423 Study the genetic susceptibility of esophagus squamous cell carcinomas (ESCC) in high-risk area Henan Chinese Other
2019-01-11
EGAS00001003424 Genome Wide Association Study:GR@ACE Stage I Other
2019-01-14
EGAS00001003425 the Yemeni-Somali 5 million SNP array dataset Other
2019-01-14
EGAS00001003426 Panel-based next-generation sequencing study of human liver samples. Other
2019-01-14
EGAS00001003427 Combined MEK and BCL-2/XL inhibition is effective in high-grade serous ovarian cancer patient-derived xenograft models and BIM levels are predictive of responsiveness Other
2019-01-15
EGAS00001003428 Genomic_profiling_of_B_other_Adult_ALL_RNA Other
2019-01-16
EGAS00001003430 Clinical genome sequencing uncovers potentially targetable truncations and fusions of MAP3K8 in spitzoid and other melanomas Other
2019-01-16
EGAS00001003432 Whole genome sequencing with linked reads of pediatric glioblastoma samples Other
2019-01-17
EGAS00001003433 Somatic_mutation_and_clonal_evolution_in_the_human_bladder_Novaseq Whole Genome Sequencing
2019-01-18
EGAS00001003434 Extreme intratumor heterogeneity and driver evolution in mismatch repair deficient gastro-esophageal cancer Cancer Genomics
2019-01-21
EGAS00001003436 SHANK2 mutations associated with Autism Spectrum Disorder cause hyperconnectivity of human neurons Other
2019-01-21
EGAS00001003437 Paediatric Tumour Profiling Other
2019-01-21
EGAS00001003438 Intratumoural Heterogeneity Underlies Distinct Therapy Responses and Treatment Resistance in Glioblastoma Other
2019-01-22
EGAS00001003439 Multi-region exome sequencing of lung adenocarcinoma precursors -1 Other
2019-01-22
EGAS00001003442 Functional and genomic heterogeneity of long-term self-renewing compartment as the origin of treatment resistance in pancreatic tumors Other
2019-01-23
EGAS00001003443 Reconstituting the transcriptome and DNA methylome landscapes of human implantation at single-cell resolution Other
2019-01-24
EGAS00001003444 Analysis of error profiles in deep next-generation sequencing data Other
2019-01-24
EGAS00001003445 Orphan_Tumour_Study_NB Transcriptome Analysis
2019-01-25
EGAS00001003446 Liver_Tumours_WGS Whole Genome Sequencing
2019-01-25
EGAS00001003447 Clonal architectures predict clinical outcome in clear cell renal cell carcinoma Other
2019-01-26
EGAS00001003449 Single-cell RNA sequencing on single CD45+ immune cells isolated from peripheral blood, lymphnode, ascites, tumour and adjacent normal tissues from six hepatocellular carcinoma patients. Other
2019-01-27
EGAS00001003450 MCO colorectal cancer genomics at UNSW Other
2019-01-28
EGAS00001003451 RNA-seq of M-CSF differentiated human peripheral monocyte-derived macrophages (MDMs) - Validation macIDR Other
2019-01-28
EGAS00001003452 Probabilistic cell type assignment of single-cell transcriptomic data reveals spatiotemporal microenvironment dynamics in human cancers Other
2019-01-28
EGAS00001003453 Molecular profiling of blastic plasmacytoid dendritic cell neoplasm (BPDCN) as compared to acute myeloid leukemia (AML) Other
2019-01-29
EGAS00001003454 Molecular Phenotype of Constitutional TET2 Haploinsufficiency in Humans Other
2019-01-31
EGAS00001003455 MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal_LCM Whole Genome Sequencing
2019-01-31
EGAS00001003456 Somatic_mutation_and_clonal_evolution_in_the_human_bladder_WES_NOVASEQ Other
2019-01-31
EGAS00001003457 GermCellTumour Whole Genome Sequencing
2019-02-01
EGAS00001003458 TRACERx 100: RNAseq data from the first 100 TRACERx tumours Other
2019-02-01
EGAS00001003460 GWAS and Meta-analysis on Frontal Fibrosing Alopecia in two European Populations Other
2019-02-05
EGAS00001003462 Whole genome sequencing of 25 South African individuals with myasthenia gravis Other
2019-02-07
EGAS00001003463 Exome sequencing of stroke cases with good or bad recovery three months after stroke Other
2019-02-08
EGAS00001003465 Identification_of_immune_mechanisms_associated_with_the_high_rate_of_relapse_in_patient_with_visceral_leishmaniasis_and_HIV_co_infection Transcriptome Analysis
2019-02-11
EGAS00001003467 Placental multi-omics data-mining in Intra-Uterine Growth Restriction Other
2019-02-11
EGAS00001003468 Adenoma to Carcinoma transition in Colorectal Cancer Other
2019-02-12
EGAS00001003469 We evaluate the potential for routine WGS using ONT by sequencing the well-characterised reference sample NA12878 and the genome of an individual with ataxia-pancytopenia syndrome accompanied by severe immune dysregulation. Other
2019-02-12
EGAS00001003471 Dedifferentiated_Melanoma Cancer Genomics
2019-02-13
EGAS00001003474 Exome sequencing of synchronous colorectal cancers Other
2019-02-14
EGAS00001003479 Single_cell_analysis_T_cell_activation Other
2019-02-15
EGAS00001003481 Mutational patterns and regulatory networks in epigenetic subgroups of meningioma (H033) Other
2019-02-15
EGAS00001003484 TRACERx 100: RRBS data from a subset of the first 100 TRACERx tumours Other
2019-02-18
EGAS00001003485 Chromatin 3D interactions mediate genetic effects on gene expression Other
2019-02-18
EGAS00001003486 Mutational landscape of the transcriptome offers putative targets for immunotherapy of myeloproliferative neoplasms Other
2019-02-18
EGAS00001003487 Combined gene expression and digital pathology identifies molecular mediators of T cell exclusion and immune suppression in ovarian cancer Other
2019-02-20
EGAS00001003488 Growth Hormone (GH) -secreting Pituitary Adenoma Other
2019-02-20
EGAS00001003489 Molecular phenotyping of MCA/ID patients to improve diagnosis Other
2019-02-20
EGAS00001003490 Predicting brain tumor recurrence: development and validation of a DNA-methylation based nomogram in meningioma Other
2019-02-20
EGAS00001003493 High-resolution structural genomics reveals new therapeutic vulnerabilities in glioblastoma Other
2019-02-20
EGAS00001003496 Somatic mutations increase hepatic clonal fitness and regeneration in chronic liver disease Other
2019-02-21
EGAS00001003497 Genomic stratification and liquid biopsy in a rare adrenocortical carcinoma (ACC) case, with dual lung metastases Other
2019-02-22
EGAS00001003498 DIME study: Safety, dose-response and efficacy of treatment with Anaerobutyricum soehgenii on glucose metabolism in human subjects with metabolic syndrome Other
2019-02-22
EGAS00001003499 EXCEED Study Other
2019-02-24
EGAS00001003500 Whole-genome sequencing of Tibetans from China Other
2019-02-25
EGAS00001003501 Chromatin_accessability_in_cytokine_induced_immune_cell_states Epigenetics
2019-02-26
EGAS00001003502 MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD43291_Novaseq__WG_ Other
2019-02-26
EGAS00001003503 MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD43291_Novaseq__Exome_ Other
2019-02-26
EGAS00001003504 Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data Other
2019-02-27
EGAS00001003506 Analysis of Multiparametric MR imaging and tumor tissue sampling to identify response and acquired resistance to HIF-2 inhibition in patients with advanced clear cell renal cell carcinoma enrolled in a phase 1, multiple-dose, dose-escalation trial of PT2385, a HIF-2alpha inhibitor Cancer Genomics
2019-02-27
EGAS00001003507 Fixation effects on variant-calling in a clinical resequencing panel Other
2019-02-28
EGAS00001003508 300-Obese: clinical cohort of obese individuals, Nijmegen, the Netherlands Other
2019-03-01
EGAS00001003510 Juvenile Idiopathic Arthritis exome sequencing in a consanguineous family Other
2019-03-03
EGAS00001003511 The Medical Genome Reference Bank: a whole genome data resource of 4,000 healthy elderly individuals. Other
2019-03-04
EGAS00001003512 whole-genome sequencing of gastric cancer Other
2019-03-04
EGAS00001003513 Comparison of 3 protocols for deriving pancreatic progenitors from hPSC with RNA-seq and ATAC-seq Other
2019-03-04
EGAS00001003514 The biology of cell-free DNA fragmentation and the roles ofDNASE1, DNASE1L3 and DFFB Other
2019-03-05
EGAS00001003515 Gene regulation of human stimulated and cultured CD4+ Treg cells Other
2019-03-05
EGAS00001003516 Gene_regulation_of_human_CD4__Treg_cells_ Other
2019-03-05
EGAS00001003517 Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___DNA_sequencing Whole Genome Sequencing
2019-03-07
EGAS00001003519 Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___single_cell_RNA_sequencing Transcriptome Analysis
2019-03-07
EGAS00001003520 MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Pancreatic_Organoids Whole Genome Sequencing
2019-03-08
EGAS00001003521 Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants Other
2019-03-09
EGAS00001003523 MutWP5__CRUK_Mutographs_of_Cancer__BRCA_Carriers___WG__Novaseq_ Other
2019-03-11
EGAS00001003524 MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___WG__Novaseq_ Other
2019-03-11
EGAS00001003525 MutWP5__CRUK_Mutographs_of_Cancer__Cancer_Mastectomy__WG__Novaseq_ Whole Genome Sequencing
2019-03-11
EGAS00001003526 MutWP5__CRUK_Mutographs_of_Cancer__BRCA_Carriers___Exome__Novaseq_ Other
2019-03-11
EGAS00001003527 MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___Exome__Novaseq_ Other
2019-03-11
EGAS00001003528 MutWP5__CRUK_Mutographs_of_Cancer__Cancer_Mastectomy__Exome__Novaseq_ Other
2019-03-11
EGAS00001003530 Comprehensive characterization of cell-free tumor DNA in plasma and urine of patients with renal tumors Other
2019-03-12
EGAS00001003531 Melanoma_post_mortem_analysis Cancer Genomics
2019-03-13
EGAS00001003532 Sequencing of Infant high grade gliomas Other
2019-03-13
EGAS00001003534 The landscape of LAM disease Other
2019-03-14
EGAS00001003535 Immune induction strategies to enhance the sensitivity to PD-1 blockade in metastatic triple negative breast cancer: the TONIC-trial Other
2019-03-14
EGAS00001003536 Tumor-derived cell lines as pharmacogenomic models to predict therapeutic vulnerabilities in hepatocellular carcinoma Other
2019-03-15
EGAS00001003538 Whole_Genome_Sequencing_of_Human_Organoid_Lines Cancer Genomics
2019-03-15
EGAS00001003539 Clonal evolution in myeloma: the impact of maintenance lenalidomide and depth of response on the genetics and sub-clonal structure of relapsed disease in uniformly treated newly diagnosed patients Other
2019-03-15
EGAS00001003540 Genomic and transcriptomic landscape of aggressive thyroid cancer Other
2019-03-16
EGAS00001003541 Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___UGI___WGS Other
2019-03-18
EGAS00001003542 MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma___2 Other
2019-03-18
EGAS00001003544 RNA sequencing of NK cells in human lung Other
2019-03-18
EGAS00001003545 Genomics analysis of mucinous tumours of the ovary and related neoplasms Other
2019-03-19
EGAS00001003546 Evolution of GBM through therapy Other
2019-03-20
EGAS00001003547 Germline variants collaborate with somatic mutations and initiate and/or drive disease in primary myelodysplastic syndrome (MDS) and therapy-related myeloid neoplasms (t-MN) Cancer Genomics
2019-03-20
EGAS00001003548 Rare coding variants in lupus risk genes Other
2019-03-21
EGAS00001003549 Placental_mosaicism Cancer Genomics
2019-03-21
EGAS00001003550 HSC_population_dynamics___KX003_samples Whole Genome Sequencing
2019-03-21
EGAS00001003553 To_profile_the_landscape_of_sebaceous_tumours_WES Cancer Genomics
2019-03-22
EGAS00001003554 Arriba: accurate and efficient detection of gene fusions from RNA-Seq (H021) Other
2019-03-22
EGAS00001003555 Revealing active mutational processes in tumours using DigiPico/MutLX at unprecedented accuracy Other
2019-03-24
EGAS00001003556 Pharmacogenomic analysis of patient-derived tumor cells in gynecologic cancers Other
2019-03-25
EGAS00001003558 Colorectal cancer organoids expressing BRAF (fusion) genes Other
2019-03-26
EGAS00001003560 Genetic modification of primary human B cells to model high-grade lymphoma RNASeq
2019-03-27
EGAS00001003563 Genetic Alterations in Benign Breast Biopsies of Subsequent Breast Cancer Patients Other
2019-03-29
EGAS00001003564 Probabilistic modeling of personalized drug combinations from integrated chemical screen and molecular data in sarcoma Other
2019-03-30
EGAS00001003565 South Asia Rheumatic Heart Disease Genetics Network Other
2019-04-01
EGAS00001003570 Whole-genome sequencing of normal Singaporean volunteers Population Genomics
2019-04-03
EGAS00001003571 Understanding_Self__Organising_Capacity_of_Stem_Cells_during_Implantation_and_Early_Post_implantation_Development_in_vitro_and_in_vivo__Implications_for_Human_Development_ Transcriptome Analysis
2019-04-03
EGAS00001003572 Pervasive H3K27 acetylation and ERV expression in H3.3K27M gliomas present a therapeutic vulnerability Other
2019-04-03
EGAS00001003573 Multi-Region WES of Metastatic Colorectal Cancer Cancer Genomics
2019-04-03
EGAS00001003575 RNA-sequencing of adult T-cell leukemia/lymphoma samples Other
2019-04-04
EGAS00001003576 Cancer-Associated Mutations in Endometriosis without Cancer Other
2019-04-04
EGAS00001003579 Analysis of four key cell types (epithelial, fbroblast, myeloid and T cells) Other
2019-04-05
EGAS00001003582 Phylogenetic evolution of metastatic melanoma. Other
2019-04-08
EGAS00001003583 Genetic dysregulation of gene expression and splicing during a ten-year period of human aging in the PIVUS study Other
2019-04-09
EGAS00001003585 Gut microbiota analysis after 3months probiotic-like bacteria or placebo treatment in subjects with metabolic syndrome Other
2019-04-09
EGAS00001003586 Disease and phenotype relevant genetic variants identified from histone acetylomes in human hearts Other
2019-04-09
EGAS00001003590 Investigation of human variation in healthy individuals on gene and protein levels Other
2019-04-10
EGAS00001003592 5- FU treated organoids Other
2019-04-12
EGAS00001003594 Lymphocyte_Gut_WGS_H38 Whole Genome Sequencing
2019-04-12
EGAS00001003596 Lymphocyte_PanBody_WGS_H38 Whole Genome Sequencing
2019-04-12
EGAS00001003598 Single cell transcriptomic and genomic profiling of carcinogenesis in patients with familial adenomatous polyposis Other
2019-04-15
EGAS00001003599 Whole exome sequencing of trio with primary immunodeficiency (IL2RB) Other
2019-04-15
EGAS00001003600 Quantitative microbiome profiling disentangles inflammation- and bile duct obstruction-associated microbiota alterations across IBD/PSC diagnoses Other
2019-04-16
EGAS00001003601 Dedifferentiated_Melanoma_RNAseq Cancer Genomics
2019-04-17
EGAS00001003602 GDAP___Genome_Diversity_in_Africa_Project Whole Genome Sequencing
2019-04-18
EGAS00001003603 Genetic and expression landscape of Waldenstrom macroglobulinemia Other
2019-04-18
EGAS00001003605 A Phase II Trial of High Dose Interleukin-2 and Multi-site Stereotactic Ablative Radiotherapy for Patients with Metastatic Renal Cell Carcinoma Other
2019-04-18
EGAS00001003607 GWAS Steroid Sensitive Nephrotic Syndrome Population Genomics
2019-04-22
EGAS00001003611 Genome-wide cell-free DNA fragmentation in patients with cancer Other
2019-04-24
EGAS00001003616 Kidney_tumour_DNA_exome Other
2019-04-26
EGAS00001003617 Discovery and capture of novel dynamic DNA methylation in human sperm with preferential links to altered folate metabolism Other
2019-04-26
EGAS00001003620 Recapitulation of genetic predisposition to medulloblastoma in human neuroepithelial stem cells Other
2019-04-26
EGAS00001003623 Novel PARN mutations in Hoyeraal-HReidarsson syndrome patients. Other
2019-04-29
EGAS00001003624 WGS of Roma (Romani/Rroma) and European/Romanian individuals from Romania Other
2019-04-29
EGAS00001003626 Mutations conferring differential treatment response in breast cancer Other
2019-04-29
EGAS00001003627 Synthetic modeling reveals HOXB genes are critical for the initiation and maintenance of human leukemia Epigenetics
2019-04-30
EGAS00001003628 Oral mucosa organoids as a potential model for personalized therapies Other
2019-04-30
EGAS00001003629 UAMS Smoldering Myeloma Myeloma Sequencing Other
2019-04-30
EGAS00001003631 Breast Cancer - immune clusters - RNA-seq Other
2019-04-30
EGAS00001003633 CRC GWAS on the Spanish population Other
2019-05-02
EGAS00001003634 Non-invasive prenatal diagnosis by genome-wide haplotyping of maternal cell-free plasma DNA Other
2019-05-02
EGAS00001003635 Genome‐wide postnatal changes in immunity following fetal inflammatory response Other
2019-05-02
EGAS00001003638 Effect of 28-day administration of Urolithin A to sedentary elderly on muscle gene expression Other
2019-05-03
EGAS00001003639 Genome-wide search to find the genetic elements underlying visual contour perception Other
2019-05-04
EGAS00001003642 Pangenomic classification of pituitary adenomas Other
2019-05-07
EGAS00001003643 Presence of bacterial infection in brains of patients with Parkinson's disease (PD) Other
2019-05-07
EGAS00001003644 Presence of fungal infection in brains of patients with Parkinsons disease (PD) Other
2019-05-07
EGAS00001003645 GWAS Results from Danjou et al, Nature Genetics 2015 Other
2019-05-07
EGAS00001003646 Latency and interval therapy affect the evolution in metastatic colorectal cancer Other
2019-05-07
EGAS00001003647 Mapping_genetic_variants_underlying_gene_regulation_in_healthy_intestinal_cell_types_to_identify_novel_IBD_drug_targets Transcriptome Analysis
2019-05-08
EGAS00001003648 Whole genome sequencing of six ethnic groups from Burkina Faso, Cameroon, and Tanzania Other
2019-05-08
EGAS00001003650 WGBS analysis corresponding to representative cases of iBCP-ALL patients Other
2019-05-10
EGAS00001003651 multi-OMICs study of a pair of infant monozygotic twins with concordant B-cell ALL Other
2019-05-12
EGAS00001003652 Accelerated clonal evolution in refractory versus relapsed chronic lymphocytic leukemia upon treatment Other
2019-05-13
EGAS00001003653 Indonesian methylation data Other
2019-05-15
EGAS00001003654 Indonesian Genome Diversity Project 2 Other
2019-05-16
EGAS00001003656 Healthspan and lifespan extension by fecal microbiota transplantation in progeroid mice Other
2019-05-17
EGAS00001003657 Human pan-genome analysis Other
2019-05-18
EGAS00001003658 Epitope-linked Ig-seq of self-reactive plasma cells in celiac disease Transcriptome Analysis
2019-05-20
EGAS00001003659 Genomic Signatures Reveal DNA Damage Response Deficiency in Brain Metastases of Colorectal Cancer Other
2019-05-20
EGAS00001003660 Whole-genome and transcriptome sequencing of blastic plasmacytoid dendritic cell neoplasm Cancer Genomics
2019-05-20
EGAS00001003661 Bioinformatic Methods and Bridging of Assay Results for Reliable Tumor Mutational Burden Assessment in Non-Small Cell Lung Cancer Other
2019-05-21
EGAS00001003662 Combined genetic and transcriptome analysis of patients with Systemic Lupus Erythematosus (SLE) Other
2019-05-21
EGAS00001003663 Massively parallel single-cell B-cell receptor sequencing enables rapid discovery of diverse antigen-reactive antibodies Other
2019-05-22
EGAS00001003667 RNA-seq as a tool for evaluating human embryo competence Other
2019-05-23
EGAS00001003670 Indonesian Genome Diversity Project 2, genotyping data Other
2019-05-27
EGAS00001003671 Indonesian RNA-seq data Other
2019-05-27
EGAS00001003672 Molecular Profiling Reveals Unique Immune and Metabolic Features of Melanoma Brain Metastases Other
2019-05-27
EGAS00001003673 Single-cell TCR sequencing of DQ2.2-glut-L1-specific T cells Other
2019-05-28
EGAS00001003674 Single-cell TCR sequencing of DQ2.5-hor-3-specific T cells Other
2019-05-28
EGAS00001003676 Resident memory CD8 T cells persist for years in human small intestine Other
2019-05-28
EGAS00001003678 Presence of bacterial infection in brains of patients with Huntington's disease (HD) Other
2019-05-30
EGAS00001003679 Next Generation Sequencing Characterization of Hematopoietic Stem and Progenitors Cells in Human Systemic Lupus Eryhtematosus RNASeq
2019-05-30
EGAS00001003680 Whole exome sequencing for primary lung adenocarcinoma samples Other
2019-05-31
EGAS00001003681 Single cell RNA sequencing of lung adenocarcinoma. Other
2019-05-31
EGAS00001003682 Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___POL___WGS Cancer Genomics
2019-05-31
EGAS00001003684 Control iPSC lines with clinically annotated genetic variants for versatile multi-lineage differentiation Other
2019-05-31
EGAS00001003685 RNA-sequençing of 21 inflammatory hepatocellular adenomas Other
2019-05-31
EGAS00001003686 Whole Exome Sequencing of 15 Tumor/Normal pairs of inflammatory hepatocellular adenomas Other
2019-05-31
EGAS00001003687 UAMS Smoldering Myeloma Timeline Cohort Other
2019-05-31
EGAS00001003688 HSC_population_dynamics___TG001_2_samples Whole Genome Sequencing
2019-06-03
EGAS00001003689 Large-scale viral genome analysis identifies novel clinical associations between hepatitis B virus and chronically infected patients Other
2019-06-04
EGAS00001003690 Analysis of copy number variation landscape of glioma by shallow coverage whole genome sequencing Other
2019-06-04
EGAS00001003695 Detecting and tracking circulating tumour DNA copy number profiles during first line chemotherapy in oesophagogastric adenocarcinoma Other
2019-06-05
EGAS00001003696 Whole-exome sequencing of acute erythroid leukemia Other
2019-06-06
EGAS00001003698 Breast_cancer_topographs Other
2019-06-07
EGAS00001003699 Integrative and comparative genomic analyses identify clinically relevant groups of pulmonary carcinoids and unveil the supra-carcinoids Other
2019-06-07
EGAS00001003700 GBM cancer stem cell lines -RNA-seq and WGS data Other
2019-06-07
EGAS00001003701 Transcriptome Analysis Offers a Comprehensive Illustration of the Genetic Background of Pediatric Acute Myeloid Leukemia RNASeq
2019-06-08
EGAS00001003702 MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_adenocarcinoma Whole Genome Sequencing
2019-06-10
EGAS00001003703 Renal_habitat_WXS Other
2019-06-10
EGAS00001003705 Multi-layered molecular characterization defines prognostic subtypes of lung adenocarcinoma in Asian never-smokers Other
2019-06-11
EGAS00001003709 Analysis of the genomic landscape of chemoresistant multiple myeloma Exome Sequencing
2019-06-11
EGAS00001003710 The 3D evolution of glioma cell populations Other
2019-06-12
EGAS00001003711 ID1 in glioblastoma Cancer Genomics
2019-06-13
EGAS00001003714 Infant Glioma Molecular Subtype Other
2019-06-13
EGAS00001003715 Characterization of patient-derived xenograft models of myxoid liposarcoma either sentitive or resistant to trabectedin Other
2019-06-13
EGAS00001003719 Sporadic and endemic Burkitt lymphoma have frequent FOXO1 mutations but distinct hotspots in the AKT recognition motif Other
2019-06-18
EGAS00001003722 Exome and Whole-Genome Sequencing of Central African Hunter-Gatherers and Agriculturalists Other
2019-06-19
EGAS00001003723 Cancer and germline exomes consisting of FASTQ paired-end reads from melanoma and lung cancer samples Other
2019-06-19
EGAS00001003724 RNA-seq consisting of FASTQ paired-end reads from cancer samples Other
2019-06-19
EGAS00001003725 Human adipose tissue immune cells Other
2019-06-20
EGAS00001003726 RNA Sequencing of paediatric patients with B lymphoblastic leukemia Other
2019-06-20
EGAS00001003727 From matrimonial practices to genetic diversity in Southeast Asian populations: the signature of the matrilineal puzzle Other
2019-06-21
EGAS00001003730 Genomic, transcriptomic and epigenomic profiling of GCTB Other
2019-06-26
EGAS00001003731 DNA Methylation loss coupled with mitotic cell division promotes immune evasion of tumours with high mutation load Other
2019-06-26
EGAS00001003732 Measuring minimal residual disease in acute myeloid leukemia with MASQ Cancer Genomics
2019-06-26
EGAS00001003733 Analysis of mechanisms of CD19- relapse following novel low affinity CD19 Chimeric Antigen Receptor (CAR) T-cells (CD19 CAR T-cells) in a Phase I clinical study in paediatric ALL: CARPALL Other
2019-06-26
EGAS00001003734 CD3 bispecific antibody-induced cytokine release is dispensable for cytotoxic T cell activity Transcriptome Analysis
2019-06-26
EGAS00001003735 Gene expression by RNAseq in bronchial biopsies of asthmatics, asthma in remission and healthy subjects Other
2019-06-27
EGAS00001003736 Germline mutations in the transcription factor IKZF5 cause thrombocytopenia. Other
2019-06-27
EGAS00001003737 A targeted gene panel that covers coding, noncoding, and short tandem repeat regions improves the diagnosis of patients with neurodegenerative diseases Other
2019-06-28
EGAS00001003738 RNA-seq from human embryonic tissues (additional samples 2018) Other
2019-06-28
EGAS00001003739 DNA methylation in bronchial biopsies of asthmatics, asthma in remission and healthy subjects Other
2019-06-28
EGAS00001003740 Genomics_of_acral_lentiginous_melanoma Other
2019-06-28
EGAS00001003743 HSC_population_dynamics___CB002_samples Whole Genome Sequencing
2019-07-01
EGAS00001003744 Single_cell_HSC_colony_WGS_many_years_post_allogeneic_bone_marrow_transplant Whole Genome Sequencing
2019-07-01
EGAS00001003745 Reference exome data for Australian Aboriginal populations to support health-based research Other
2019-07-02
EGAS00001003746 Integrative genomic analysis identifies key pathogenic mechanisms in primary mediastinal large B-cell lymphoma Other
2019-07-02
EGAS00001003747 Gene expression profile of mesothelial-derived carcinoma-associated fibroblasts Other
2019-07-03
EGAS00001003748 COMPARE study: participants typed during UK Biobank version 2 array development phase Other
2019-07-03
EGAS00001003750 Glioblastoma initiating cells are sensitive to histone demethylase inhibition due to epigenetic deregulation Other
2019-07-05
EGAS00001003751 Single cell transcriptomic analysis of the immune cell compartment in the human small intestine and in Celiac disease Other
2019-07-05
EGAS00001003753 Dissociation of solid tumour tissues with cold active protease for single-cell RNA-seq minimizes conserved collagenase-associated stress responses Other
2019-07-08
EGAS00001003754 Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___POL___TGS_ Other
2019-07-09
EGAS00001003755 High intensity sequencing of plasma cfDNA and WBC gDNA Other
2019-07-10
EGAS00001003756 RNA-seq of cultured human hematopoietic stem and progenitor cells from umblical cord blood in cytokine-rich ex vivo culture conditions following sphingolipid modulation Other
2019-07-10
EGAS00001003760 Genetics and transcriptomes of pediatric B cell precursor leukemia with gain of chromosome 21 Other
2019-07-12
EGAS00001003763 Landscape and significance of multiple mutations in oncogenes. Other
2019-07-16
EGAS00001003764 WES of mCRC xenografts under cetuximab treatment, placebo or after treatment release Other
2019-07-17
EGAS00001003765 RNAseq of mCRC xenografts under cetuximab treatment, placebo or after treatment release Other
2019-07-17
EGAS00001003766 Diverse_outcomes_of_controlled_human_malaria_infection_originate_from_host_intrinsic_immune_variation_and_not_var_gene_switching Transcriptome Analysis
2019-07-17
EGAS00001003767 IBD-dysplasia Cancer Genomics
2019-07-18
EGAS00001003768 HSC_population_dynamics___KX004_samples___WGS Whole Genome Sequencing
2019-07-19
EGAS00001003769 Fresh vs. frozen cell preparations of colorectal cancer single-cell RNA sequencing RNASeq
2019-07-21
EGAS00001003772 The_Genomic_Advances_in_Sepsis__GAinS__RNA_seq Other
2019-07-23
EGAS00001003774 MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal Whole Genome Sequencing
2019-07-25
EGAS00001003775 Whole genome and whole transcriptome sequencing of Hepatosplenic T Cell Lymphoma tumor. Other
2019-07-26
EGAS00001003776 Targetable ERBB2 Mutations in Neurofibroma/Schwannoma Hybrid Nerve Sheath Tumors Cancer Genomics
2019-07-26
EGAS00001003778 The whole genome landscape of Burkitt lymphoma subtypes Other
2019-07-26
EGAS00001003779 Single cell RNA sequencing of 33 primary colorectal cancer RNASeq
2019-07-28
EGAS00001003780 Extreme phenotypes define epigenetic and metabolic signatures in cardiovascular diseases. Other
2019-07-29
EGAS00001003781 WXS of 147 lung cancer patients treated with immunotherapy Other
2019-07-30
EGAS00001003784 Polyomavirus-positive Merkel cell carcinoma derived from a trichoblastoma suggests an epithelial origin of Merkel cell carcinoma Cancer Genomics
2019-08-01
EGAS00001003785 Gene expression from human iPSC derived motor neurons. Other
2019-08-01
EGAS00001003786 Patient-Derived Lung Cancer Organoid Other
2019-08-01
EGAS00001003787 The coding and non-coding transcriptional landscape of subependymal giant cell astrocytomas Other
2019-08-01
EGAS00001003789 'KOREAN' never-smoker female adenocarcinoma RNA-seq Other
2019-08-02
EGAS00001003790 Transcriptional changes in GBM through therapy Other
2019-08-02
EGAS00001003791 Cell-free DNA analysis reveals POLR1D-mediated resistance to bevacizumab in colorectal cancer Other
2019-08-02
EGAS00001003792 Distinct Phenotypes of Human Intrahepatic and Extrahepatic Bile duct Organoids and their Applications for Biliary Disease Modeling Transcriptome Analysis
2019-08-02
EGAS00001003798 Molecular profiling reclassifies adult astroblastoma into known and clinically distinct tumor entities with frequent MAPK pathway alterations Cancer Genomics
2019-08-08
EGAS00001003800 Methylation CYLD cutaneous syndrome Other
2019-08-08
EGAS00001003801 Ulcerative colitis study - WES data Other
2019-08-09
EGAS00001003802 Ulcerative colitis study - RNAseq data Other
2019-08-09
EGAS00001003803 Spatial Heterogeneity in CLL Other
2019-08-09
EGAS00001003804 Comprehensive molecular profiling of high-grade serous ovarian cancer Other
2019-08-12
EGAS00001003805 Celiac disease meta-analysis Other
2019-08-13
EGAS00001003806 Integration of intra-sample contextual error modeling for improved detection of somatic mutations Cancer Genomics
2019-08-13
EGAS00001003809 Whole-exome sequencing of Fanconi anemia-like inherited bone marrow failure syndrome Other
2019-08-14
EGAS00001003812 Single cell sequencing: Capturing the origin and dynamics of chromosomal copy-number heterogeneity Cancer Genomics
2019-08-16
EGAS00001003813 The Precision Medicine in Liver Cancer across an Asia-pacific NETwork (PLANET) Other
2019-08-19
EGAS00001003814 The Precision Medicine in Liver Cancer across an Asia-pacific NETwork (PLANET) - Intratumoural immune heterogeneity Other
2019-08-19
EGAS00001003816 Epigenetic and metabolomic data from type 2 diabetes adolescents Other
2019-08-19
EGAS00001003817 Functional analysis of GATA2 synonymous mutations Other
2019-08-20
EGAS00001003818 Lothian Birth Cohort 1921 whole genome sequencing study Other
2019-08-20
EGAS00001003819 Lothian Birth Cohort 1936 whole genome sequencing study Other
2019-08-20
EGAS00001003820 Molecular patterns of response and treatment failure after frontline venetoclax combinations in older patients with AML Other
2019-08-21
EGAS00001003821 Preservation of stemness in high-grade serous ovarian cancer organoids requires low Wnt environment Other
2019-08-21
EGAS00001003822 Epigenomics and Single-cell Sequencing Define a Developmental Hierarchy in Langerhans Cell Histiocytosis Other
2019-08-22
EGAS00001003823 Gene_epression_regulation_in_cytokine_induced_immune_cell_states Gene Regulation Study
2019-08-23
EGAS00001003826 Exome sequencing of Fibromyalgia patients Other
2019-08-24
EGAS00001003827 eccDNA in maternal plasma Other
2019-08-26
EGAS00001003828 Genomic landscape and PD-1 blockade in Natural-killer/T cell lymphoma Other
2019-08-26
EGAS00001003829 Clonal evolution in myelofibrosis during ruxolitinib therapy Exome Sequencing
2019-08-26
EGAS00001003830 Deep multi-region whole-genome sequencing reveals heterogeneity and gene-by-environment interactions in treatment-naive, metastatic lung cancer Other
2019-08-27
EGAS00001003831 Exome sequencing data for 40 cases of alopecia areata and vitiligo Other
2019-08-27
EGAS00001003832 Delineating intratumoural heterogeneity and neoantigen-directed immune escape in Esophageal Squamous Cell Carcinoma Other
2019-08-27
EGAS00001003834 Genomic Analysis of Primary Plasma Cell Leukemia reveals Complex Structural Alterations and High Risk Mutational Patterns Other
2019-08-27
EGAS00001003837 RNA-seq, WGS and WES of Hepatocellular carcinomas, enriched in fibrolamellar carcinomas Other
2019-08-28
EGAS00001003839 Whole exome sequencing CYLD cutaneous syndrome Other
2019-08-30
EGAS00001003840 Targeted sequencing CYLD cutaneous syndrome Other
2019-08-30
EGAS00001003841 RNA sequencing CYLD cutaneous syndrome Other
2019-08-30
EGAS00001003842 Osteosarcoma mate-pair and RNA-sequencing Other
2019-09-02
EGAS00001003843 C3 SNPs and outcome after lung transplantation Other
2019-09-04
EGAS00001003845 A single-cell atlas of human glioma Other
2019-09-05
EGAS00001003846 Deciphering Intratumoral Molecular Heterogeneity in Clear Cell Renal Cell Carcinoma with a Radiogenomics Platform Other
2019-09-05
EGAS00001003847 Longitudinal_profiling_of_the_immune_response_to_Plasmodium_vivax_in_naive_hosts_by_RNA_sequencing Transcriptome Analysis
2019-09-06
EGAS00001003848 The evolutionary steps from primary to metastatic prostate cancer are largely uncharted, and the ability to use DNA present in body fluids as correlates of aggregate metastatic status is under-examined. We reconstructed phylogenies in ten prostate cancer patients with fatal disease using deep targeted sequencing of the prostate, adjacent and distant organs, as well as plasma, serum, and cerebrospinal fluid at various time points. A total of 163 samples are studied. Other
2019-09-06
EGAS00001003849 Evaluation of protocols for rRNA depletion-based RNA sequencing of nanogram inputs of mammalian total RNA Transcriptome Analysis
2019-09-06
EGAS00001003850 Discovering genetic causes of optic atrophy syndromes through whole exome sequencing Other
2019-09-09
EGAS00001003852 Modeling glioblastoma invasion using human brain organoids and single-cell transcriptomics Other
2019-09-09
EGAS00001003853 Sequencing of an organoid biobank for childhood kidney cancers that captures disease and tissue heterogeneity. Other
2019-09-10
EGAS00001003856 Targeted sequencing of patients affected by familial or sporadic Alzheimer's disease Other
2019-09-10
EGAS00001003857 WES of melanoma tumors treated with combined immune checkpoint blockade Other
2019-09-10
EGAS00001003860 Single cell phenotypic profiling of 27 DLBCL cases reveals marked inter- and intra-tumoral heterogeneity Other
2019-09-12
EGAS00001003861 IDENTIFICATION AND TARGETED MANAGEMENT OF A PATIENT WITH A NEURODEGENERATIVE DISORDER CAUSED BY BIALLELIC MUTATIONS IN SLC5A6 Other
2019-09-13
EGAS00001003862 Transcriptome_analysis_of_LCM_samples_ Transcriptome Analysis
2019-09-13
EGAS00001003863 Evolution_of_the_cancer_epigenome_in_myeloproliferative_neoplasms_TGS Cancer Genomics
2019-09-13
EGAS00001003870 Comprehensive Genomic Characterization of Gene Therapy-Induced T-cell Acute Lymphoblastic Leukemia (H007) Other
2019-09-16
EGAS00001003872 VIKING Health Study - Shetland Other
2019-09-17
EGAS00001003875 SG10K_Pilot - Large-scale whole-genome sequencing of three diverse Asian populations in Singapore Other
2019-09-18
EGAS00001003876 Whole Genome Sequencing Reveals Potential Therapeutic Strategy for Monomorphic Epitheliotropic Intestinal T-cell Lymphoma Other
2019-09-20
EGAS00001003882 Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___GI___LYNCH___WGS Whole Genome Sequencing
2019-09-20
EGAS00001003883 Systematic comparative analysis of single-nucleotide variants detection methods from single-cell RNA sequencing data Other
2019-09-23
EGAS00001003886 Immunopeptidomics of colorectal cancer organoids reveals a sparse HLA class I neoantigen landscape and no increase in neoantigens with interferon or MEK-inhibitor treatment Cancer Genomics
2019-09-23
EGAS00001003887 Immuno-genomic landscape of osteosarcoma Other
2019-09-23
EGAS00001003888 RNAseq_of_Human_Organoid_Lines Cancer Genomics
2019-09-23
EGAS00001003889 Studying the single cell characteristics of pancreatic cancer Other
2019-09-24
EGAS00001003890 Oesophageal_Adenocarcinoma_Organoid_ATAC Cancer Genomics
2019-09-25
EGAS00001003892 Multimodal Genomic Features Predict Outcome of Immune Checkpoint Blockade in Non-small Cell Lung Cancer Other
2019-09-26
EGAS00001003893 Transcriptome sequencing of gingivo-buccal oral squamous cell carcinoma for integrative analysis: alterations in expression of genes attributable to methylation changes Other
2019-09-26
EGAS00001003895 Whole genome and whole transcriptome sequencing of patients diagnosed with angiosarcoma. Other
2019-09-27
EGAS00001003896 Epigenome wide DNA methylation assay of gingivo-buccal oral squamous cell carcinoma using single base resolution high throughput array Other
2019-09-27
EGAS00001003897 Single-cell T-cell receptor sequencing of intraepithelial gammadelta T-cells in celiac disease Other
2019-09-27
EGAS00001003899 Identification of hypermutation and defective mismatch repair in ctDNA from metastatic prostate cancer Other
2019-09-27
EGAS00001003901 Screening of 2.5 million SNPs in 142 samples from the western Mediterranean area Other
2019-09-29
EGAS00001003917 Human Biofluid RNA Atlas Project - raw data RNASeq
2019-09-30
EGAS00001003922 Meisal temporal lobe epilepsy sequencing study Other
2019-09-30
EGAS00001003923 WES of 2 human osteosarcoma and corresponding cell lines Other
2019-10-01
EGAS00001003928 Cistrome-partitioning reveals convergence of somatic mutations and risk-variants on master transcription regulators in primary prostate tumors Other
2019-10-02
EGAS00001003931 Pan-neuroblastoma analysis reveals age- and signature-associated driver alterations Other
2019-10-02
EGAS00001003932 Polymorphisms in the mitochondrial genome are associated with bullous pemphigoid in Germans Other
2019-10-03
EGAS00001003933 ImmunoAgeing_Colonies Other
2019-10-03
EGAS00001003934 Mutational signature in colorectal cancer induced by genotoxic pks+ E. coli Other
2019-10-04
EGAS00001003941 Germline MBD4 Mutations and Predisposition to Uveal Melanoma Other
2019-10-07
EGAS00001003942 Deep intronic homozygous variation in PSMC3 causes a syndromic neurosensory disorder combining deafness and cataract Other
2019-10-07
EGAS00001003944 Description and determinants of the faecal resistome and microbiome of farmers and slaughterhouse workers: a metagenome-wide cross-sectional study. Other
2019-10-08
EGAS00001003946 Natural Killer Cell Plasticity During IL-15-driven Homeostatic Proliferation Other
2019-10-08
EGAS00001003949 Molecular profiling of DLBCL patients treated in the HOVON84 trial Other
2019-10-10
EGAS00001003950 Characterization of HCV-specific CD4 T cells during DAA-Therapy Other
2019-10-10
EGAS00001003951 CRISPR-based adenine editors correct nonsense mutations in a cystic fibrosis organoid biobank. Whole Genome Sequencing
2019-10-10
EGAS00001003952 Targeted_sequencing_of_embryonic_variants___Warm_Autopsy Cancer Genomics
2019-10-10
EGAS00001003953 Glioblastoma epigenome profiling identifies SOX10 as a master regulator of molecular tumour subtype Other
2019-10-10
EGAS00001003955 Genomic landscape of signals of positive natural selection in North Eurasia Other
2019-10-14
EGAS00001003958 genome-wide cfDNA methylation analysis Other
2019-10-15
EGAS00001003962 Breast implant-associated anaplastic large cell lymphoma shallow whole genome sequencing for copy number analysis and Whole exome sequencing data. Other
2019-10-17
EGAS00001003963 Rapid identification of somatic genome rearrangements as personalized biomarkers for blood-based cancer monitoring Other
2019-10-17
EGAS00001003964 Partner-independent fusion gene detection by multiplexed CRISPR/Cas9 enrichment and long-read Nanopore sequencing Other
2019-10-17
EGAS00001003967 STRATAA_RNAseq Other
2019-10-18
EGAS00001003968 Intellectual Disability cases with parents (trios) or affected sibs (sibpairs) Other
2019-10-18
EGAS00001003970 Whole-exome sequencing of intravascular large B-Cell lymphoma Other
2019-10-18
EGAS00001003973 Direct Comparative Analysis of 10X Genomics Chromium and Smart-seq2 Other
2019-10-20
EGAS00001003974 A Unifying Paradigm for Transcriptional Heterogeneity and Squamous Features in Pancreatic Ductal Adenocarcinoma Other
2019-10-21
EGAS00001003975 Mutational landscape and patterns of clonal evolution in relapsed pediatric acute lymphoblastic leukemia Other
2019-10-22
EGAS00001003976 Phenotypic_characterisation_of_LRRN4CL_over_expression Transcriptome Analysis
2019-10-23
EGAS00001003979 Activation of IL7RA signalling in human B-lymphoid precursors induces pre-leukemia Cancer Genomics
2019-10-24
EGAS00001003980 Molecular Profiles of BRCA1-Associated Ovarian Cancer Treated by Platinum-Based Therapy Cancer Genomics
2019-10-25
EGAS00001003981 Sequencing data of multiple sarcoma samples for personalized medicine and endotype identification Other
2019-10-25
EGAS00001003982 Increased mutation accumulation during fetal development in Down syndrome Other
2019-10-28
EGAS00001003984 SCLC ctDNA sequencing Other
2019-10-28
EGAS00001003985 SCLC tumor sequencing Other
2019-10-28
EGAS00001003986 Investigation of relapse prediction in infants with MLL-rearranged Acute Lymphoblastic Leukemia Other
2019-10-28
EGAS00001003987 SCC ctDNA sequencing Other
2019-10-28
EGAS00001003988 SCC tumor sequencing Other
2019-10-28
EGAS00001003989 circulating-tumor DNA sequencing of healthy samples Other
2019-10-28
EGAS00001003991 MYO5B mutations in Pheochromocytoma/Paraganglioma promote cancer progression Other
2019-10-28
EGAS00001003992 Lindsey E. Jones et al. Patient-derived cells from recurrent tumors that model the evolution of IDH-mutant glioma. Neuro-Oncology Advances, 2020. We established robust, versatile, and well-characterized Patient Derived Cells (PDC) of an IDH1-mutant astrocytoma and an IDH1-mutant oligodendroglioma that represents defined evolutionary stages of chemotherapy-induced hypermutation. The PDCs retain tumor subtype defining features over time as well as classic hallmarks of cancer, including anchorage independent growth and cell immortality. The integrated phylogenies composed of PDCs,single-cell-derived PDCs, patient-derived xenografts, and corresponding spatiotemporal tumor tissue samples also provide new insight into the clonality, evolutionary pattern, and immense mutational load of hypermutated IDH mutant gliomas. Other
2019-10-29
EGAS00001003993 Peripheral clonal expansion of T cells (scRNA-seq) RNASeq
2019-10-29
EGAS00001003994 Peripheral clonal expansion of T cells (scTCR-seq) Other
2019-10-29
EGAS00001003996 A spatiotemporal organ-wide gene expression and cell atlas of the developing human heart Other
2019-10-29
EGAS00001003997 InsPIRE islets Other
2019-10-30
EGAS00001003999 Myeloma RNAseq RNASeq
2019-10-31
EGAS00001004000 Myeloma WGS Other
2019-10-31
EGAS00001004001 Tumor-specific expression of let-7i and miR-192 is associated with resistance to cisplatin-based chemoradiotherapy in patients with larynx and hypopharynx cancer Other
2019-11-01
EGAS00001004003 SSBP1 Other
2019-11-02
EGAS00001004006 Genomic and immune profiling of pre-invasive lung adenocarcinoma Other
2019-11-04
EGAS00001004007 Whole-genome sequencing of normal Singaporean volunteers Other
2019-11-04
EGAS00001004008 Single cell RNAseq of PBMC from bladder cancer patients Other
2019-11-04
EGAS00001004009 Spontaneous mutations in the single TTN gene represent high tumor mutation burden Other
2019-11-05
EGAS00001004012 Familial adult myoclonic epilepsy in Sri Lankan and Indian families Other
2019-11-06
EGAS00001004013 Whole genome, exome and transcriptome analysis to guide individualized cancer interpretation Other
2019-11-06
EGAS00001004014 Mapping the breast cancer metastatic cascade onto circulating tumour DNA using genetic and epigenetic clonal tracking Other
2019-11-06
EGAS00001004015 Reconstruction of complex rearrangement patterns causing the initiation of clear cell renal cell carcinoma. Other
2019-11-06
EGAS00001004016 Epigenomic data of HEMa_LP Other
2019-11-07
EGAS00001004018 A Protein Neddylation Inhibitor MLN4924 Suppresses Patient-Derived Glioblastoma Cells via Inhibition of ERK and AKT Signaling Other
2019-11-08
EGAS00001004019 Whole-genome bisulfite sequencing analysis of low-grade astrocytomas in the ICGC PedBrain Tumor Project Other
2019-11-08
EGAS00001004020 Uncovering tumor intrinsic and extrinsic factors that regulate hepatocellular carcinoma growth using patient derived xenograft assays Other
2019-11-08
EGAS00001004022 Berlin Neuroblastoma Dataset Cancer Genomics
2019-11-09
EGAS00001004023 Multi-regional tumour biopsies of a RET fusion patient Other
2019-11-11
EGAS00001004026 Whole exome sequencing from early stage non-small cell lung cancer patients at MDACC Other
2019-11-13
EGAS00001004027 Tumor intrinsic and extrinsic mechanisms of response and resistance to blinatumomab in relapsed/refractory acute lymphoblastic leukemia Other
2019-11-13
EGAS00001004028 Exome Sequencing of Spanish Patients with rare genetic diseases. Other
2019-11-14
EGAS00001004030 Single-cell analysis reveals fibroblast clusters linked to immunotherapy resistance in cancer Other
2019-11-15
EGAS00001004031 RNA-seq data from iCAF (sorted) and myCAF cluster 0 (spread) CAF-S1 fibroblasts maintained in culture Other
2019-11-15
EGAS00001004032 RNA-seq data from Non Small Cell Lung Cancer (NSCLC) samples Other
2019-11-15
EGAS00001004033 UCSF Pediatric Bithalamic Glioma Genome Project Other
2019-11-17
EGAS00001004034 GRIDSS, PURPLE, LINX: Unscrambling the tumor genome via integrated analysis of structural variation and copy number Other
2019-11-18
EGAS00001004035 Single Cell Sperm sequencing try 2 Other
2019-11-18
EGAS00001004036 Genomic insight into the origins and dispersal of the Brazilian Coastal Natives Population Genomics
2019-11-18
EGAS00001004042 Human Pancreatic Islet RNAseq - Lund Other
2019-11-19
EGAS00001004043 Immune-awakening revealed by peripheral T cell dynamics after one cycle of immunotherapy Other
2019-11-20
EGAS00001004044 GWAS data on human pancreatic islets from 191 donors - Lund Other
2019-11-20
EGAS00001004050 Neoantigen responses to Immunotherapy in Prostate Cancer Other
2019-11-21
EGAS00001004051 Oesophageal_Adenocarcinoma_Organoids_Iso_Seq Cancer Genomics
2019-11-21
EGAS00001004053 Cell type-specific transcriptomics of esophageal adenocarcinoma as a scalable alternative for single cell transcriptomics Other
2019-11-22
EGAS00001004055 Concurrent germline and somatic pathogenic BAP1 variants in a patient with metastatic bladder cancer Cancer Genomics
2019-11-25
EGAS00001004056 Phenotyping data on human pancreatic islets from 191 donors - Lund Other
2019-11-25
EGAS00001004059 Expression profiles and genetic makeup of metastases of a cancer of unknown primary. Cancer Genomics
2019-11-26
EGAS00001004063 Organoid cultures of early-onset colorectal cancers reveal distinct and rare genetic profiles Other
2019-11-27
EGAS00001004064 Heterogeneous metabolic signatures are linked to cancer cell differentiation in colorectal cancer Other
2019-11-27
EGAS00001004066 Bottleneck_Sequencing_Of_Human_Tissue__Wgs_ Cancer Genomics
2019-11-27
EGAS00001004069 HCA_Placenta_Adult_Vento_RNA Other
2019-11-27
EGAS00001004070 single-cell RNA-seq Case-Control study of children progressing to Type1 diabetes Other
2019-11-29
EGAS00001004071 RNA-seq study of longitudinal blood cell samples from children at risk of type 1 diabetes Other
2019-11-29
EGAS00001004074 Neoadjuvant combination PD-L1 plus CTLA-4 blockade in patients with cisplatin-ineligible operable urothelial carcinoma Other
2019-12-02
EGAS00001004075 The Jerusalem Perinatal Study (JPS) aimed to examine the developmental origins of cardiometabolic risk. Other
2019-12-03
EGAS00001004076 Molecular and Clonal Evolution in Recurrent Metastatic Gliosarcoma Other
2019-12-03
EGAS00001004077 Whole exome sequencing study for 8 pairs of primary NSCLCs and distant metastases Other
2019-12-03
EGAS00001004078 RNA sequencing study for 8 pairs of primary NSCLCs and distant metastases Other
2019-12-03
EGAS00001004079 DNA methylation array study for 7 pairs of primary NSCLCs and distant metastases Other
2019-12-03
EGAS00001004080 End structure of DNA in plasma: detection, characterizationand diagnostic applications Other
2019-12-04
EGAS00001004081 RNA sequencing of CD8 T cells from melanoma patients prior to and during checkpoint immunotherapy and untreated healthy controls Other
2019-12-04
EGAS00001004082 Single cell RNA-seq mapping of nasal and tracheobronchial airways in human healthy volunteers Other
2019-12-04
EGAS00001004084 Whole Exome Sequencing of Spanish Patients diagnosed with rare ophtalmogenetic disorders: Macular Dystrophy, Retinitis Pigmentosa and Leber's congenital amaurosis. Exome Sequencing
2019-12-04
EGAS00001004085 Single-cell RNA sequencing of 22 Hodgkin lymphoma tumors and 5 reactive lymph nodes Other
2019-12-04
EGAS00001004086 Whole exome sequencing of advanced gastric cancer Other
2019-12-05
EGAS00001004087 Multiple Sclerosis risk variants regulate gene expression in innate and adaptive immune cells Other
2019-12-05
EGAS00001004088 Rapid response of APC/TP53/KRAS mutated stage IV colorectal cancer under FOLFIRI + Bevacizumab detected by liquid biopsy: a case report Other
2019-12-05
EGAS00001004089 HCA_Adrenal_Foetal_WSSS_RNA_SB Transcriptome Analysis
2019-12-05
EGAS00001004090 HNSCC RNA-seq RNASeq
2019-12-05
EGAS00001004091 HNSCC copy number alterations Whole Genome Sequencing
2019-12-05
EGAS00001004092 Mitochondrial DNA sequencing in samples of Huntington’s disease patients Other
2019-12-05
EGAS00001004093 Comparison of structural variations from 10X Genomics linked-reads and conventional Illumina short-reads sequencing Other
2019-12-06
EGAS00001004097 Evolutionary Origins of Recurrent Pancreatic Cancer Other
2019-12-07
EGAS00001004102 SDH_deficient_renal_tumours___WGS_ Other
2019-12-09
EGAS00001004103 SDH_deficient_renal_tumours___RNA_ Other
2019-12-09
EGAS00001004106 Comprehensive pharmacogenomic characterization of gastric cancer Other
2019-12-11
EGAS00001004107 Single cell RNA seq of the developing human embryo brain Other
2019-12-11
EGAS00001004108 54 metastatic colorectal cancer patients from Schleswig-Holstein in North Germany Other
2019-12-11
EGAS00001004110 Exon4-mutations in KRAS Affect MEK-ERK and Pi3K-AKT Signaling in Multiple Myeloma Other
2019-12-12
EGAS00001004111 Y chromosome variability in Polish population Other
2019-12-12
EGAS00001004112 Reference Exome Data for a Northern Brazilian population Other
2019-12-13
EGAS00001004113 Lenalidomide Resistance in del(5q) Myelodysplastic Syndrome Follows Loss of RUNX1/TP53-mediated Megakaryocytic Differentiation Other
2019-12-13
EGAS00001004114 White blood cell and cell-free DNA analyses for detection of residual disease in gastric cancer Other
2019-12-15
EGAS00001004115 Quality of Whole Genome Sequencing from Blood versus Saliva Derived DNA in Cardiac Patients Whole Genome Sequencing
2019-12-16
EGAS00001004116 CD8+ T-cell exhaustion induced by leukemic cells drives progression in Chronic Lymphocytic Leukemia Other
2019-12-16
EGAS00001004117 Genomic landscape of inflammatory breast cancer by whole-genome sequencing Other
2019-12-16
EGAS00001004118 Imaging metabolic heterogeneity in breast cancer using hyperpolarized 13C-MRI Other
2019-12-16
EGAS00001004122 Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___GI___MAP___WGS Cancer Genomics
2019-12-17
EGAS00001004123 Benchmarking of ProSolo, a new probabilistic single nucleotide variant caller for single cell DNA sequencing data. This study provides the whole exome sequencing dataset used in this assessment. Other
2019-12-18
EGAS00001004124 Genomic_characterisation_of_MGUS__ Cancer Genomics
2019-12-18
EGAS00001004126 Germline elongator mutations in sonic hedgehog medulloblastoma Other
2019-12-19
EGAS00001004127 RNASeq for BMI GL study RNASeq
2019-12-23
EGAS00001004135 Comparison of 133/144bp dominant phenotype vs 166bp dominant phenotype. Other
2020-01-07
EGAS00001004136 Phased whole genome sequencing of 10 melanoma samples Other
2020-01-07
EGAS00001004139 Amplicon based NGS of human CD4 and CD8 T cells Other
2020-01-08
EGAS00001004145 Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis Other
2020-01-09
EGAS00001004147 Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells Gene Regulation Study
2020-01-10
EGAS00001004151 Cancer immune control needs senescence induction by Stat1 dependent cell cycle regulator pathways in tumours Other
2020-01-10
EGAS00001004152 Transcriptomic signatures of CD4+ T cells from visceral leishmaniasis (VL) patients Other
2020-01-13
EGAS00001004153 The miR-185/PAK6 Axis Predicts Therapy Response and Regulates Survival of Drug-Resistant Leukemic Stem Cells in Chronic Myeloid Leukemia Other
2020-01-13
EGAS00001004156 FAM50A_Disruption_in_TOV21G_Cells___RNAseq Cancer Genomics
2020-01-15
EGAS00001004157 Metastatic Adult Pancreatoblastoma: Multimodal Treatment and Molecular Characterization of a Very Rare Disease (NCT MASTER) Other
2020-01-15
EGAS00001004160 Neoadjuvant immunotherapy leads to pathological responses in MMR proficient and MMR deficient early stage colon cancers Other
2020-01-17
EGAS00001004165 Genomic and epigenomic insights into the origin, pathogenesis and clinical behavior of mantle cell lymphoma subtypes Other
2020-01-19
EGAS00001004168 High-resolution analyses of human sperm dynamic methylome reveals thousands of novel age-related epigenetic alterations Other
2020-01-20
EGAS00001004169 Chromatin run-on and RNA sequencing of fibrolamellar carcinoma Other
2020-01-20
EGAS00001004175 Whole-exome sequencing of the transposition of the great arteries Other
2020-01-21
EGAS00001004176 Two monogenic disorders masquerading as one: Severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss Exome Sequencing
2020-01-22
EGAS00001004177 The role of the mammalian SWI/SNF chromatin remodeling complex in neuroendocrine prostate cancer Other
2020-01-22
EGAS00001004181 JAK and STAT alterations in CD30 positive LPD Cancer Genomics
2020-01-22
EGAS00001004182 Targeted sequencing of breast cancers with germline BRCA1/2 mutations Other
2020-01-22
EGAS00001004186 Prostate Cancer mitochondrial DNA heteroplasmies and mitochondrial gene expression Cancer Genomics
2020-01-25
EGAS00001004187 Vento_Placental_Cell_Atlas Other
2020-01-27
EGAS00001004189 Integrative molecular analysis of pediatric Anaplastic large cell lymphoma reveals subtypes with distinct immune suppression signatures. Other
2020-01-27
EGAS00001004192 Transcriptomic response of miRNAs of monocytes to bacterial and viral stimuli assessed by RNA-seq in Africans and Europeans Other
2020-01-29
EGAS00001004193 HSC_population_dynamics___KX007_samples Cancer Genomics
2020-01-29
EGAS00001004194 cfRRBS on cfDNA from pediatric cancer Other
2020-01-30
EGAS00001004196 pancreatic ductal adenocarcinoma exomes in study: Pro-immunogenic Impact of MEK inhibition combined with an anti-CD40 immunostimulatory antibody Other
2020-01-31
EGAS00001004197 Immuno-genomic landscape of osteosarcoma Other
2020-01-31
EGAS00001004199 Gene expression in brain (Schizophrenia) study Other
2020-02-03
EGAS00001004200 High coverage sequencing of a single sample can account for the problem of intratumor heterogeneity Exome Sequencing
2020-02-03
EGAS00001004201 StemNet - in vitro differentiation of human hepatocytes Other
2020-02-03
EGAS00001004203 Genetics and transcriptomics of human acute erythroid leukemia Cancer Genomics
2020-02-05
EGAS00001004204 Whole exome sequencing in familial Multiple Sclerosis Other
2020-02-05
EGAS00001004207 Sex-biased patterns shaped the genetic history of Roma Other
2020-02-06
EGAS00001004208 Pancreatic tropism of metastatic renal cell carcinoma Other
2020-02-06
EGAS00001004209 Native American gene flow into Polynesia predating Easter Island settlement Other
2020-02-07
EGAS00001004210 HCA_Female_Reporductive_Adult_WSSS_RNA Other
2020-02-07
EGAS00001004211 Association of DNA-methylation profiles with immune responses in breast cancer patients Epigenetics
2020-02-07
EGAS00001004212 The application of RNA sequencing for the diagnosis and genomic classification of pediatric acute lymphoblastic leukemia Other
2020-02-09
EGAS00001004213 Real-time response profiling through serial plasma analyses during FOLFOX treatment in patients with colorectal cancer Other
2020-02-10
EGAS00001004214 Analysis of exonic somatic variants in light-chain amyloidosis (ALA) and ALA concomitant with multiple myeloma Other
2020-02-10
EGAS00001004216 Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome Other
2020-02-10
EGAS00001004218 HDAC3 mediates the inflammatory response and LPS tolerance in human monocytes and macrophages RNASeq
2020-02-12
EGAS00001004220 KDM4A regulates the maternal-to-zygotic transition by protecting broad H3K4me3 domains from H3K9me3 invasion in oocytes Transcriptome Analysis
2020-02-12
EGAS00001004221 Whole-genome DNA methylation profiling of CD14+ monocytes reveals disease status and activity differences in Crohn’s disease patients Other
2020-02-12
EGAS00001004224 CYPTAM - PacBio SMRT sequencing Other
2020-02-12
EGAS00001004228 Heterogeneous Genomic Evolution and Immune Microenvironments in Metastatic Lung Cancer Other
2020-02-14
EGAS00001004229 NanoSring of PBMC from bladder cancer and RCC patients Other
2020-02-14
EGAS00001004230 Single Cell RNAseq of blood and tumor from renal cancer patients Other
2020-02-14
EGAS00001004231 Whole exome sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer Exome Sequencing
2020-02-16
EGAS00001004232 Whole transcriptome sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer Other
2020-02-16
EGAS00001004233 Single-cell RNA sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer Other
2020-02-16
EGAS00001004235 Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes Other
2020-02-18
EGAS00001004237 The_Little_Princess_Knowledge_Bank_ Cancer Genomics
2020-02-18
EGAS00001004238 iNeuron_RNAseq Other
2020-02-18
EGAS00001004239 : Centromeric cohesion failure invokes a conserved choreography of chromosomal mis-segregations in pancreatic neuroendocrine tumours Cancer Genomics
2020-02-18
EGAS00001004241 Spinocerebellar ataxia type 3 RNA-sequencing study Other
2020-02-19
EGAS00001004242 Pediatric Low-Grade Glioma RNA and Targeted Sequencing Other
2020-02-19
EGAS00001004243 THE GENOMIC LANDSCAPE OF ACTINIC KERATOSIS Other
2020-02-19
EGAS00001004248 Whole-exome sequencing of ovarian clear cell carcinoma in clinical outliers Other
2020-02-21
EGAS00001004249 Adult granulosa cell tumor WGS data cohort with corresponding reference germline WGS data Other
2020-02-21
EGAS00001004250 The landscape of chromothripsis across adult cancer types Other
2020-02-21
EGAS00001004255 Single cell RNA-seq profiling of CD8 T cells from elder adults Other
2020-02-24
EGAS00001004266 Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma Other
2020-02-27
EGAS00001004267 Resequencing (MIPS) of candidate genes for Keratoconus (2020) Other
2020-02-27
EGAS00001004268 Bone metastatic biopsies of breast cancer patients progressing on endocrine therapies. Cancer Genomics
2020-02-28
EGAS00001004270 CHD8 RNAseq RNASeq
2020-02-28
EGAS00001004271 Genome-wide study of the effect of blood collection tubes on the cell-free DNA methylome Other
2020-02-28
EGAS00001004272 Genetic characterization of a Unique Neuroendocrine Transdifferentiation Prostate Circulating Tumor Cell - Derived eXplant (CDX) Model Cancer Genomics
2020-02-28
EGAS00001004273 RUNX1 mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML Other
2020-02-29
EGAS00001004274 Mutation signatures in melanocytic nevi reveal characteristics of defective DNA repair Other
2020-03-02
EGAS00001004275 Multiplexed quantification of four neuroblastoma DNA targets in a single droplet digital PCR reaction Other
2020-03-02
EGAS00001004276 Longitudinal therapy monitoring of ALK-positive non-small cell lung cancer (copy number, cell-free DNA) Other
2020-03-02
EGAS00001004277 Germline SDHB-inactivating mutation in gastric spindle cell sarcoma (HIPO-021) Other
2020-03-02
EGAS00001004280 ImmunoAgeing_Colonies_WGS Other
2020-03-03
EGAS00001004281 Spatial_transcriptome_analysis_of_Paediatric_Thymus Other
2020-03-03
EGAS00001004282 Successful BRAF/MEK-inhibition in a young patient with BRAF V600E-mutated extrapancreatic acinar cell carcinoma (HIPO-021) Other
2020-03-03
EGAS00001004283 Ensemble learning for classifying single-cell data and projection across reference atlases Other
2020-03-03
EGAS00001004284 The impact of urbanization and diet on innate immune responses in healthy Tanzanians RNASeq
2020-03-03
EGAS00001004285 The double-hit signature identifies double-hit diffuse large B-cell lymphoma with genetic events cryptic to FISH Other
2020-03-03
EGAS00001004286 Total RNAseq in the sporadic ALS and healthy control motor cortex Other
2020-03-04
EGAS00001004287 Roma Sequencing Study Other
2020-03-04
EGAS00001004288 Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma Exome Sequencing
2020-03-04
EGAS00001004289 Coding and non-coding drivers of mantle cell lymphoma identified through exome and genome sequencing Other
2020-03-04
EGAS00001004290 Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell RCC -- CA209-009 Other
2020-03-05
EGAS00001004291 Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell RCC -- CA209-010 Other
2020-03-05
EGAS00001004292 Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell RCC-- CA209-025 Other
2020-03-05
EGAS00001004293 MethCORR: DNA Methylation-based Characterization, Classification and Prognostication of Colorectal Cancer using Archival Formalin-fixed, Paraffin-embedded Tissue Other
2020-03-05
EGAS00001004296 Molecular profiling of metastatic uveal melanoma Other
2020-03-05
EGAS00001004298 IgCaller Other
2020-03-09
EGAS00001004301 H3.3G34R/V-transformed interneuron progenitors co-opt PDGFRA for gliomagenesis Other
2020-03-09
EGAS00001004303 Egyptref: An integrated personal and population-based Egyptian genome reference Other
2020-03-10
EGAS00001004311 Healthy_ageing_thymus Other
2020-03-12
EGAS00001004312 PFA ependymoma cancer study Other
2020-03-14
EGAS00001004314 Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma (arrays set) Other
2020-03-19
EGAS00001004315 Enhancer-gene rewiring in the pathogenesis of Quebec Platelet Disorder Epigenetics
2020-03-19
EGAS00001004316 Hereditary Cancer Diagnostics with I2HCP gene panel Other
2020-03-20
EGAS00001004319 Long-read trio sequencing of unsolved patients with intellectual disability Other
2020-03-24
EGAS00001004320 Multiregion Whole-Exome Sequencing Uncovers the Genetic Evolution and Mutational Heterogeneity of Early-Stage Metastatic Melanoma. Cancer Genomics
2020-03-24
EGAS00001004322 Rare_renal_tumours_WGS_ Other
2020-03-25
EGAS00001004323 Rare_renal_tumours_RNA_ Other
2020-03-25
EGAS00001004325 Atypical 3q26/MECOM rearrangements genocopy inv(3)/t(3;3) in acute myeloid leukemia Other
2020-03-26
EGAS00001004326 Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurological disorders Other
2020-03-26
EGAS00001004327 METABRIC: Data from Batra et al (2021); DNA methylation landscapes of 1538 breast cancers reveal a replication-linked clock, epigenomic instability and cis-regulation Other
2020-03-27
EGAS00001004328 Activating AKT1 and PIK3CA mutations in metastatic castration-resistant prostate cancer Cancer Genomics
2020-03-27
EGAS00001004329 Genomic_landscape_of_liver_cirrhosis Other
2020-03-29
EGAS00001004332 Whole-genome and transcriptome sequencing of primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma Other
2020-04-03
EGAS00001004335 Dissecting intratumor heterogeneity of nodal B cell lymphoma on the transcriptional, genetic, and drug response level Other
2020-04-06
EGAS00001004338 Umbrella Study of MASTER/H021 data (not to be released, pool) Cancer Genomics
2020-04-06
EGAS00001004340 Persistent STAG2 mutation in recurrent pediatric glioblastoma Other
2020-04-14
EGAS00001004341 Comprehensive molecular characterization of brainstem glioma Other
2020-04-14
EGAS00001004342 Plasma DNA profile in DNASE1L3 deficiency Other
2020-04-15
EGAS00001004343 Molecular determinants of response to PD-L1 blockade across tumor types Other
2020-04-15
EGAS00001004344 A molecular cell atlas of the human lung from single cell RNA sequencing Other
2020-04-15
EGAS00001004345 Multi-omics profiling of paired primary and recurrent glioblastoma patient tissues Other
2020-04-16
EGAS00001004346 Whole genome bisulfite sequencing on 10 multiple myeloma cases Other
2020-04-16
EGAS00001004347 RNAseq on 20 samples of multiple myeloma patients and 3 normal plasma cells. Other
2020-04-16
EGAS00001004348 Enhanced reduced representation bisulfite sequencing (eRRBS) on 45 multiple myeloma samples and 3 normal plasma cell Other
2020-04-16
EGAS00001004349 Alternative lengthening of telomeres in childhood neuroblastoma from genome to proteome Other
2020-04-16
EGAS00001004352 Epigenomic profile of diverse cancer Other
2020-04-17
EGAS00001004353 Molecular subsets in renal cancer determine outcome to checkpoint and angiogenesis blockade Other
2020-04-17
EGAS00001004355 Cell-free DNA fragmentation patterns and personalized sequencing reveal circulating tumor DNA in urine and plasma of glioma patients Other
2020-04-20
EGAS00001004356 Phylogenetic reconstruction of breast cancer Other
2020-04-20
EGAS00001004357 Whole-exome sequencing of extranodal NK/T cell lymphoma Other
2020-04-20
EGAS00001004358 RNA-sequencing of Non-muscle Invasive Bladder cancer (NMIBC) Other
2020-04-20
EGAS00001004359 Sequencing of an adolescent patient with germline RET mutant alveolar rhabdomyosarcoma Other
2020-04-20
EGAS00001004361 TP53 variant detection analysis in high grade serous epithelial ovarian cancer Other
2020-04-21
EGAS00001004362 Genetic diversity and continuity of the population of the UAE Other
2020-04-21
EGAS00001004363 Comprehensive Genomic Characterization of Refractory Multiple Myeloma Reveals a Complex Mutational and Structural Landscape Associated with Drug Resistance (H067) Other
2020-04-21
EGAS00001004364 Whole-genome sequencing of rare disease patients in a national healthcare system Other
2020-04-21
EGAS00001004365 Candidate Gene Case Control Study of Human African Trypanosomiasis in the Democratic Republic of Congo Other
2020-04-21
EGAS00001004366 Molecular stratification of endometrioid ovarian carcinoma predicts clinical outcome Other
2020-04-21
EGAS00001004367 Skeletal muscle transcriptomic comparison between long-term trained and untrained men and women Other
2020-04-22
EGAS00001004369 scRNA-seq data of BALF and blood cells from COPD and control Other
2020-04-22
EGAS00001004370 Epigenetic analyses of methylation and nucleosome occupancy in cell-free DNA (cfNOMe) Other
2020-04-22
EGAS00001004371 Whole exome sequencing identifies clinically relevant mutational signatures in resected hepatocellular carcinoma Other
2020-04-22
EGAS00001004373 Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis Other
2020-04-23
EGAS00001004374 Single cell characterization of arrested B-lymphoid differentiation and leukemic cell states in ETV6-RUNX1-positive pediatric leukemia RNASeq
2020-04-23
EGAS00001004375 RNA-seq of human embryonic heart, lung, and cerebellum Other
2020-04-23
EGAS00001004376 OSCC WES + WGS Boot et al. 2020 Cancer Genomics
2020-04-24
EGAS00001004379 Whole genome sequencing of glioblastoma reveals enrichment of non-coding constraint mutations in known and novel genes Other
2020-04-26
EGAS00001004380 Accurate mapping of mitochondrial DNA deletions and duplications using deep sequencing Other
2020-04-27
EGAS00001004381 scRNA-seq of HSPC treated with gemcitabine and carbplatin Other
2020-04-27
EGAS00001004383 Matching of actionable mutations with therapies in cancer patients: comparison of three commercial decision support platforms Other
2020-04-28
EGAS00001004386 Bulk RNAseq gene expression of baseline tumors from metastatic urothelial bladder cancer patients (IMvigor210) and metastatic renal cell carcinoma (IMmotion150) Other
2020-04-28
EGAS00001004388 Neuroblastoma and adrenal gland single-cell study Other
2020-04-29
EGAS00001004390 Subtype specific studies of breast cancer progression. Milan cohort. Other
2020-04-30
EGAS00001004391 Paediatric_and_adult_nasal_RNAseq___COVID19 Transcriptome Analysis
2020-04-30
EGAS00001004392 Genomic study of an AT-AML Other
2020-04-30
EGAS00001004394 Genome sequencing of oesophagus atresia families Other
2020-04-30
EGAS00001004395 glioblastoma and glioblastoma stem cells (GSCs), RNA-seq and WGS Other
2020-04-30
EGAS00001004396 Detailed molecular and immune marker profiling of archival prostate cancer samples Cancer Genomics
2020-04-30
EGAS00001004397 GBM stem cell lines and PRMT5 inhibitor Cancer Genomics
2020-04-30
EGAS00001004401 H3Africa - Respiratory Microbiota of African Children Other
2020-05-05
EGAS00001004402 Transcriptomic analysis of Acute Myeloid Leukemia stem cells Other
2020-05-05
EGAS00001004404 Accelerated single cell seeding in relapsed multiple myeloma Cancer Genomics
2020-05-05
EGAS00001004405 Homologous recombination DNA repair deficiency and PARP inhibition activity in primary triple negative breast cancer Other
2020-05-06
EGAS00001004406 Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring Other
2020-05-06
EGAS00001004407 Chemotherapy induces canalization of cell state in childhood B-cell precursor acute lymphoblastic leukemia Other
2020-05-07
EGAS00001004408 Search for genetic variants influencing gestational weight gain in type 1 diabetes patients by genome wide association method Other
2020-05-08
EGAS00001004409 Plasma DNA profile in DNASE1L3 deficiency-Mouse AAV samples Other
2020-05-08
EGAS00001004410 Scottish High Grade Serous Ovarian Cancer Other
2020-05-08
EGAS00001004412 Potent neutralizing antibodies against SARS-CoV-2 Other
2020-05-09
EGAS00001004413 Personalised Mapping of Tumour Development in Synchronous Colorectal Cancer Patients Other
2020-05-11
EGAS00001004415 WES Other
2020-05-11
EGAS00001004416 expression Other
2020-05-11
EGAS00001004418 STM4 - Mouliere et al, 2018. Enhanced detection of circulating tumor DNA by fragment size analysis Cancer Genomics
2020-05-11
EGAS00001004419 SARS‐CoV‐2 receptor ACE2 and TMPRSS2 are primarily expressed in bronchial transient secretory cells Other
2020-05-12
EGAS00001004420 Genome-wide associations of human gut microbiota variation and implications for causal inference analyses Other
2020-05-12
EGAS00001004422 Single-cell RNA-sequencing reveals that glioblastoma recapitulates a normal neurodevetlopmental hierarchy Other
2020-05-13
EGAS00001004424 RA-Map, A multi-omic survey of whole blood and subsets in early rheumatoid arthritis and vaccine study controls Other
2020-05-13
EGAS00001004428 Performance assessment of Total RNA sequencing of human biofluids and extracellular vesicles RNASeq
2020-05-14
EGAS00001004429 The genomic landscape of primary cutaneous anaplastic large cell lymphoma (pcALCL) Other
2020-05-15
EGAS00001004430 Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma Cancer Genomics
2020-05-15
EGAS00001004431 Dual-mTOR inhibitor Rapalink-1 reduces prostate cancer patient-derived xenograft growth and alters tumor heterogeneity Other
2020-05-16
EGAS00001004434 The Egyptian Collaborative Cardiac Genomics (ECCO-GEN) Project: Defining a Healthy Volunteer Cohort Other
2020-05-19
EGAS00001004435 DO NOT USE - Whole genome sequencing of SI-NETs from five patients Other
2020-05-19
EGAS00001004436 Highlighted samples from the BCH CRDC Other
2020-05-19
EGAS00001004437 Deep sequencing of the gut microbiome from 946 healthy donors of the Milieu Intérieur cohort Other
2020-05-20
EGAS00001004438 Immunogenomics of colorectal cancer response to immune checkpoint blockade Other
2020-05-20
EGAS00001004439 Patient-derived organoids as a novel tool to study cervical cancer Other
2020-05-21
EGAS00001004440 Single-cell DNA amplicon sequencing reveals clonal heterogeneity and evolution in T-cell acute lymphoblastic leukemia Other
2020-05-21
EGAS00001004443 Single-cell analysis for metastatic gastric adenocarcinoma Other
2020-05-21
EGAS00001004444 Immunogenomic landscape of hematological malignancies Other
2020-05-21
EGAS00001004445 Clinical efficacy and biomarker analysis of neoadjuvant atezolizumab in operable urothelial carcinoma in the ABACUS trial Other
2020-05-22
EGAS00001004446 ctDNA monitoring using patient-specific sequencing and integration of variant reads - Breast cohort Other
2020-05-22
EGAS00001004447 ctDNA monitoring using patient-specific sequencing and integration of variant reads - Lung cohort Other
2020-05-22
EGAS00001004448 Clonal fitness inferred from timeseries modeling of single cell cancer genomes Other
2020-05-22
EGAS00001004449 Single cell sequencing in CNS autoimmune disease RNASeq
2020-05-23
EGAS00001004451 Single cell RNAseq of PBMC from RCC patients Other
2020-05-24
EGAS00001004452 FOXM1 is a biomarker of resistance to PI3Kα inhibition in ER+ breast cancer that is detectable using metabolic imaging (RNA-seq data) Other
2020-05-24
EGAS00001004454 A molecular signature for IL-10-producing Th1 cells in protozoan parasitic diseases Other
2020-05-26
EGAS00001004455 CRISPR/Cas9-mediated genome editing of Schistosoma mansoni acetylcholinesterase Other
2020-05-26
EGAS00001004456 Comparative analysis of somatic variant calling on matched FF and FFPE WGS samples Other
2020-05-26
EGAS00001004458 Single cell RNAseq of PBMC from bladder cancer patients Other
2020-05-27
EGAS00001004459 Khoe-San genomes reveal unique variation and confirm deepest population divergence in Homo sapiens Other
2020-05-28
EGAS00001004460 Modulation of macrophage inflammatory function through selective inhibition of the epigenetic reader protein SP140 Other
2020-05-29
EGAS00001004461 Whole-exome sequencing and microRNA profiling predicted relapse risk of stage I lung adenocarcinomas Other
2020-05-30
EGAS00001004462 Mutational_burden_in_human_hair_follicles Cancer Genomics
2020-06-01
EGAS00001004463 Immunoreactive_p53_areas_in_human_skin_2 Cancer Genomics
2020-06-01
EGAS00001004464 _WGS__Somatic_mutation_in_skin_epidermis__SMS_ Cancer Genomics
2020-06-01
EGAS00001004465 WGS_skin_punches Cancer Genomics
2020-06-01
EGAS00001004466 Single cell RNA sequencing of normal endometrial derived organoids uncovers novel cell type markers for prognostication Other
2020-06-01
EGAS00001004467 Initial whole genome sequencing of plasma cell neoplasms in First Responders exposed to the World Trade Center attack of September 11, 2001 Other
2020-06-01
EGAS00001004468 A Single-Cell Atlas of the Multicellular Ecosystem of Primary and Metastatic Hepatocellular Carcinoma Other
2020-06-02
EGAS00001004470 Defective mitophagy and enhanced oxidative stress dictate regulatory T cell impairment in autoimmunity Other
2020-06-02
EGAS00001004472 Collection of Genotypic and Ethnographic Information from Individuals of South African Ethnic Groups Other
2020-06-03
EGAS00001004473 Evolutionary analysis of pancreatic neoplastic cysts through whole-exome and targeted sequencing Other
2020-06-03
EGAS00001004476 RNA sequencing of subchondral bone from patients that underwent a joint replacement surgery due to osteoarthritis. RNASeq
2020-06-04
EGAS00001004477 Versatile workflow for cell-type resolved transcriptional and epigenetic profiles from cryopreserved human lung Other
2020-06-04
EGAS00001004478 Identifying the role of ID3 in DNA repair and maintenance of genome integrity Other
2020-06-09
EGAS00001004479 Profiling the unique protective properties of intracranial arterial endothelial cells Other
2020-06-09
EGAS00001004480 The gut microbiota in prediabetes and diabetes: a population-based cross-sectional study Other
2020-06-10
EGAS00001004481 Single-cell analysis of airway samples identifies immune cell activation correlating with COVID-19 disease severity Other
2020-06-10
EGAS00001004482 Mutational Landscape of Grey Zone Lymphoma Other
2020-06-10
EGAS00001004484 Single-cell sequencing of gammadelta and CD8+ alphabeta TCR sequences from blood and gut in coeliac disease Other
2020-06-11
EGAS00001004485 EORTC RP1335 SPECTA Lung cancer data Other
2020-06-12
EGAS00001004486 Whole exome sequencing of long-term, never relapse exceptional responders of trastuzumab-treated HER2+ metastatic breast cancer Other
2020-06-12
EGAS00001004489 Autoimmunity_and_immunodeficiency_COVID19 Other
2020-06-16
EGAS00001004490 HSC_population_dynamics___KX008_samples Whole Genome Sequencing
2020-06-16
EGAS00001004491 A higher ctDNA fraction decreases survival in regorafenib-treated metastatic colorectal cancer patients Other
2020-06-16
EGAS00001004492 Fine-Scale Genomic Analyses Of Admixed Individuals Reveal Unrecognized Genetic Ancestry Components In Argentina Other
2020-06-17
EGAS00001004494 Cabozantinib Response in ETV6-NTRK3 G623R Positive Carcinoma HIPO-021 Other
2020-06-18
EGAS00001004495 Targets of MEK inhibition in DIPG Other
2020-06-19
EGAS00001004497 Molecular analysis of CRC in patients with Primary Sclerosing Cholangitis (PSC) and Inflammatory Bowel Disease (IBD) Cancer Genomics
2020-06-19
EGAS00001004499 Uterine leiomyoma: DNA methylation, chromatin activity and gene expression Other
2020-06-22
EGAS00001004502 Swarm Learning to identify COVID-19, tuberculosis and leukemia patients based on blood transcriptomes Transcriptome Analysis
2020-06-22
EGAS00001004503 Peripheral immunoprofiling of stratifies COVID-19 patients based on disease-specific neutrophil signatures Other
2020-06-22
EGAS00001004504 Human T-bet governs innate and innate-like adaptive IFN-g immunity against mycobacteria. Other
2020-06-23
EGAS00001004505 RNA-seq data from 121 tumor samples with muscle invasive bladder cancer. Other
2020-06-24
EGAS00001004507 WES data from 165 tumor/germline samples with muscle invasive bladder cancer. Other
2020-06-25
EGAS00001004508 Three-dimensional human alveolar stem cell culture models reveal infection response to SARS-CoV-2 Other
2020-06-25
EGAS00001004510 Characterization of four subtypes in morphologically normal tissue excised proximal and distal to breast cancer Other
2020-06-26
EGAS00001004511 Mutator phenotype and specific mutational signature explain an increased risk of hematological malignancies in patients with Xeroderma Pigmentosum Other
2020-06-26
EGAS00001004512 A reference map of potential determinants for the human serum metabolome Other
2020-06-28
EGAS00001004515 EPIC arrays data for chemotherapy response project Other
2020-06-29
EGAS00001004516 Transcriptomic profiling of lymphedema Other
2020-06-29
EGAS00001004517 Degradation of Cyclin K/CDK12 is a druggable vulnerability of colorectal cancer (H012) Cancer Genomics
2020-06-29
EGAS00001004518 The Molecular Landscape of Asian Breast Cancers Reveals Clinically Relevant Population-Specific Differences Other
2020-06-30
EGAS00001004519 SNP arrays for chemotherapy response project Other
2020-06-30
EGAS00001004521 Preoperative ipilimumab plus nivolumab in locoregionally advanced urothelial cancer (NABUCCO Cohorts 1 and 2) Other
2020-07-01
EGAS00001004523 An epigenetic single-cell atlas of IDH-mutant glioma reveals the role of ATRX in shaping tumor composition Other
2020-07-01
EGAS00001004524 Changes in alternative splicing and associated neo-antigens due to therapy Other
2020-07-01
EGAS00001004525 Multiscale heterogeneity in gastric adenocarcinoma evolution is an obstacle to precision medicine Cancer Genomics
2020-07-01
EGAS00001004527 WES sequencing of malignant peripheral nerve sheath tumours Other
2020-07-02
EGAS00001004528 RNA seq of MPNST tumour samples Other
2020-07-02
EGAS00001004532 RNA Sequencing of paediatric patients with B lymphoblastic leukemia Other
2020-07-06
EGAS00001004533 RNA-Sequencing and Somatic Mutation Status of Adrenocortical Tumors: Novel Pathogenetic Insights Other
2020-07-06
EGAS00001004534 Transcriptomic analysis of the Phase 3 COMPARZ clinical trial Other
2020-07-06
EGAS00001004535 Whole genome sequencing for novel neuromuscular disease gene discovery Other
2020-07-07
EGAS00001004536 Multiomic profiling of early-passage melanoma cell lines. Other
2020-07-07
EGAS00001004538 Memory-like HCV-specific CD8+ T cells retain a chronic scar after cure of chronic HCV infection Other
2020-07-07
EGAS00001004539 Clinical relevance of somatic copy-number alterations in plasma circulating tumor DNA from advanced EGFR-mutated NSCLC patients treated with osimertinib Other
2020-07-07
EGAS00001004540 Whole Genome Sequencing of 317 individuals from the Pacific region Other
2020-07-08
EGAS00001004541 Giant congenital nevi exome sequencing Other
2020-07-09
EGAS00001004542 Gene expression profiling of nasopharyngeal carcinoma Other
2020-07-09
EGAS00001004544 MGMT genomic rearrangements contribute to chemotherapy resistance in gliomas Other
2020-07-12
EGAS00001004545 Conserved interferon-gamma signaling and decreased immune exclusion programs in responses to immune checkpoint blockade therapy Other
2020-07-12
EGAS00001004546 Survival Benefit and Genetic Profile of Pemetrexed as Initial Chemotherapy in Selected Chinese Patients with Advanced Lung Adenocarcinoma Other
2020-07-13
EGAS00001004548 A Multifactorial Tumor and Immune Cell Profile Determines Response to Immune Checkpoint blockade in Melanoma Other
2020-07-13
EGAS00001004550 Therapeutic vulnerabilities in the DNA damage response for the treatment of ATRX mutant neuroblastoma Other
2020-07-14
EGAS00001004551 Super enhancers define regulatory subtypes and cell identity in neuroblastoma Other
2020-07-14
EGAS00001004552 Super enhancers define regulatory subtypes and cell identity in neuroblastoma - RNA-seq Other
2020-07-14
EGAS00001004554 Prospective high-throughput genome profiling in advanced cancers: Other
2020-07-15
EGAS00001004555 Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma - CM67 WES Other
2020-07-16
EGAS00001004556 Novel mutations in TOP2A in gliomas Other
2020-07-20
EGAS00001004557 The Genomic Landscape of Prostate Cancer Brain Metastases Cancer Genomics
2020-07-20
EGAS00001004558 Deep MRD profiling defines outcome and unveils different modes of treatment resistance in standard and high risk myeloma Cancer Genomics
2020-07-21
EGAS00001004559 Profiling Genome-Wide DNA Methylation Patterns in Human Aortic and Mitral Valves Epigenetics
2020-07-21
EGAS00001004561 Cell types of the human retina and its organoids at single-cell resolution. Cowan et al Other
2020-07-21
EGAS00001004562 RNASeq of PDX and CDX tumours treated with ADC Other
2020-07-21
EGAS00001004564 Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma Other
2020-07-22
EGAS00001004567 Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma - CM066-WES Other
2020-07-23
EGAS00001004570 BELOB: Ribo-minus RNA-seq data corresponding to 96x GBM samples from the BELOB trial. Other
2020-07-23
EGAS00001004571 ScRNA-seq of PBMC and whole blood samples reveals a dysregulated myeloid cell compartment in severe COVID-19 Other
2020-07-24
EGAS00001004572 Whole genome, transcriptome and methylome profiling enhances actionable target discovery in high-risk paediatric cancer Other
2020-07-24
EGAS00001004574 Measurable residual disease in elderly acute myeloid leukemia: results from the PETHEMA-FLUGAZA phase III clinical trial Other
2020-07-24
EGAS00001004575 Exome and transcriptome sequencing of Desmoplastic Small Round Cell Sarcoma Other
2020-07-26
EGAS00001004576 Single cell RNA sequencing of CD19 CAR T-cell infusion products Other
2020-07-26
EGAS00001004578 Exome sequencing of paired primary tumor and metastatic breast cancer Other
2020-07-28
EGAS00001004582 TransNEO neoadjuvant breast cancer study Cancer Genomics
2020-07-29
EGAS00001004583 Hydroxycarbamide effect on DNA methylation and gene expression in MPN patients Other
2020-07-29
EGAS00001004584 Functional screening on patient-derived organoids identifies a therapeutic bispecific antibody that triggers EGFR degradation in LGR5+ tumor cells Other
2020-07-29
EGAS00001004585 RNA sequencing of chondrosarcoma Other
2020-07-29
EGAS00001004586 Cerebral organoid model reveals excessive proliferation of human caudal late interneuron progenitors in Tuberous Sclerosis Complex Other
2020-07-30
EGAS00001004587 Project MinE Illumina Infinium HumanMethylation450 (450k) BeadChip data on 2,790 Dutch whole blood samples, including 1,761 ALS patients of which 119 are known carriers of the C9orf72 repeat expansion. Other
2020-07-30
EGAS00001004588 Mutational signatures in head and neck cancer (H019) Other
2020-07-31
EGAS00001004592 SNP array files, IDAT files, from 34 members of a Family with a high prevalence of psychosis Other
2020-08-01
EGAS00001004593 Somatic mutations in healthy and leukemic blood progenitors reveal evolutionary mechanisms underlying childhood leukemia and differential patient outcome Cancer Genomics
2020-08-03
EGAS00001004594 Molecular sub-classification of hormone receptor-positive breast cancer Other
2020-08-05
EGAS00001004595 Using human induced pluripotent stem cell-derived oligodendrocytes to explore cellular phenotypes associated with t(1;11) translocation. Other
2020-08-05
EGAS00001004596 A GWAS for cutaneous leishmaniasis in Brazil Other
2020-08-06
EGAS00001004597 Gene expression profiles of disseminated breast cancer cells Transcriptome Analysis
2020-08-06
EGAS00001004599 Whole Exome Sequences from Iberian Roma samples Other
2020-08-06
EGAS00001004600 A Universal Gut Metagenomic-Derived Signature Predicts Cirrhosis Other
2020-08-06
EGAS00001004601 The endometrial transcription landscape of MRKH syndrome Other
2020-08-07
EGAS00001004603 Whole Exome Sequencing of High grade T1 non-muscle invasive bladder cancer Other
2020-08-09
EGAS00001004610 RRBS MDACC Lung PreCancer Other
2020-08-14
EGAS00001004611 Prime editing for functional repair in patient-derived disease models Other
2020-08-14
EGAS00001004612 High throughput profiling of undifferentiated pleomorphic sarcomas identifies two main subgroups with distinct immune contexture, clinical outcome and sensitivity to targeted therapies Cancer Genomics
2020-08-14
EGAS00001004613 PCa-LINES Other
2020-08-17
EGAS00001004614 Patient-tailored design for selective co-inhibition of leukemic cell subpopulations Other
2020-08-17
EGAS00001004615 Plasma ctDNA is a tumor tissue surrogate and enables clinical-genomic stratification of metastatic bladder cancer Cancer Genomics
2020-08-17
EGAS00001004619 Queensland Melanoma Genomic Biomarker Study Other
2020-08-19
EGAS00001004620 Understanding_hematopoietic_stem_cell_mobilization_and_engraftment_ Whole Genome Sequencing
2020-08-20
EGAS00001004621 SureTypeSC - accurate genotyping of single-cell SNP array data Other
2020-08-20
EGAS00001004623 Single-cell RNA-seq of celiac disease-specific plasma cells Other
2020-08-20
EGAS00001004624 16 Year Life History and Genomic Evolution of an ER+ HER2- Breast Cancer Other
2020-08-20
EGAS00001004625 The Genetic Basis of Preeclampsia in an Andean Population Adapted to High Altitude Population Genomics
2020-08-21
EGAS00001004627 GWAS in bullous pemphigoid in Germans Other
2020-08-21
EGAS00001004629 Hepatitis B virus integrations promote local and distant oncogenic driver alterations in hepatocarcinogenesis Other
2020-08-24
EGAS00001004630 Targeted sequencing of breast cancer susceptibility genes for 1,995 Japanese breast cancer patients Other
2020-08-24
EGAS00001004632 Mutational landscape of eccrine porocarcinoma (sweat gland tumour) Other
2020-08-24
EGAS00001004633 RNA-seq data of HGG PDOX study RNASeq
2020-08-24
EGAS00001004636 Detection of ctDNA in Plasma of Patients with Clinically Localised Prostate Cancer is Associated with Rapid Disease Progression Other
2020-08-25
EGAS00001004638 Molecular classification improves risk assessment in adult B-lineage ALL: Patients on the international UKALLXII-ECOG2993 trial. Other
2020-08-25
EGAS00001004639 Population Genomics of Native Americans from Andes and Amazon Population Genomics
2020-08-25
EGAS00001004640 The proliferative history shapes the DNA methylome of B-cell tumor and predicts clinical outcome Other
2020-08-26
EGAS00001004641 Characterization of stromal tumor-infiltrating lymphocytes and genomic alterations in metastatic lobular breast cancer Cancer Genomics
2020-08-26
EGAS00001004642 Genomewide detection of cytosine methylation by single molecule real-time sequencing Other
2020-08-27
EGAS00001004646 RNA sequencing of follicular T cell lymphoma Cancer Genomics
2020-08-31
EGAS00001004647 Analysis of transcriptomic profiles from affected and recovered muscle biopsies from children with reversible infantile respiratory chain deficiency. Other
2020-08-31
EGAS00001004648 Molecular Tumor Board to Inform on Personalized Medicine for a Man with Advanced Prostate Cancer Other
2020-08-31
EGAS00001004649 Targeted sequencing of Burkitt lymphoma tumour samples from the UK's Haematological Malignancy Research Network Other
2020-09-01
EGAS00001004650 Genome-wide information of Peruvian Native American Population Genomics
2020-09-02
EGAS00001004651 Cerebrospinal fluid circulating tumour DNA allows the characterisation and monitoring of medulloblastoma Other
2020-09-02
EGAS00001004653 Single nucleus and in situ RNA sequencing reveals cell topographies in the human pancreas Other
2020-09-02
EGAS00001004654 Exome sequencing of DNA from pituitary neuroendocrine tumor (PitNET) and germline DNA from the same patient Other
2020-09-03
EGAS00001004655 An Integrated Approach to Patient Stratification and Therapy Selection in Acute Myeloid Leukemia Cancer Genomics
2020-09-04
EGAS00001004656 Single cell RNA-sequencing of GSCs and GBM tumours Other
2020-09-05
EGAS00001004657 Tissue-specific cell-free DNA degradation quantifies circulating tumor DNA burden Other
2020-09-08
EGAS00001004659 Molecular and functional profiling of plasmablastic lymphoma Other
2020-09-09
EGAS00001004660 Aggressive PDACs show hypomethylation of repetitive elements and the execution of an intrinsic IFN program linked to a ductal cell-of-origin Cancer Genomics
2020-09-09
EGAS00001004661 scRNA-seq of patient-derived PDAC organoids Other
2020-09-09
EGAS00001004662 Chromothripsis in human breast cancer (HIPO K26K/H017/A017) Other
2020-09-11
EGAS00001004663 Targeting AXL Kinase Uniquely Sensitizes Therapy-Insensitive Leukemic Stem and Progenitor Cells to Venetoclax Treatment in Acute Myeloid Leukemia Other
2020-09-13
EGAS00001004664 Tumour gene expression signature in primary melanoma predicts long-term outcomes: A prospective multicentre study Other
2020-09-14
EGAS00001004665 Human breast transcriptome analysis Other
2020-09-14
EGAS00001004666 Genomic analysis of patient-derived xenograft models reveals intratumor-heterogeneity in endometrial cancer and can predict tumor growth inhibition with talazoparib Other
2020-09-15
EGAS00001004668 Transcriptomic intra-tumor heterogeneity of colorectal cancer varies depending on tumor location within the colorectum Other
2020-09-15
EGAS00001004669 Exploration of coding and non-coding variants in cancer using GenomePaint. Other
2020-09-15
EGAS00001004670 Copy number profiling of circulating cell-free DNA from high grade serous ovarian cancer patients Cancer Genomics
2020-09-17
EGAS00001004671 TCR β-chain repertoire characterization of regulatory and conventional T cells in breast tumors from breast cancer patients. Other
2020-09-17
EGAS00001004672 mutational landscape of normal human breast Other
2020-09-17
EGAS00001004673 Genomic profiling of patient-derived xenografts and organoids in prostate cancer Cancer Genomics
2020-09-17
EGAS00001004674 Foetal_phylogeny_8pcw___WGS_of_LCM_tissues Other
2020-09-17
EGAS00001004675 Transcriptomic profiling of patient-derived xenografts and organoids in prostate cancer Transcriptome Analysis
2020-09-18
EGAS00001004677 Organoid_Derivation_Project___GRCh38___RNAseq Other
2020-09-18
EGAS00001004680 Multifocal ileal NETs study WES Exome Sequencing
2020-09-21
EGAS00001004681 Multifocal ileal NETs study WGS HFF7VCCXY Whole Genome Sequencing
2020-09-21
EGAS00001004682 International consensus definition of DNA methylation subgroups in juvenile myelomonocytic leukemia Other
2020-09-21
EGAS00001004683 Molecular analysis of FIT interval colorectal cancers Other
2020-09-21
EGAS00001004684 Allele-specific expression of GATA2 due to epigenetic dysregulation in double mutated CEBPA AML Other
2020-09-21
EGAS00001004686 Molecular analysis of post-colonoscopy CRC (PCCRC) Other
2020-09-22
EGAS00001004689 COVID-19 Postmortem Lung snRNA-seq Other
2020-09-22
EGAS00001004693 UROMOL 2020 - RNA-seq data Other
2020-09-24
EGAS00001004694 Regulatory T cell transcriptomic reprogramming characterizes adverse events by checkpoint inhibitors in solid tumors Other
2020-09-24
EGAS00001004695 Human gastrointestinal epithelia of the esophagus, stomach and duodenum resolved at single-cell resolution Other
2020-09-25
EGAS00001004696 Nuclease deficiencies alter plasma cell-free DNA methylationprofiles (mouse) Other
2020-09-27
EGAS00001004697 Ultraviolet radiation drives mutations in a subset of mucosal melanomas Other
2020-09-29
EGAS00001004700 Network-based systems pharmacology identifies heterogeneity in LCK and BCL2 signaling and differential vulnerability of T-cell acute lymphoblastic leukemia to targeted therapy Other
2020-10-02
EGAS00001004701 Integrative Analysis of Pediatric Acute Leukemia Identifies Acute Myeloid/T-Lymphoblastic Leukemia Subtype that Spans a T Lineage and Myeloid Continuum with Distinct Prognoses Other
2020-10-02
EGAS00001004702 Chromosomal copy number heterogeneity predicts survival rates across cancers Other
2020-10-05
EGAS00001004704 A comprehensive characterization of the cell-free transcriptome reveals tissue- and subtype-specific biomarkers for cancer detection Other
2020-10-06
EGAS00001004705 Whole genome sequencing of EBV Associated Nasopharyngeal Carcinoma Other
2020-10-07
EGAS00001004706 Pancreatic cancer RNA sequencing Cancer Genomics
2020-10-07
EGAS00001004707 Resident memory CD8 T cell in human lung cancer RNASeq
2020-10-07
EGAS00001004709 A novel orthotopic patient-derived xenograft model of radiation-induced glioma following medulloblastoma Other
2020-10-09
EGAS00001004710 Genome-wide somatic variants in CRC (GRCh38) Whole Genome Sequencing
2020-10-09
EGAS00001004712 Organoid_Derivation_Project___GRCh38___WGS Other
2020-10-11
EGAS00001004714 Transcriptome Sequencing Data of High Grade Serous Ovarian Cancer Other
2020-10-12
EGAS00001004717 Single-cell RNA sequencing of bronchoalveolar lavages from COVID-19 patients Other
2020-10-13
EGAS00001004718 CAR_T_cell_Study Transcriptome Analysis
2020-10-13
EGAS00001004719 STAT5 is a therapeutically targetable vulnerability in cutaneous T-cell lymphoma Other
2020-10-13
EGAS00001004722 HCA_Placental_Infection_Atlas Other
2020-10-14
EGAS00001004723 HCA_Gonads_Foetal_EU_H2020_HUGODECA_RNA Other
2020-10-14
EGAS00001004724 Multiomics Characterization of Low-grade Serous Ovarian Carcinoma Other
2020-10-14
EGAS00001004727 HCA_Female_Reproductive_Adult_WSSS_RNA Transcriptome Analysis
2020-10-14
EGAS00001004728 Microbiota 16S sequencing study in NSCLC patients eligible for surgery without neoadjuvant treatment Other
2020-10-15
EGAS00001004729 Multi Omics of glioma in the the Chinese Glioma Genome Atlas (CGGA) project Cancer Genomics
2020-10-15
EGAS00001004733 Mutational Landscape and Tumor Burden Assessed by Cell-Free DNA in Diffuse Large B-Cell Lymphoma: a Population-based Study Other
2020-10-16
EGAS00001004734 Identification of rare germline variants in familial multiple myeloma Other
2020-10-16
EGAS00001004735 Multi-region whole-exome sequencing of 10 neuroblastoma cases Other
2020-10-16
EGAS00001004736 Study of tumor RNA expression differences between treated and untreated PitNET patients Other
2020-10-16
EGAS00001004739 Prognostic and therapeutic significance of leukemia subtypes and minimal residual disease measurements in pediatric acute lymphoblastic leukemia treated with contemporary risk-directed trial: a cohort study Other
2020-10-16
EGAS00001004740 Single Cell ATAC-Seq on human cord-blood derived HSPC. Epigenetics
2020-10-16
EGAS00001004741 ATAC-Seq and CTCF ChIP-Seq on the OCIAML-2 cell line Epigenetics
2020-10-16
EGAS00001004742 Bulk ATAC-Seq on sorted cord blood hematopoietic populations Epigenetics
2020-10-16
EGAS00001004743 Hi-C on the OCIAML-2 Cell Line Epigenetics
2020-10-16
EGAS00001004744 Low-C on Human CB-derived LT-HSC and ST-HSC Epigenetics
2020-10-16
EGAS00001004745 RNA_Seq on Human CB-derived LT-HSC with shCTCF or control vector RNASeq
2020-10-16
EGAS00001004746 Extramammary Paget Disease Other
2020-10-19
EGAS00001004748 Small molecule screen reveals synergy of cell cycle checkpoint kinase inhibitors with DNA-damaging chemotherapies in medulloblastoma (RNAseq dataset) RNASeq
2020-10-19
EGAS00001004749 DIPG RNA and exome sequencing Other
2020-10-19
EGAS00001004750 The evolution of adult T-cell acute lymphoblastic leukemia Other
2020-10-19
EGAS00001004751 Characterization of T cell tumor infiltration in brain metastases through the analysis of the cerebrospinal fluid Cancer Genomics
2020-10-19
EGAS00001004752 Genetic ancestry contributes to somatic mutations in lung cancers from admixed Latin American populations Other
2020-10-19
EGAS00001004753 Mutation-specific non-canonical pathway of PTEN as a distinct therapeutic target for glioblastoma Other
2020-10-20
EGAS00001004754 Investigate the evolutionary trajectories during invasiveness acquisition in early lung adenocarcinoma Other
2020-10-20
EGAS00001004755 Rucaparib in patients presenting a metastatic breast cancer with Homologous Recombination Deficiency, without germline BRCA1/2 mutation, pronostic value of high LOH genomic score and predictive value of HRDetect (microarray) Other
2020-10-20
EGAS00001004756 Rucaparib in patients presenting a metastatic breast cancer with Homologous Recombination Deficiency, without germline BRCA1/2 mutation, pronostic value of high LOH genomic score and predictive value of HRDetect (WGS) Whole Genome Sequencing
2020-10-20
EGAS00001004757 Much ado about nothing? - Off-target amplification can lead to false positive bacterial brain microbiome detection in healthy and Parkinson's disease individuals Other
2020-10-20
EGAS00001004758 The transition from normal lung anatomy to minimal and established fibrosis in Idiopathic Pulmonary Fibrosis RNASeq
2020-10-21
EGAS00001004760 Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing Other
2020-10-22
EGAS00001004763 Dynamics of genome architecture and chromatin function during human B cell differentiation and neoplastic transformation Other
2020-10-22
EGAS00001004764 Immunological hallmarks for clinical response to BCG in bladder cancer Other
2020-10-23
EGAS00001004765 Metabolic requirements of the metastasis-initiating tumour cell population using oral squamous cell carcinoma (OSCC) as a model system Cancer Genomics
2020-10-26
EGAS00001004766 Epigenome-wide association study of asthma remission in whole blood and nasal epithelium Epigenetics
2020-10-26
EGAS00001004767 Overactivation of the IGF signalling pathway in osteosarcoma Other
2020-10-26
EGAS00001004768 RNA-seq of uncultured CD112high and CD112low long-term(LT) human hematopoietic stem cells (HSC) and cultured and lentiviral transduced (CTRL, INKA1-OE) LT- and short-term HSC from umbilical cord blood Other
2020-10-26
EGAS00001004769 Single cell RNA-sequencing (scRNA-seq) of the human hematopoietic stem cell compartment (CD34+CD38-CD45RA-) Other
2020-10-26
EGAS00001004770 Transcriptomic profiling of prostate cancer metastasis xenograft models reveals conservation of bone microenvironment signatures Transcriptome Analysis
2020-10-29
EGAS00001004771 Paediatric_CNS_tumour_autopsy_DNA Other
2020-10-29
EGAS00001004772 Hypertension delays viral clearance and exacerbates airway hyperinflammation in patients with COVID-19 Other
2020-10-29
EGAS00001004773 Colorectal cancer cells possess an equipotent capacity to enter a developmental pausing-like state to survive chemotherapy Cancer Genomics
2020-10-29
EGAS00001004777 Second hit rare genetic variants in families with seemingly GBA gene associated Parkinson’s disease Whole Genome Sequencing
2020-11-02
EGAS00001004780 Cell of Origin and Early Evolution of Leukemia in Down Syndrome Other
2020-11-02
EGAS00001004781 Neuroblastoma tumor heterogeneity and cell plasticity (from PDX and cell lines) Other
2020-11-03
EGAS00001004782 Gene expression from human iPSC derived cortical neurons Other
2020-11-03
EGAS00001004783 Rna-Seq Leiomyosarcoma subtypes Other
2020-11-04
EGAS00001004784 Mechanisms of active DNA demethylation in human monocytes Epigenetics
2020-11-04
EGAS00001004786 Genomics-based personalized oncology in cancer of unknown primary (CUP, project H021) Other
2020-11-06
EGAS00001004788 Methylation analysis for plasma DNA of patients with organ transplantation Other
2020-11-09
EGAS00001004789 MutationalPatterns2: The one stop shop for the analysis of mutational processes: DNA repair deletions Whole Genome Sequencing
2020-11-09
EGAS00001004791 Familial psychosis associated with a missense mutation at MACF1 gene combined with the rare duplications DUP3p26.3 and DUP16p23.3, affecting the CNTN6 and CDH13 genes Other
2020-11-11
EGAS00001004792 RNA-seq study of a Princess Margaret Cancer Centre human acute myeloid leukemia patient cohort Other
2020-11-11
EGAS00001004793 Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia Other
2020-11-12
EGAS00001004794 RNAseq cutaneous and uveal melanoma liver metastases Other
2020-11-12
EGAS00001004795 WES cutaneous and uveal melanoma liver metastases Other
2020-11-12
EGAS00001004796 Neuroblastoma Cell Line Circle-seq Other
2020-11-12
EGAS00001004797 Primary Neuroblastoma Circle-seq Other
2020-11-12
EGAS00001004798 RNA-seq study of human long-term and short-term hematopoietic stem cells from umblical cord blood with lentiviral overexpression of S1PR3 Other
2020-11-12
EGAS00001004800 BRCA2, ATM, and CDK12 defects differentially shape prostate tumor driver genomics and clinical aggression Cancer Genomics
2020-11-13
EGAS00001004805 Single cell RNA sequencing of relapsed/refractory multiple myeloma Other
2020-11-13
EGAS00001004808 CTCF-dependent enhancer hijacking by the EVI1 oncogene in leukemia Other
2020-11-13
EGAS00001004809 BIOKEY: A single-cell catalogue of the dynamic changes underlying Checkpoint Immunotherapy response in Early Breast Cancer Other
2020-11-15
EGAS00001004810 BCL11B enhancer hijacking defines a subtype of lineage ambiguous stem cell leukemia Other
2020-11-15
EGAS00001004812 Integrative multi-omic analyses of malignant pleural mesothelioma Other
2020-11-16
EGAS00001004813 Comprehensive Genomic and Transcriptomic Analysis of Rare Cancers for Guiding of Therapy (H021) Other
2020-11-16
EGAS00001004814 Transcriptional profiling of ovarian tumours and cell lines Other
2020-11-16
EGAS00001004816 DNA polymerase and mismatch repair deficient cancers exert distinct genome-wide microsatellite signatures 2 Whole Genome Sequencing
2020-11-16
EGAS00001004819 Long-read and short-read isoform sequencing in breast cancer Other
2020-11-17
EGAS00001004820 Gut metagenomic data of 2,338 Pinggu adults Other
2020-11-18
EGAS00001004821 Integrated Genomic and Transcriptomic Analysis Reveals Unique Characteristics of Hepatic Metastases and Pro-metastatic Role of Complement C1q in Pancreatic Ductal Adenocarcinoma Cancer Genomics
2020-11-18
EGAS00001004824 Reconstruction of human phylogenetic trees using single-cell genome sequencing Other
2020-11-19
EGAS00001004825 Molecular response of AML blasts to Aza-treatment. Other
2020-11-20
EGAS00001004826 The genetic structure of Norway Other
2020-11-20
EGAS00001004827 Volasertib preclinical activity in high-risk hepatoblastoma Other
2020-11-20
EGAS00001004828 Alveolar Rhabdomyosarcoma case report Other
2020-11-20
EGAS00001004829 scRNA-seq of HGSC tumor and ascites Other
2020-11-23
EGAS00001004830 MicroRNAs signatures from CSF extracellular vesicles of Parkinson’s Disease patients RNASeq
2020-11-23
EGAS00001004832 OpACIN-neo – A Multicenter Phase 2 Study to identify the Optimal neo-Adjuvant Combination scheme of Ipilimumab and Nivolumab – Whole exome sequencing Other
2020-11-24
EGAS00001004833 OpACIN-neo – A Multicenter Phase 2 Study to identify the Optimal neo-Adjuvant Combination scheme of Ipilimumab and Nivolumab – RNA sequencing Other
2020-11-24
EGAS00001004835 Differential gene expression in the colon mucosa of irritable bowel syndrome patients with mixed type symptoms Other
2020-11-24
EGAS00001004836 Effect_of_FAM50_knockout_on_the_transcriptome Cancer Genomics
2020-11-24
EGAS00001004837 Inherited CD28 deficiency in otherwise healthy patients with disseminated warts and giant horns Transcriptome Analysis
2020-11-24
EGAS00001004838 WGSPD Project 3 - Genomic Strategies to Identify High-impact Psychiatric Risk Variants Whole Genome Sequencing
2020-11-24
EGAS00001004839 An essential role for MYB in driving oncogenic EVI1 expression in enhancer-rearranged leukemias Other
2020-11-25
EGAS00001004841 Molecular profiling of an AML case following treatment with a BCL2 inhibitor Other
2020-11-26
EGAS00001004843 Immune trajectory of response and adverse effect in immunotherapy-treated hepatocellular carcinoma Other
2020-11-27
EGAS00001004844 Single Cell MK and HSC sequencing Other
2020-11-27
EGAS00001004847 Circulating Tumor DNA in Checkpoint Inhibitor treated Lung Cancer Other
2020-11-30
EGAS00001004850 The Acquisition of Molecular Drivers in Pediatric Therapy-Related Myeloid Neoplasms Other
2020-11-30
EGAS00001004851 AGECAN - Interespecies conservation of brain specific DNA methylation in aging and cancer Epigenetics
2020-11-30
EGAS00001004852 Tumor HTG EdgeSeq from metastatic castrate resistant prostate cancer Other
2020-12-01
EGAS00001004856 Shwachman-Diamond syndrome sequencing study Other
2020-12-01
EGAS00001004857 Comprehensive genomic and transcriptomic analysis of three synchronous primary tumours and a recurrence from a head and neck cancer patient Other
2020-12-01
EGAS00001004860 PBMC gene expression profiles in diet treated celiac disease upon oral gluten challenge Transcriptome Analysis
2020-12-01
EGAS00001004861 Bulk-RNA Sequencing of high-grade pancreatic and non-pancreatic Neuroendocrine Neoplasms Other
2020-12-02
EGAS00001004862 UROMOL 2020 - SNP data Other
2020-12-02
EGAS00001004863 Microsatellite instability at U2AF-binding polypyrimidic tract sites perturbs alternative splicing during colorectal cancer initiation Cancer Genomics
2020-12-02
EGAS00001004864 Genomic analysis of a hypermutated gliosarcoma Other
2020-12-02
EGAS00001004867 Targeted de-methylation of the FOXP3-TSDR Other
2020-12-03
EGAS00001004868 Genetic makeup of agnospheres Other
2020-12-03
EGAS00001004869 POPCOL: population-based colonoscopy. Other
2020-12-03
EGAS00001004870 NIHR BioResource Common Disease Patients 2016 Other
2020-12-03
EGAS00001004871 Single-cell multi-omic profiling of glioblastoma-associated myeloid cells Transcriptome Analysis
2020-12-03
EGAS00001004872 Biological and Therapeutic Implications of a Unique Subtype of NPM1 Mutated AML Cancer Genomics
2020-12-03
EGAS00001004877 Accurate detection of tumor-specific fusion genes reveals strongly immunogenic personal neo-antigens Other
2020-12-07
EGAS00001004878 Pancreatic, Small-intestinal and Pulmonary Neuroendocrine Tumors Other
2020-12-08
EGAS00001004879 Targeted Sequencing of Shwachman-Diamond syndrome bone marrow samples Other
2020-12-08
EGAS00001004880 Whole Exome sequencing data from Shwachman-Diamond syndrome bone marrow samples Exome Sequencing
2020-12-08
EGAS00001004881 Single cell sequencing data from Shwachman-Diamond syndrome bone marrow Other
2020-12-08
EGAS00001004882 Somatic_evolution_in_the_psoriatic_skin Other
2020-12-09
EGAS00001004884 Molecular evolution and clinical trajectories of prostate cancer identifies novel markers for risk stratification - additional data Cancer Genomics
2020-12-09
EGAS00001004885 Gut microbiome sequencing in patients receiving combination immune checkpoint blockade Other
2020-12-10
EGAS00001004886 mRNA and T cell receptor sequencing of patients with Pandemrix-associated narcolepsy type 1 Other
2020-12-10
EGAS00001004887 EAC Genomic data Cancer Genomics
2020-12-10
EGAS00001004888 Patterns of transcription factor programs and immune pathway activation define four major subtypes of SCLC with distinct therapeutic vulnerabilities Other
2020-12-10
EGAS00001004889 Multi-omics profiling of PSCCE Other
2020-12-11
EGAS00001004890 Impact of BRCA mutation type in non-tumorous breast tissue transcriptome Other
2020-12-11
EGAS00001004892 Targeted sequencing DDR genes in cancer stem cells Other
2020-12-11
EGAS00001004894 Single cell T cell Landscape and T Cell Receptor Repertoire Profiling of AML in Context of PD-1 Blockade Therapy Other
2020-12-11
EGAS00001004895 Risk and modifying factors in Frontotemporal Dementia Other
2020-12-12
EGAS00001004897 Nuclease deficiencies alter plasma cell-free DNA methylationprofiles (Human) Other
2020-12-13
EGAS00001004899 Personalised therapy with MEK inhibition leads to a sustained complete response in an adolescent patient with a recurrent malignant peripheral nerve sheath tumor Other
2020-12-14
EGAS00001004900 Single-cell chromatin accessibility landscape identifies tissue repair program in human regulatory T cells Other
2020-12-14
EGAS00001004902 Whole genome sequencing of germline DNA from 8 patients with adult granulosa cell tumors (from blood or saliva) Other
2020-12-14
EGAS00001004903 Finding structural variation and functional consequences from the primary leukemia cells (AML) at the single-cell level Other
2020-12-14
EGAS00001004904 Oncolytic virotherapy mediated anti-tumor response in primary cutaneous B-cell lymphoma: a single-cell perspective RNASeq
2020-12-14
EGAS00001004905 Dual targeting of polyamine synthesis and uptake in diffuse intrinsic pontine gliomas Other
2020-12-15
EGAS00001004906 Mutational Landscape of Plasmablastic Lymphoma Other
2020-12-15
EGAS00001004907 Blood RNA-seq from Mexican DMD patients and healthy controls Other
2020-12-15
EGAS00001004908 Mutations in SKI in Shprintzen-Goldberg syndrome lead to attenuated TGFB responses through SKI stabilization RNASeq
2020-12-15
EGAS00001004909 Single cell multi-omic data of glioblastoma evolution under therapy Other
2020-12-16
EGAS00001004912 Neutrophils infected with Leishmania donovani Other
2020-12-17
EGAS00001004913 ChIP-seq of plasma cell-free nucleosomes identifies gene expression programs of the cells-of-origin Other
2020-12-17
EGAS00001004915 Selective Elimination of Immunosuppressive T cells in Patients with Multiple Myeloma Cancer Genomics
2020-12-17
EGAS00001004918 Oxford Nanopore RNA sequencing for HLA typing Other
2020-12-18
EGAS00001004925 Finding structural variation and functional consequences from the primary leukemia cells (CLL) at the single-cell level Other
2020-12-20
EGAS00001004926 Mutational consequences of hematopoietic stem cell transplantation in humans Whole Genome Sequencing
2020-12-21
EGAS00001004927 Short and long-read sequencing of Brugada syndrome samples Other
2020-12-21
EGAS00001004928 Single-cell RNA-seq of bronchoalveolar lavage (BAL) fluid in severe COVID-19 and SARS-CoV-2 stimulated classical blood monocytes Other
2020-12-23
EGAS00001004929 Whole genome sequencing delineates regulatory, structural, and cryptic splice variants in early onset cardiomyopathy Other
2020-12-23
EGAS00001004930 Phase Ib of olaparib and capivasertib Other
2020-12-25
EGAS00001004931 Illumina RNA sequencing for HLA expression qauntification Other
2020-12-28
EGAS00001004933 The Genetic History of Greenlandic-European contact Other
2020-12-31
EGAS00001004934 Detection of Gene Fusions using Targeted Next-Generation Sequencing – a Comparative Evaluation Cancer Genomics
2021-01-04
EGAS00001004935 Single Cell Dissection of the Tumour Microenvironment Reveals Dynamic Interplay Shaping the Tumour Immunity Continuum in Ovarian Cancer Other
2021-01-05
EGAS00001004936 Single-cell analysis of the multicellular ecosystem in viral carcinogenesis by HTLV-1 Other
2021-01-05
EGAS00001004939 Tissue and plasma RNA from esophageal cancer and precursor lesions Other
2021-01-06
EGAS00001004940 Sensitive and robust liquid biopsy-based detection of PIK3CA mutations Other
2021-01-06
EGAS00001004941 Genomic insights into the pathogenesis of Epstein-Barr virus-associated diffuse large B-cell lymphoma by whole-genome and targeted amplicon-based sequencing Other
2021-01-06
EGAS00001004942 Multi-institutional collaboration to characterize 5hmC in prostate cancer, both tumor biopsies and cfDNA. Other
2021-01-06
EGAS00001004943 Single-cell RNA sequencing reveals the mesangial identity and species diversity of glomerular cell transcriptomes Other
2021-01-06
EGAS00001004944 Fasting-mimicking diet reshapes antitumor immunity in cancer patients RNASeq
2021-01-07
EGAS00001004946 Endothelium-derived stromal cells contribute to bone marrow niche formation Other
2021-01-09
EGAS00001004947 Genetic insights into the biological mechanisms governing human ovarian ageing Other
2021-01-11
EGAS00001004948 BCR Signaling in human BM PC Other
2021-01-11
EGAS00001004949 Comparison of the diagnostic yield of aCGH and NGS across different neurodevelopmental disorders Other
2021-01-11
EGAS00001004950 CASCADE metastatic melanoma study Other
2021-01-12
EGAS00001004951 Upper respiratory microbiome of COVID-19 patients Other
2021-01-12
EGAS00001004953 The temporal mutational and immune tumour microenvironment remodelling of HER2-negative primary breast cancers Other
2021-01-13
EGAS00001004956 Converging and evolving immuno-genomic routes towards immune escape in breast cancer Cancer Genomics
2021-01-14
EGAS00001004959 GCP study Cancer Genomics
2021-01-14
EGAS00001004960 Sequencing of cell-free DNA from breast cancer patients Other
2021-01-15
EGAS00001004961 Copy number and mutation profiling of Stage 1 epithelial ovarian cancer biopsies Other
2021-01-15
EGAS00001004962 Cell-free DNA TAPS for early cancer detection Other
2021-01-15
EGAS00001004963 Assessment of cannabidiol and Δ9-tetrahydrocannabiol in mouse models of medulloblastoma Other
2021-01-16
EGAS00001004964 Preliminary Results from the Initiative for Molecular Profiling and Advanced Cancer Therapy 2 (IMPACT 2) Study Cancer Genomics
2021-01-18
EGAS00001004965 Evaluation of capture and amplicon-based targeted sequencing methods on formalin-fixed tumours Other
2021-01-18
EGAS00001004966 Multiomics analyses of Parkinson's disease midbrains Other
2021-01-18
EGAS00001004967 Transcriptomic analysis of TFEB knockdown in LT-HSC. Other
2021-01-18
EGAS00001004968 Transcriptomic analysis of human hematopoietic populations sorted from umbilical cord blood. Other
2021-01-18
EGAS00001004969 Transcriptomic analysis of TFEB overexpression in LT-HSC, ST-HSC and MEP Other
2021-01-18
EGAS00001004970 Transcriptomic analysis of MYC overexpression in LT-HSC. Other
2021-01-18
EGAS00001004971 Chromatin accessibility analysis of TFEB overexpression in LT-HSC Other
2021-01-18
EGAS00001004973 Application of short-RNA-seq in post-mortem human hippocampi from the Calgary Brain Bank (CBB) to assess transcriptome-wide deregulation in processing of SINE Alu RNAs in Alzheimer’s disease Other
2021-01-19
EGAS00001004974 Macrophage response in preterm infants compared to term infants Other
2021-01-19
EGAS00001004975 Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients Cancer Genomics
2021-01-19
EGAS00001004979 SNParray Other
2021-01-21
EGAS00001004982 Integrative Molecular Classification of Meningiomas Other
2021-01-21
EGAS00001004987 High-grade serous ovarian cancer refined with single-cell RNA-sequencing Other
2021-01-24
EGAS00001004988 RNA-sequencing of gluten-reactive and non-reactive T-cells from blood samples of treated CeD patients during a gluten-challenge Other
2021-01-24
EGAS00001004989 Single-cell T-cell receptor sequencing of intraepithelial CD8+ αβ T-cells in celiac disease Other
2021-01-24
EGAS00001004990 Evolutionary dynamics of neuroblastoma Other
2021-01-25
EGAS00001004992 Targeting the Epichaperome As an Effective Precision Medicine Approach in a Novel PML-SYK Fusion Acute Myeloid Leukemia Transcriptome Analysis
2021-01-26
EGAS00001004994 Somatic mutations in lymphocytes in patients with immune-mediated aplastic anemia Transcriptome Analysis
2021-01-27
EGAS00001004995 Peruvian Genome Project - Whole Genome Sequencing Other
2021-01-27
EGAS00001004996 Boson HCV infected liver bulk RNASeq study Other
2021-01-27
EGAS00001004997 Clinical outcomes in ctDNA-positive urothelial carcinoma patients treated with adjuvant immunotherapy Other
2021-01-27
EGAS00001004998 The genomic landscape of childhood acute lymphoblastic leukaemia with intrachromosomal amplification of chromosome 21 (iAMP21-ALL) Other
2021-01-28
EGAS00001004999 Whole genome sequencing of patients affected by acute intermittent porphyria Other
2021-01-28
EGAS00001005000 single cell sequencing of resting and Influenza-stimulated mononcluear phagocytes of African and Europeans with varying degree of ex-vivo susceptibility to Influenza Other
2021-01-28
EGAS00001005001 Relapse series of two Pediatric ALL patients Other
2021-01-29
EGAS00001005004 Fibromyalgia versus small fiber neuropathy: Diverse keratinocyte transcriptome signature Other
2021-01-29
EGAS00001005005 Genetic heterogeneity and dynamics of transcriptional subtypes in matched primary and recurrent head and neck squamous cell carcinomas Other
2021-01-30
EGAS00001005006 Longitudinal single-cell RNA-seq data of metastatic ovarian cancer Transcriptome Analysis
2021-01-30
EGAS00001005008 Mutations in the RAS/MAPK pathway drive replication repair deficient hypermutated tumors and confer sensitivity to MEK inhibition Other
2021-01-30
EGAS00001005009 DO NOT USE - Whole genome sequencing of SI-NETs from six patients Other
2021-01-31
EGAS00001005010 Longitudinal single-cell RNA-seq data of metastatic ovarian cancer Other
2021-01-31
EGAS00001005012 MBD4 targeted sequencing Other
2021-02-01
EGAS00001005013 Intratumoral plasma cells predict outcomes to PD-L1 blockade in non-small cell lung cancer Other
2021-02-01
EGAS00001005014 Primary prostate Hi-C Other
2021-02-01
EGAS00001005015 RNA sequencing of PTCL-NOS Cancer Genomics
2021-02-02
EGAS00001005018 Exome sequencing reveals pathogenic variants in known and novel candidate genes for severe sperm motility disorders Other
2021-02-02
EGAS00001005019 Longitudinal Single-Cell Profiling Reveals Molecular Heterogeneity and Tumor-Immune Evolution in Refractory Mantle Cell Lymphoma Other
2021-02-02
EGAS00001005020 Gut metagenome/FINRISK 2002 (Salosensaari et al. Nature Comms 2021) Other
2021-02-02
EGAS00001005021 Single cell RNAseq of lung adenocarcinoma Other
2021-02-03
EGAS00001005022 Deep genetic affinity between coastal Pacific and Amazonian natives evidenced by Australasian ancestry Other
2021-02-03
EGAS00001005023 Kalirin-RAC controls nucleokinetic migration in ADRN-type neuroblastoma Other
2021-02-03
EGAS00001005024 Proteotranscriptomic classification and characterization of pancreatic neuroendocrine neoplasms Other
2021-02-03
EGAS00001005025 Transcriptomic and epigentic analysis of human peripheral blood NK cell subsets revealing role of Bcl11b in differentiation Other
2021-02-04
EGAS00001005026 Summary statistics of meta-analysis using two genome-wide association study of inflammatory bowel disease in Koreans. Other
2021-02-04
EGAS00001005027 The Dutch Microbiome Project: Defining the (un)healthy gut microbiome Other
2021-02-05
EGAS00001005029 Monitoring of leukemia clones in B-cell acute lymphoblastic leukemia at diagnosis and during treatment by single-cell DNA amplicon sequencing Other
2021-02-08
EGAS00001005030 MicroRNA profiling by next-generation sequencing for colorectal cancer screening Other
2021-02-08
EGAS00001005032 Genomic Study of Gastric Cancer Other
2021-02-09
EGAS00001005033 The WID-EC test for the detection and risk prediction of endometrial cancer Epigenetics
2021-02-09
EGAS00001005034 Genome-wide characterization of Kuwaiti Arab Population Other
2021-02-09
EGAS00001005038 Gut metagenome/FR 2002 Other
2021-02-11
EGAS00001005039 SINGLE-CELL RNA SEQUENCING Single-cell RNA sequencing was performed on 13 ‘mild-moderate’ and 10 ‘critical’ COVID19 PBMC samples Other
2021-02-11
EGAS00001005040 A rare CTSC mutation in Papillon-Lefèvre Syndrome Other
2021-02-11
EGAS00001005041 Transcriptome analysis of PBMCs from patients with STAT1 activating mutation RNASeq
2021-02-11
EGAS00001005042 Test Study for EGA using data from 1000 Genomes Project - Phase 3 Whole Genome Sequencing
2021-02-11
EGAS00001005043 hereditary BrEAst Case CONtrol study Other
2021-02-11
EGAS00001005044 Single-cell roadmap of immune cell responses in chronic myeloid leukemia Other
2021-02-11
EGAS00001005045 The DNA methylome of cervical cells and risk of ovarian cancer Epigenetics
2021-02-12
EGAS00001005046 Using de novo assembly to identify structural variation of complex immune system gene regions Other
2021-02-12
EGAS00001005047 Single-cell TCR sequencing of gluten-specific T cells from 20 celiac disease patients uploaded on 2021 Other
2021-02-12
EGAS00001005048 Detection of low-frequency DNA variants by targeted sequencing of the Watson and Crick strands Other
2021-02-12
EGAS00001005049 Combining dasatinib and IFN-α in CML – immunomodulatory effects linked to treatment response and adverse events Other
2021-02-13
EGAS00001005050 UROMOL 2020 - RNA-seq data for validation Other
2021-02-15
EGAS00001005051 Bone marrow derived stromal cells from Myelodysplastic Syndromes Other
2021-02-15
EGAS00001005052 Whole-genome sequencing of a census-based elderly cohort of Brazilians Whole Genome Sequencing
2021-02-15
EGAS00001005053 Hermansky-Pudlak syndrome type 1 causes impaired anti-microbial immunity through a pathogenic lipid metabolism-mTOR circuit Other
2021-02-15
EGAS00001005054 Genetic analysis of HLA and immune escape genes in Diffuse Large B-cell Lymphoma Other
2021-02-15
EGAS00001005055 The WID-BC-index identifies women with primary poor prognostic breast cancer based on DNA methylation in cervical samples Other
2021-02-16
EGAS00001005057 Characterization of DLBCL with a PMBL gene expression signature Other
2021-02-17
EGAS00001005060 SARS-CoV-2 escapes CD8 T cell surveillance via mutations in MHC-I restricted epitopes [10x] Other
2021-02-18
EGAS00001005061 Stromal cell diversity associated with immune evasion in human triple‐negative breast cancer RNASeq
2021-02-18
EGAS00001005064 Mutational analysis of an oligoprogressive sarcomatoid hepatocellular carcinoma treated with an immune checkpoint inhibitor. Other
2021-02-19
EGAS00001005065 Genomic Landscape of Malignant Peripheral Nerve Sheath Tumor-like Melanoma Other
2021-02-19
EGAS00001005066 Single-cell RNA-seq data from metastatic ovarian cancer for quality control study Other
2021-02-22
EGAS00001005068 Discovery of cancer prognostic markers based on comparison of gene expression in colorectal cancer samples. Other
2021-02-22
EGAS00001005069 Sensitive and reproducible cell-free methylome quantification with synthetic spike-in controls Epigenetics
2021-02-22
EGAS00001005070 Breast tissue methylation analysis Epigenetics
2021-02-22
EGAS00001005071 Subtype-associated epigenomic landscape and 3D genome structure in bladder cancer Other
2021-02-23
EGAS00001005073 Whole-exome sequencing of hepatocellular carcinoma biopsies (proteogenomic study) Other
2021-02-23
EGAS00001005074 Transcriptome sequencing of hepatocellular carcinoma biopsies (proteogenomic study) Other
2021-02-23
EGAS00001005075 Clonal evolution and clinical implications of genetic abnormalities in blastic transformation of chronic myeloid leukaemia Other
2021-02-24
EGAS00001005076 Liverpool Preterm Birth Biomarker Study Other
2021-02-25
EGAS00001005077 Anal SCC cell line and parent tumour comparative whole exome sequencing Other
2021-02-26
EGAS00001005078 The WID-CIN test identifies women with, and at risk of, cervical intraepithelial neoplasia grade 3 and invasive cervical cancer (CIN3+) Other
2021-02-26
EGAS00001005081 Molecular analysis of inflammatory myofibroblastic tumor (WGS and WES) Cancer Genomics
2021-03-01
EGAS00001005083 Multiple migrations to the Philippines during the last 50,000 years Other
2021-03-01
EGAS00001005084 Clinical significance of novel subtypes of acute lymphoblastic leukemia in the context of minimal residual disease-directed therapy Other
2021-03-01
EGAS00001005085 Profiling of H3K27ac landscape in immune cells from rheumatoid arthritis patients and healthy controls Other
2021-03-02
EGAS00001005086 ARAF Mutations Confer Resistance to RAF Dimer Inhibitor Belvarafenib in NRAS- and BRAF- Mutant Melanoma Other
2021-03-02
EGAS00001005087 Whole exome sequencing from small cell lung cancer patients Exome Sequencing
2021-03-02
EGAS00001005090 A_cell_atlas_of_the_human_fetal_spine_SB_HDBR_Project_200532 Transcriptome Analysis
2021-03-04
EGAS00001005091 Enrichment of homologous recombination repair alteration in prostate cancer brain metastases Other
2021-03-04
EGAS00001005093 single-stranded DNA study Other
2021-03-04
EGAS00001005095 The_evolution_of_CML Other
2021-03-04
EGAS00001005096 Whole genome sequencing of 76 tumor and normal samples from 11 SI-NET patients Other
2021-03-04
EGAS00001005097 Oncogenic cooperation between the TCF7-SPI1 fusion and NRAS(G12D) requires β-catenin activity to drive T-cell acute lymphoblastic leukemia. Other
2021-03-05
EGAS00001005098 Hermansky-Pudlak syndrome type 1 causes impaired anti-microbial immunity through a pathogenic lipid metabolism-mTOR circuit - 10x Genomics scRNAseq Other
2021-03-05
EGAS00001005102 CRISPR transduction of iPS cells Other
2021-03-08
EGAS00001005104 Genetic landscape of inherited retinal dystrophies affected cases in Spain Other
2021-03-09
EGAS00001005106 Comparative transcriptome of CD34+ hematopoietic progenitors from myeloproliferative patients and control donors Other
2021-03-09
EGAS00001005107 Chronic myelomonocytic leukemia Other
2021-03-10
EGAS00001005108 Integrated genomic analysis identifies driver genes and cisplatin-resistant progenitor phenotype in pediatric liver cancer Other
2021-03-10
EGAS00001005109 Sequencing of cancer autopsies and ctDNA Other
2021-03-10
EGAS00001005110 International Genetics of Parkinson Disease Progression (IGPP) Consortium GWAS Summary Results Other
2021-03-10
EGAS00001005111 IG-MYC rearrangement defines a high-risk subgroup of B-cell precursor acute lymphoblastic leukaemia Cancer Genomics
2021-03-11
EGAS00001005112 The INFORM Precision Medicine Study for High-Risk Pediatric Malignancies Cancer Genomics
2021-03-11
EGAS00001005115 Cryopreservation of human cancers conserves tumour heterogeneity for single-cell multi-omics analysis Transcriptome Analysis
2021-03-12
EGAS00001005116 WES of clonally related neuroblastoma and teratoma Other
2021-03-13
EGAS00001005117 Whole-exome sequencing performed on a patient with chronic myelomonocytic leukemia and B cell acute lymphoblastic leukemia Other
2021-03-14
EGAS00001005118 Identification of novel colorectal cancer predisposition genes Cancer Genomics
2021-03-15
EGAS00001005121 ATAC-seq of uncultured CD112high and CD112low long-term(LT) human hematopoietic stem cells (HSC) from umbilical cord blood Other
2021-03-15
EGAS00001005125 Copy number analysis by SNP array Other
2021-03-16
EGAS00001005127 Accurate detection and classification of pediatric sarcomas based on cell-free DNA fragmentation patterns Other
2021-03-17
EGAS00001005128 Multiregional sequencing of IDH-WT glioblastoma reveals high genetic heterogeneity and a dynamic evolutionary history Other
2021-03-17
EGAS00001005130 RNA-Seq of vocal fold fibroblasts in Reinke’s edema and control subjects Other
2021-03-17
EGAS00001005132 Epigenomic profiling and transcriptomic profiling of LUAD patients tumor tissues and tumor adjacent tissues Other
2021-03-18
EGAS00001005134 Engineering large chromosomal deletions by CRISPR-Cas9 Other
2021-03-19
EGAS00001005137 Characterization of human iPSC-derived dopaminergic neurons with 16p11.2 CNVs Transcriptome Analysis
2021-03-22
EGAS00001005138 Increased trunk fat is associated with altered gene expression in breast tissue of normal weight women Transcriptome Analysis
2021-03-22
EGAS00001005140 Mixed Histology Lung Cancers Driven by Transcriptomic Features rather than Genomic Characteristics Cancer Genomics
2021-03-22
EGAS00001005141 Chemotherapy accelerates genomic aging of normal blood in children treated for cancer Other
2021-03-23
EGAS00001005144 Single cell RNA sequencing of synovial B cells in early Rheumatoid Arthritis Other
2021-03-24
EGAS00001005145 H021-Master Umbrella study2 (not to be released) Cancer Genomics
2021-03-24
EGAS00001005147 Assessment of the Toll-like receptor 3 response in hepatocytes Other
2021-03-25
EGAS00001005151 Single-cell transcriptome of human fetal pancreas and in vitro pancreatic spheroids Other
2021-03-25
EGAS00001005159 WGS bam Other
2021-03-28
EGAS00001005160 WES bam Other
2021-03-28
EGAS00001005161 RNA-seq bam Other
2021-03-28
EGAS00001005171 Genotype data from 'Evidence of the interplay of genetics and culture in Ethiopia' Other
2021-03-30
EGAS00001005173 An integrated multi-omic cellular atlas of human breast cancers RNASeq
2021-03-31
EGAS00001005174 sn-RNAseq profiling of the impact of a cytokine storm model in human cardiac organoids Other
2021-04-01
EGAS00001005178 Single-cell analysis of retinoblastoma heterogeneity RNASeq
2021-04-01
EGAS00001005180 Degradation of Janus kinases in CRLF2-rearranged acute lymphoblastic leukemia Other
2021-04-02
EGAS00001005181 G3BP2-KIT drives leukemia amenable to kinase inhibition in Ph-like ALL Other
2021-04-02
EGAS00001005182 Pediatric Papillary Thyroid Carcinoma RNA-Seq Other
2021-04-06
EGAS00001005187 Pediatric Papillary Thyroid Carcinoma Whole Exome Sequencing Other
2021-04-07
EGAS00001005188 Platelet response in aspirin adherent pregnant women Other
2021-04-07
EGAS00001005189 Nasal DNA methylation at three CpG sites predicts childhood allergic disease Epigenetics
2021-04-07
EGAS00001005194 Single cell and plasma RNA sequencing Other
2021-04-09
EGAS00001005196 Whole genome sequence and RNA-seq data from paired tumour and germline samples from mesothelioma patients. Other
2021-04-12
EGAS00001005197 arrayCGH for copy number profiling on tumor DNA from pediatric cancer tissue samples Other
2021-04-12
EGAS00001005198 sWGS on cfDNA and matching tumor DNA in pediatric cancer Other
2021-04-12
EGAS00001005199 Paired exome and low-coverage genome sequencing of osteosarcoma Other
2021-04-12
EGAS00001005201 The T cell receptor repertoire of tumor infiltrating T cells is predictive and prognostic for cancer survival Other
2021-04-12
EGAS00001005202 mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase Other
2021-04-12
EGAS00001005203 The distinct DNA methylome of acute lymphoblastic leukemia Other
2021-04-14
EGAS00001005204 Dissecting the Spatial Heterogeneity of Single Circulating Tumor Cells in Hepatocellular Carcinoma Other
2021-04-15
EGAS00001005205 Whole-Exome Sequences from Imazighen and non-Imazghen from Tunisia Other
2021-04-15
EGAS00001005206 High titers and low fucosylation of early phase anti-SARS-CoV-2 IgG promote hyper-inflammation by alveolar macrophages Other
2021-04-15
EGAS00001005214 Sclerosing epithelioid fibrosarcoma case report Other
2021-04-15
EGAS00001005215 Sclerosing epithelioid fibrosarcoma case report Other
2021-04-15
EGAS00001005220 Novel optineurin frameshift insertion causing familial frontotemporal dementia and parkinsonism without amyotrophic lateral sclerosis Other
2021-04-16
EGAS00001005221 Molecular characterization of Barrett’s esophagus at single cell resolution Other
2021-04-16
EGAS00001005222 Molecular characterization of hepatocellular carcinoma in patients with non-alcoholic steatohepatitis Other
2021-04-16
EGAS00001005224 Esophageal Adenocarcinoma Organoid Genomics Other
2021-04-16
EGAS00001005225 Gluten-free microbiome study UMCG Metagenomics
2021-04-18
EGAS00001005226 Splicing patterns in SF3B1 mutated uveal melanoma generate shared immunogenic tumor-specific neo-epitopes Other
2021-04-19
EGAS00001005227 Single-cell landscapes of primary glioblastomas and matched organoids and cell lines reveal variable retention of inter- and intra-tumor heterogeneity Other
2021-04-20
EGAS00001005228 Circulating tumor cells Exome sequencing from breast cancer Other
2021-04-21
EGAS00001005229 Improved Sezary cell detection and novel insights into immunophenotypic and molecular heterogeneity in Sézary syndrome Other
2021-04-22
EGAS00001005230 The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin. Other
2021-04-22
EGAS00001005232 Male-biased migration from East Africa introduced pastoralism into southern Africa Population Genomics
2021-04-23
EGAS00001005234 The evolution of hematopoietic cells under cancer therapy Other
2021-04-25
EGAS00001005235 Non-coding mutations reveal cancer driver cistromes in luminal breast cancer Other
2021-04-25
EGAS00001005237 Whole-genome landscape of adult T-cell leukemia/lymphoma Other
2021-04-26
EGAS00001005238 Targeted sequencing of follicular lymphoma tumour samples from the UK's Haematological Malignancy Research Network Other
2021-04-26
EGAS00001005241 Single cell sequencing reveals expanded cytotoxic CD4+ T cells and two clusters of peripheral helper T cells in synovial fluid of ACPA+ RA patients RNASeq
2021-04-26
EGAS00001005242 Evolutionary trajectories and clonal migration underlying tumor progression and lymph node metastasis in resectable lung cancer Cancer Genomics
2021-04-27
EGAS00001005243 Radiation-induced gliomas represent H3-/IDH-wild type pediatric gliomas with recurrent PDGFRA amplification and loss of CDKN2A/B Other
2021-04-27
EGAS00001005244 The_Little_Princess_Knowledge_Bank_RNAseq Other
2021-04-27
EGAS00001005245 Host genetic determinants of HIV infection Other
2021-04-27
EGAS00001005248 Genomic characterization of retinoblastoma Cancer Genomics
2021-04-27
EGAS00001005250 The genomic landscape of pediatric acute lymphoblastic leukemia Other
2021-04-29
EGAS00001005253 Combining a Universal Telomerase Based Cancer Vaccine with Ipilimumab in Patients with Metastatic Melanoma - Five-year Follow up of a Phase I/IIa Trial Other
2021-05-03
EGAS00001005254 Identification and functional characterisation of a rare MTTP variant underlying familial non-alcoholic fatty liver disease Other
2021-05-03
EGAS00001005255 Comparison of capture-based method for transcriptome profiling of formalin-fixed paraffin embedded tumor samples Other
2021-05-03
EGAS00001005256 Whole genome sequencing of adult glioblastoma nuclei Other
2021-05-03
EGAS00001005257 Single-cell RNA sequencing of 6 follicular lymphoma tumors Other
2021-05-04
EGAS00001005258 CD27hiCD38hi plasmablasts are activated B cells of mixed origin with distinct function Other
2021-05-04
EGAS00001005263 The Extracellular RNA Quality Control (exRNAQC) study (phase 1) RNASeq
2021-05-05
EGAS00001005268 Characterizing microbiome-directed fibre snacks in gnotobiotic mice and humans Other
2021-05-05
EGAS00001005270 Molecular characteristics in Burkitt lymphoma over age groups Other
2021-05-06
EGAS00001005271 Human Inflammatory Skin Disease scRNA-seq RNASeq
2021-05-06
EGAS00001005273 Exome_sequencing_of_UK_Birth_Cohorts___Avon_Longitudinal_Study_of_Parents_and_Children Other
2021-05-07
EGAS00001005274 Prediction of HLA genotypes using NGS data Other
2021-05-07
EGAS00001005276 Genomic and Transcriptomic Profile of Paired Primary-Metastasis Colorectal Tumors Other
2021-05-07
EGAS00001005277 Extracellular transcriptome in seminal plasma for non-invasive prostate cancer diagnosis Other
2021-05-10
EGAS00001005280 Impaired Humoral and Cellular Immunity after SARS-CoV2 BNT162b2 (Tozinameran) Prime-Boost Vaccination in Kidney Transplant Recipients RNASeq
2021-05-10
EGAS00001005281 ATAC-seq data in normal colon mucosa Other
2021-05-11
EGAS00001005286 Hypoxia acts as an environmental cue for the human TRM differentiation program Other
2021-05-11
EGAS00001005295 atrial appendage RNA-seq in non-, paroxysmal and persistent atrial fibrillation Other
2021-05-12
EGAS00001005297 Single-cell profiling of the leukemic and non-leukemic immune cell compartments in CD8+ T-cell Large Granular Lymphocytic Leukemia Other
2021-05-12
EGAS00001005298 HSC_colony_many_years_post_allogeneic_bone_marrow_transplant_TGS Other
2021-05-12
EGAS00001005299 ALLoreactive T-Cell receptOr RePertoire in kidnEy tranSplantation Other
2021-05-14
EGAS00001005300 Multimodal single-cell and bulk glioma analyses Other
2021-05-15
EGAS00001005301 Circulating tumor cell copy-number heterogeneity in ALK-rearranged non-small-cell lung cancer resistant to ALK inhibitors Other
2021-05-15
EGAS00001005303 ChIP-seq in colorectal cancer and paired adjacent normal mucosa Other
2021-05-17
EGAS00001005304 COVID19 Host Genetic Initiative Other
2021-05-17
EGAS00001005305 Bulk-tissue RNA-sequencing of anterior cingulate cortex samples derived from Lewy body disease patients Other
2021-05-18
EGAS00001005312 Genomic Rearrangements in Pediatric Cancer Other
2021-05-19
EGAS00001005313 Genomic Analysis of Focal Nodular Hyperplasia with Associated Hepatocellular Carcinoma Unveils its Malignant Potential Cancer Genomics
2021-05-19
EGAS00001005314 Evolutionary predictability of genetic versus non genetic resistance to anticancer drugs in melanoma Other
2021-05-19
EGAS00001005315 Genome-wide data from Agta hunter-gatherers in Philippines Other
2021-05-19
EGAS00001005317 Oral microbiome composition of Agta hunter-gatherers (16S) Other
2021-05-19
EGAS00001005319 Microbiota, Appetite, and Malnutrition in Dutch Community-dwelling older adults Metagenomics
2021-05-20
EGAS00001005320 Secondary Resistance to Anti-EGFR Therapy by Transcriptional Reprogramming in Patient-Derived Colorectal Cancer Models (hipo_B012) Cancer Genomics
2021-05-21
EGAS00001005321 Pediatric tumor in a single child of three large nuclear families Other
2021-05-21
EGAS00001005322 Neuroblastoma tumor heterogeneity and cell plasticity (from patients) Other
2021-05-25
EGAS00001005323 Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples Other
2021-05-25
EGAS00001005325 Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing - NGS targeted capture control cohort Other
2021-05-26
EGAS00001005326 Immune infiltrate and tumor microenvironment transcriptional programs stratify pediatric osteosarcoma into prognostic groups at diagnosis Transcriptome Analysis
2021-05-26
EGAS00001005327 Identification of early disease progression in ALK-rearranged lung cancer using circulating tumor DNA analysis (hipo_K34R) Cancer Genomics
2021-05-26
EGAS00001005328 Multi-site tumor sampling highlights molecular intra-tumor heterogeneity in malignant pleural mesothelioma Other
2021-05-26
EGAS00001005329 Exome Sequecning of MDS xenografted samples Other
2021-05-26
EGAS00001005330 An approach for evaluating the effects of dietary fiber polysaccharides on the human gut microbiome and plasma proteome Metagenomics
2021-05-27
EGAS00001005331 Correction of FFPE artefacts in WGS data Other
2021-05-27
EGAS00001005332 COVID-19 whole blood transcriptomic analysis RNASeq
2021-05-27
EGAS00001005339 The mutational landscape of primary central nervous system lymphoma (Hipo H050, A050, XD013) Other
2021-05-28
EGAS00001005340 Detection and characterization of lung cancer using cell-free DNA fragmentomes Other
2021-05-28
EGAS00001005341 WGS Leiomyosarcoma subtypes Whole Genome Sequencing
2021-05-28
EGAS00001005342 Metabolomic and microbiome profiling reveals personalized risk factors for coronary artery disease Other
2021-05-31
EGAS00001005343 Single-cell profiling of neoantigen-specific T cells in lung cancers treated with neoadjuvant PD-1 blockade Other
2021-06-01
EGAS00001005345 Whole genome sequencing based on short and long reads from GM09237 cell line with and without folate depletion Other
2021-06-01
EGAS00001005346 Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features Exome Sequencing
2021-06-01
EGAS00001005347 An instructive role for IL7RA in the development of human B-cell precursor leukemia Other
2021-06-01
EGAS00001005348 Integration of metabolomics, genomics and immune phenotypes reveals the causal roles of metabolites in disease Population Genomics
2021-06-01
EGAS00001005350 Human gut microbiome in babies with biliary atresia and normal controls Metagenomics
2021-06-01
EGAS00001005352 Efficacy of CDK4/6i in preclinical models of malignant pleural mesothelioma Other
2021-06-02
EGAS00001005354 The Xq22.3 contiguous gene deletion syndrome (ATS-ID) Exome Sequencing
2021-06-02
EGAS00001005355 Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features Cancer Genomics
2021-06-02
EGAS00001005356 Sequential single-cell transcriptional and protein marker profiling reveals TIGIT as a marker of CD19 CAR-T cell dysfunction in patients with non-Hodgkin’s lymphoma Other
2021-06-02
EGAS00001005357 The Xq22.3 contiguous gene deletion syndrome (ATS-ID): from genotype to further delineation of the phenotype Exome Sequencing
2021-06-02
EGAS00001005358 Evaluating CRISPR-based Prime Editing for cancer modeling and CFTR repair in organoids Whole Genome Sequencing
2021-06-03
EGAS00001005359 SmMIP-tools:a computational toolset for processing and analysis of single-molecule molecular inversion probes derived data Other
2021-06-03
EGAS00001005360 The genetic scenario of Mercheros: an under-represented population within the Iberian Peninsula Other
2021-06-03
EGAS00001005361 Nucleosome footprinting in plasma cell-free DNA for diagnosis of ovarian cancer Other
2021-06-04
EGAS00001005362 Settlement of Polynesia Other
2021-06-04
EGAS00001005363 Molecular profiles and urinary biomarkers of upper tract urothelial carcinomas associated with aristolochic acid exposure Other
2021-06-07
EGAS00001005364 Mongolia Western HCC Other
2021-06-07
EGAS00001005366 Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome Other
2021-06-07
EGAS00001005367 Whole-genome sequencing of lymphomas in immune-privileged sites Whole Genome Sequencing
2021-06-08
EGAS00001005368 RNA-seq on neuroblastoma PDX model COG-N-519 treated with control miR-1283 and test miR-99b-5p mimics RNASeq
2021-06-08
EGAS00001005369 Retinal Dystrophy_analysis Exome Sequencing
2021-06-08
EGAS00001005370 RNAseq from regions of insitu and invasive human mammary ductal disease RNASeq
2021-06-08
EGAS00001005372 Evidence that ciliary genes contribute to non-syndromic familial tall stature Exome Sequencing
2021-06-10
EGAS00001005373 Genes___Health_imputed_genotype_dataset Population Genomics
2021-06-10
EGAS00001005374 Transcriptome and epigenome characterization of BMP signaling effects on H3.3K27M DIPG Other
2021-06-11
EGAS00001005376 Single-cell RNA sequencing dissects gene-environment interactions on gene expression and regulation in immune cells. Other
2021-06-11
EGAS00001005377 Spatiotemporal single cell transcriptomic analysis of human gut macrophages reveals multiple functional and niche-specific subsets RNASeq
2021-06-11
EGAS00001005378 Placental microRNA sequencing data from human placenta RNASeq
2021-06-11
EGAS00001005379 SG Peranakan Project: Genetic admixture in the culturally unique Peranakan Chinese population in Southeast Asia Other
2021-06-11
EGAS00001005380 An analysis of humoral and cellular immune responses following COVID-19 vaccination. Other
2021-06-11
EGAS00001005382 Single cell copy number and chromatin accessibility in primary multiple myeloma cells Other
2021-06-11
EGAS00001005384 Mutational impact in liver stem cells under precancerous alcoholic liver, NASH and PSC disease conditions Whole Genome Sequencing
2021-06-14
EGAS00001005387 Alveolar Rhabdomyosarcoma sequencing data Other
2021-06-14
EGAS00001005389 Integrative Profiling of T790M Negative EGFR Mutated NSCLC Reveals Pervasive Lineage Transition and Therapeutic Opportunities Other
2021-06-15
EGAS00001005392 Evaluation of the immune effects of tumor-treating electric fields (TTFields) in GBM patients RNASeq
2021-06-16
EGAS00001005393 Papua New Guinean Genome Diversity Project Other
2021-06-16
EGAS00001005394 Functional dissection of inherited non-coding variation influencing multiple myeloma risk Other
2021-06-16
EGAS00001005395 Analysis of RAD51C promoter methylation using targeted bisulfite sequencing (amplicon sequencing) in ovarian cancer pre-clinical models and patient samples. Other
2021-06-17
EGAS00001005396 Interferon lambda 4 impairs viral antigen presentation and attenuates T cell responses Other
2021-06-17
EGAS00001005398 Prevalence of transthyretin amyloidosis in patients with heart failure and no left ventricular hypertrophy Other
2021-06-17
EGAS00001005399 PELICAN33 longitudinal clinical and autopsy phenomic assessment in lethal metastatic prostate cancer Other
2021-06-17
EGAS00001005401 Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing Other
2021-06-18
EGAS00001005402 Genomic characterization of co-existing biliary tract intraepithelial neoplasia and carcinoma lesions reveals distinct evolutionary paths of gallbladder cancer Other
2021-06-21
EGAS00001005403 Germline RUNX1 Variation and Predisposition to Childhood Acute Lymphoblastic Other
2021-06-21
EGAS00001005405 Identifying transcriptional programs underlying anti-EGFR small molecule response and resistance with TraCe-seq Other
2021-06-21
EGAS00001005407 Philippine Ayta possess the highest level of Denisovan ancestry in the world Other
2021-06-22
EGAS00001005408 Philippine Ayta possess the highest level of Denisovan ancestry in the world Other
2021-06-22
EGAS00001005411 Genotyping by OncoArray and Global Screening Array for colorectal cancer risk prediction Other
2021-06-22
EGAS00001005412 NSCCG CRC GWAS data Other
2021-06-22
EGAS00001005414 Adult-type Granulosa Cell Tumour of the Ovary Other
2021-06-22
EGAS00001005417 Genetics causes of male infertility in 185 patient-parent trios from Netherlands and UK Other
2021-06-24
EGAS00001005418 Custom long non-coding RNA capture enhances detection sensitivity in different human sample types. Other
2021-06-28
EGAS00001005419 Molecular profile of IMFT for the identification of potential druggable targets and biomarkers predicting crizotinib response. Other
2021-06-28
EGAS00001005420 Mutational landscape of high-grade B-cell lymphoma with MYC-, BCL2 and/or BCL6 rearrangements characterized by whole-exome sequencing Other
2021-06-28
EGAS00001005421 COIN CRC GWAS data Other
2021-06-28
EGAS00001005422 Integration of genomics and metabolomics in acute myeloid leukemia Other
2021-06-28
EGAS00001005423 ANGIOPREDICT - an FP7-funded project enabling personalised medicine for patients with metastatic colorectal cancer. Other
2021-06-29
EGAS00001005424 Chromothripsis followed by circular recombination drives oncogene amplification in human cancer Other
2021-06-29
EGAS00001005426 Sequence Data from the phase 2 PrE0505 trial of Durvalumab with First Line Platinum-Pemetrexed for Unresectable Pleural Mesothelioma Other
2021-06-30
EGAS00001005429 WES on tumor DNA and germline DNA in pediatric cancer Other
2021-07-01
EGAS00001005430 Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System Other
2021-07-01
EGAS00001005431 Targeted deep sequencing on Pediatric MDS Other
2021-07-01
EGAS00001005432 Whole exome sequencing on Pediatric MDS patients Other
2021-07-01
EGAS00001005433 Single-cell DNA sequencing on Pediatric MDS Other
2021-07-01
EGAS00001005434 Spatial concordance of DNA methylation classification in diffuse glioma Other
2021-07-01
EGAS00001005435 Risk alleles of membranous nephropathy and recurrence of the disease on the grafted kidney Other
2021-07-02
EGAS00001005436 G-SAM: Transcriptional Evolution of Glioblastomas Treated With Standard of Care Other
2021-07-02
EGAS00001005437 Intellance-2: omics data on recurrent glioblastoma patients participating in the Intellance-2 clinical trial, prior to treatment. Other
2021-07-02
EGAS00001005442 Whole exome sequencing (bam files) of 55 samples of myxofibrosarcoma and 44 matched pairs Other
2021-07-05
EGAS00001005443 Targeted-capture sequencing (bam files) of 81 samples of myxofibrosarcoma and 44 matched pairs Other
2021-07-05
EGAS00001005444 Whole genome sequencing (bam files) of 5 samples of myxofibrosarcoma and 5 matched pairs Other
2021-07-05
EGAS00001005446 Induction of trained immunity by influenza vaccine: impact on COVID-19 RNASeq
2021-07-05
EGAS00001005448 SMARCA4/2 loss inhibits chemotherapy-induced apoptosis by restricting IP3R3-mediated Ca2+ flux to mitochondria RNASeq
2021-07-06
EGAS00001005450 MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__head___neck Other
2021-07-06
EGAS00001005453 Predictive value of chromosome 18q11.2-q12.1 loss for benefit from bevacizumab in metastatic colorectal cancer; a post-hoc analysis of the randomized controlled trial AGITG-MAX Other
2021-07-06
EGAS00001005454 IMCISION RNAseq Other
2021-07-07
EGAS00001005455 Misoprostol-induced high fever GWAS study Other
2021-07-07
EGAS00001005457 KIR gene content imputation from single-nucleotide polymorphisms in the Finnish population Other
2021-07-11
EGAS00001005458 A body map of somatic mutagenesis in morphologically normal human tissues (WGS) Whole Genome Sequencing
2021-07-12
EGAS00001005459 A body map of somatic mutagenesis in morphologically normal human tissues (WES) Exome Sequencing
2021-07-12
EGAS00001005461 Pre-activated anti-viral innate immunity in the upper airways controls early SARS-CoV-2 infection in children Other
2021-07-12
EGAS00001005462 ChIP-Seq of TFEB in LT-HSC Other
2021-07-12
EGAS00001005464 Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia - Acute myeloid leukemia Other
2021-07-13
EGAS00001005465 Multi-omic single-cell profiling of peripheral blood immune cells from COVID-19 patients and controls. Other
2021-07-14
EGAS00001005466 IMCISION DNAseq Other
2021-07-15
EGAS00001005468 An epigenomics time course analysis of covid19 patients from Quebec, Canada Other
2021-07-16
EGAS00001005470 Genome sequencing of childhood acute leukemia in Iraq Other
2021-07-19
EGAS00001005472 Epigenetic encoding, heritability and plasticity of glioma transcriptional cell states Cancer Genomics
2021-07-20
EGAS00001005475 Sequence data for study: Mobilization of tissue-resident memory CD4+ T lymphocytes from bone marrow and their contribution to a systemic secondary immune reaction Other
2021-07-21
EGAS00001005476 TULIPs decorate the three-dimensional genome of PFA ependymoma Epigenetics
2021-07-22
EGAS00001005477 Microarray Markers of Response Transcriptome Analysis
2021-07-22
EGAS00001005478 The PEMDAC phase 2 study of pembrolizumab and entinostat in patients with metastatic uveal melanoma Other
2021-07-23
EGAS00001005479 Multi-omics analysis of serial samples from metastatic TNBC patients on PARP inhibitor monotherapy provide insight into rational PARP inhibitor therapy combinations Other
2021-07-23
EGAS00001005480 Analysis of T-cell receptor clonotypes in tumor micro-environment identifies shared cancer type-specific signatures Other
2021-07-26
EGAS00001005482 Non-small cell lung cancer proteome subtypes expose targetable oncogenic drivers and immune evasion mechanisms Other
2021-07-26
EGAS00001005488 MM.1S Single Cell Multiome (ATAC + Gene Expression) Population Genomics
2021-07-27
EGAS00001005493 A blood atlas of COVID-19 defines hallmarks of disease severity and specificity Other
2021-07-27
EGAS00001005495 Multi-omics of Richter syndrome Other
2021-07-27
EGAS00001005496 Correction of a Factor VIII genomic inversion with designer recombinases Other
2021-07-27
EGAS00001005498 Unraveling the transcriptomic profile of utero-tubal lavage fluid of ovarian cancer patients Other
2021-07-28
EGAS00001005499 Non-small cell lung cancer sequencing Cancer Genomics
2021-07-28
EGAS00001005501 CM214 - Biomarker Analysis From the Phase 3 CheckMate 214 Trial of Nivolumab Plus Ipilimumab (N+I) or Sunitinib (S) in Advanced Renal Cell Carcinoma (aRCC) Other
2021-07-29
EGAS00001005502 Embryonal Rhabdomyosarcoma sequencing data Other
2021-07-29
EGAS00001005503 Integrated genomic analyses reveal molecular correlates of clinical response and resistance to atezolizumab in combination with bevacizumab in advanced hepatocellular carcinoma Other
2021-07-30
EGAS00001005507 Single Cell Transcriptomics of peripheral immune cells pre- and post-Immune Checkpoint Blockade RNASeq
2021-07-30
EGAS00001005508 Role of cohesin/CTCF in human monocyte differentiation Other
2021-07-30
EGAS00001005509 A Single-cell Atlas of Progressive TKI Resistance in Chronic Myeloid Leukemia Other
2021-07-30
EGAS00001005511 Integrated Exome-seq analysis of tumor thrombus Other
2021-07-30
EGAS00001005512 Integrated RNA-seq analysis of tumor thrombus Other
2021-07-30
EGAS00001005513 Cancer and germline exomes, and cancer RNA-seq consisiting of FASTQ paired-end reads from melanoma, lung and colon cancer samples Other
2021-08-02
EGAS00001005514 Methylation clocks - individual colon, small intestine and endometrial crypts Epigenetics
2021-08-03
EGAS00001005515 Long cell-free DNA molecules in maternal plasma Other
2021-08-03
EGAS00001005516 A renal cell carcinoma tumorgraft platform to advance precision medicine Cancer Genomics
2021-08-03
EGAS00001005517 Differential expression profile of gluten-specific T cells identified by single-cell RNA-seq Other
2021-08-04
EGAS00001005518 PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysm in humans Other
2021-08-04
EGAS00001005520 Immune profiling reveals enrichment of distinct immune signatures in high-risk oral potentially malignant disorders Other
2021-08-05
EGAS00001005522 The cell free DNA methylome of primary and metastatic prostate tumors Other
2021-08-05
EGAS00001005523 Pearl study Cancer Genomics
2021-08-06
EGAS00001005524 Dynamic N6-methyladenosine Epitranscriptomic Landscape in Lung Adenocarcinoma Other
2021-08-06
EGAS00001005525 Alterations in the gut microbiome in inflammatory arthritis implicate key taxa and metabolic pathways across arthritis phenotypes Metagenomics
2021-08-06
EGAS00001005528 CRISPR_single_cell_activation Other
2021-08-09
EGAS00001005529 Multi-omics integration reveals only minor long-term molecular and functional sequelae in immune cells of individuals recovered from COVID-19 Other
2021-08-09
EGAS00001005530 Pathogenic Neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq Other
2021-08-09
EGAS00001005532 PAH sequencing study Other
2021-08-09
EGAS00001005533 SJCRH Patient-derived orthotopic xenografts of pediatric brain tumors Other
2021-08-09
EGAS00001005534 HSC_colony_many_years_post_allogeneic_bone_marrow_transplant___Bait_set_2 Other
2021-08-11
EGAS00001005535 Pancreatic islets PISA RNA-seq samples Other
2021-08-13
EGAS00001005536 Transcriptome Changes in ASD (NRXN1α+/-) iPSC-derived neurons Other
2021-08-13
EGAS00001005537 Germline variants in patients with rare cancers and their implications for precision cancer medicine: experiences from the Multicenter MASTER Trial by the German Cancer Consortium (HIPO_021) Other
2021-08-13
EGAS00001005539 Clonal dynamics of normal hepatocyte expansions in homeostatic human livers and their association with the biliary epithelium Whole Genome Sequencing
2021-08-13
EGAS00001005540 Mitochondrial DNA sequencing Cancer Genomics
2021-08-15
EGAS00001005541 Single-cell RNA-seq data of the tumor microenvironment of lymphocyte-rich Hodgkin lymphoma and other Hodgkin lymphoma subtypes Other
2021-08-16
EGAS00001005543 Multipolar zygotic divisions are characterized by parental genome segregation errors Other
2021-08-17
EGAS00001005544 Investigation of the keratinocytic gene expression pattern in Hidradenitis suppurativa Other
2021-08-18
EGAS00001005545 Longitudinal Single Cell Atlas of COVID-19 Identifies an Early, Transient Prognostic Signature Transcriptome Analysis
2021-08-18
EGAS00001005546 Minor intron splicing efficiency increases with the development of lethal prostate cancer Transcriptome Analysis
2021-08-19
EGAS00001005549 Expression-Based Subtypes Define Pathologic Response to Neoadjuvant Immune-Checkpoint Inhibitors in Muscle-Invasive Bladder Cancer Other
2021-08-19
EGAS00001005550 Genomic characterization of retinoblastoma (targeted sequencing) Other
2021-08-19
EGAS00001005553 Pediatric study using genome sequencing Other
2021-08-20
EGAS00001005554 DLBCL NGS Genomic Datasets of non-China cohort from Phoenix Clinical Trial Other
2021-08-22
EGAS00001005556 Automated machine-learning approach for next generation profiling of sequence alterations, mutation burden, microsatellite instability, and structural variants in human cancers Other
2021-08-24
EGAS00001005558 Whole-transcriptome sequencing of hepatocellular carcinoma biopsies (TACE study) Other
2021-08-24
EGAS00001005559 WGS_of_healhy_mesothelial_cells_and_primary_mesothelima_cell_lines Other
2021-08-24
EGAS00001005560 Mitochondrial DNA sequencing of iPSC, parental cells, and iPSC derived cardiomyocytes Other
2021-08-26
EGAS00001005561 Genomic profiling of Follicular thyroid adenomas and carcinomas using exome-sequencing analyses Other
2021-08-26
EGAS00001005562 Jagged ends of plasma DNA (human) Other
2021-08-27
EGAS00001005563 Jagged ends of plasma DNA (mouse) Other
2021-08-27
EGAS00001005565 Transcriptomes of human CD4+ T lymphocytes - Metabolic project Other
2021-08-27
EGAS00001005567 The genomic landscape of early stage ovarian high grade serous carcinoma Whole Genome Sequencing
2021-08-27
EGAS00001005569 Are children born after medical assisted reproduction at greater risk of having an increased de novo mutation rate? Other
2021-08-31
EGAS00001005572 Whole genome sequencing of a breast cancer cohort with known functional homologous recombination status Other
2021-09-01
EGAS00001005573 Expression signatures of NGLY1 deficiency RNASeq
2021-09-01
EGAS00001005577 Spatial Deconvolution of HER2-positive Breast Tumors Transcriptome Analysis
2021-09-02
EGAS00001005579 Mutation and Microsatellite Burden Predict Response to PD-1 Inhibition in Children with Germline DNA Replication Repair Deficiency: An Observational Registry Study Cancer Genomics
2021-09-03
EGAS00001005580 Single-cell characterization of anti-LAG3+anti-PD1 treatment in melanoma patients Other
2021-09-03
EGAS00001005581 RNA-seq on neuroblastoma PDX model COG-N-519 treated with control miR-1283 and test miR-99b-5p mimics Other
2021-09-04
EGAS00001005582 T cell receptors of pathogenic CD4 T cells isolated by using distinct phenotypic markers in celiac disease Other
2021-09-05
EGAS00001005583 46 patients primary malignant glioma cohort in Chinese population Other
2021-09-06
EGAS00001005584 Genomics to select patients with metastatic breast cancer for targeted therapy (microarray_cytoscan) Other
2021-09-06
EGAS00001005586 Genomics to select patients with metastatic breast cancer for targeted therapy (microarray_oncoscan) Other
2021-09-06
EGAS00001005587 Genomics to select patients with metastatic breast cancer for targeted therapy (microarray_agilent) Other
2021-09-06
EGAS00001005588 RNA-sequencing of tumors from 45 patients with recurrent or metastatic gastric cancer treated with immune checkpoint inhibitors Other
2021-09-06
EGAS00001005589 Benchmarking DIA-type Proteomics Using Large-Scale Inter-Patient Heterogeneity Dataset Other
2021-09-06
EGAS00001005591 Synthetic data - Genome in a Bottle Other
2021-09-07
EGAS00001005592 Serial assessment of measurable residual disease in medulloblastoma liquid biopsies Other
2021-09-07
EGAS00001005593 Single-cell proteo-genomic reference maps of the human hematopoietic system Other
2021-09-09
EGAS00001005594 Myeloid cell programming in patients with non-medullary thyroid carcinoma RNASeq
2021-09-09
EGAS00001005596 Genetics and therapeutic responses to TIL therapy of pancreatic cancer PDX models Other
2021-09-10
EGAS00001005597 Patient data used in FLTseq paper Other
2021-09-12
EGAS00001005599 Human skeletal muscle CD90+ fibro-adipogenic progenitors are associated with muscle degeneration in type 2 diabetic patients Transcriptome Analysis
2021-09-13
EGAS00001005600 Osteosarcoma sequencing data Other
2021-09-13
EGAS00001005601 Absolute copy number fitting from shallow whole genome sequencing data Whole Genome Sequencing
2021-09-13
EGAS00001005602 Neuroblastoma sequencing data Other
2021-09-13
EGAS00001005603 High-resolution analysis for urinary DNA jagged ends Other
2021-09-14
EGAS00001005604 Berlin Neuroblastoma Dataset Update 2021 Cancer Genomics
2021-09-14
EGAS00001005605 Application of Hi-C sequencing to detect structural variants in B-cell acute lymphoblastic leukemia Other
2021-09-14
EGAS00001005606 SNP array study in Autism Spectrum Disorder patients Other
2021-09-16
EGAS00001005610 WGBS and oxBS-seq for APL Whole Genome Sequencing
2021-09-18
EGAS00001005612 Transcriptomic consequences of complex rearrangements inv8p23.1 and inv17q21.31 associated with Autism Spectrum Disorders Other
2021-09-20
EGAS00001005613 APL Oxford Nanopore sequencing - nanome Whole Genome Sequencing
2021-09-20
EGAS00001005615 Pediatric B-cell precursor acute lymphoblastic leukemia samples with very early relapse Other
2021-09-21
EGAS00001005616 Combined Metabolic Activators Reduces Liver Fat in Nonalcoholic Fatty Liver Disease Patients Other
2021-09-21
EGAS00001005617 Genomic abnormalities of TP53 define distinct risk groups of paediatric B-cell non-Hodgkin lymphoma Other
2021-09-21
EGAS00001005618 APL nanopore sequencing Other
2021-09-21
EGAS00001005619 IVF Whole genome prediction Other
2021-09-21
EGAS00001005620 Multifocal ileal NETs study WGS normal tissue Whole Genome Sequencing
2021-09-22
EGAS00001005621 Multifocal ileal NETs study WGS HF3J5CCXY Whole Genome Sequencing
2021-09-22
EGAS00001005622 Multifocal ileal NETs study WGS HF3FKCCXY Whole Genome Sequencing
2021-09-22
EGAS00001005623 Multifocal ileal NETs study WGS HFG3FCCXY Whole Genome Sequencing
2021-09-22
EGAS00001005624 Multifocal ileal NETs study WGS HF3NYCCXY Whole Genome Sequencing
2021-09-22
EGAS00001005625 Multifocal ileal NETs study WGS HFFWLCCXY Whole Genome Sequencing
2021-09-22
EGAS00001005626 Matched tissue from BRCA1/2 mutation carriers and confirmed non-BRCA mutation carriers Other
2021-09-23
EGAS00001005627 A microRNA-signature that correlates with cognition and is a target against cognitive decline Other
2021-09-23
EGAS00001005629 Whole genome sequencing data for 10 hepatocellular carcinomas (HCC) and matched non-tumor liver tissues + optical mapping data for 4 HCC and 3 matched non-tumor liver tissues. Other
2021-09-24
EGAS00001005632 Genomic Signatures Define Three Subtypes of EGFR-Mutant Stage II-III NSCLC With Distinct Adjuvant Therapy Outcomes Cancer Genomics
2021-09-28
EGAS00001005633 scRNAseq of human primary nasal epithelium differentiated at air-liquid interface exposed to SARS-CoV2 Other
2021-09-28
EGAS00001005634 Single-cell RNA-seq of bronchoalveolar lavage (BAL) fluid of late stage severe COVID-19 patients Other
2021-09-29
EGAS00001005637 ADAPTeR Study: RNAseq data from ccRCC patients Other
2021-09-30
EGAS00001005638 ADAPTeR Study: WES data from ccRCC patients Other
2021-09-30
EGAS00001005639 ADAPTeR Study: TCRseq data from ccRCC patients Other
2021-09-30
EGAS00001005640 ADAPTeR Study: scRNA and scTCR data from TILs from two ccRCC patients treated with anti-PD1 Other
2021-09-30
EGAS00001005641 Proteom characterization in primary colorectal cancer and corresponding liver metastasis Other
2021-10-01
EGAS00001005642 Paediatric_CNS_tumour_autopsy_DNA_WES Other
2021-10-01
EGAS00001005647 Multi-omic Profiling of Central Nervous System Leukemia Identifies mRNA Translation as a Therapeutic Target Other
2021-10-01
EGAS00001005648 The genomic landscape of serrated lesion of the colorectum Other
2021-10-04
EGAS00001005649 Variation and transmission of the human gut microbiota across generations - shotgun data Other
2021-10-04
EGAS00001005651 Variation and transmission of the human gut microbiota across generations - 16S data Other
2021-10-04
EGAS00001005653 PIK3CA mutation in a case of CTNNB1 mutant sinonasal glomangiopericytoma Exome Sequencing
2021-10-04
EGAS00001005655 RNAseq in blood CD34+ cells Other
2021-10-05
EGAS00001005656 Pre-neoplastic somatic mutations including MYD88L265P in lymphoplasmacytic lymphoma Other
2021-10-06
EGAS00001005661 Whole-exome sequencing of HCC patients undergoing sorafenib treatment Other
2021-10-06
EGAS00001005662 RNA-sequencing of HCC patients undergoing sorafenib treatment Other
2021-10-06
EGAS00001005665 DGCR8 and the six hit, three-step model of schwannomatosis Other
2021-10-07
EGAS00001005667 Surgery in combination with immune checkpoint therapy as an effective treatment for patients with metastatic cancer. Exome Sequencing
2021-10-08
EGAS00001005669 SudanMitoSeq: Sudanese mitochondrial sequencing Other
2021-10-13
EGAS00001005673 Whole exome sequencing of Congenital Cataract Other
2021-10-15
EGAS00001005675 Germline biallelic mutation affecting the transcription factor Helios causes pleiotropic defects of immunity Other
2021-10-15
EGAS00001005676 Identification of biomarkers of response to preoperative talazoparib monotherapy in treatment naïve gBRCA+ breast cancers Other
2021-10-18
EGAS00001005677 Small variants in mtDNA Canary Islands - WGS Oxford Nanopore Technologies (ITER) Other
2021-10-18
EGAS00001005678 Small variants in mtDNA Canary Islands - WES Illumina (ITER) Other
2021-10-18
EGAS00001005679 Small variants in mtDNA Canary Islands - WGS Illumina (ITER) Other
2021-10-18
EGAS00001005680 Targeted sequencing of candidate regions on chromosome 22q predisposing to multiple schwannomas Other
2021-10-18
EGAS00001005681 Disturbed trophoblast transition links early fetal to maternal syndrome progression in pre-eclampsia Transcriptome Analysis
2021-10-18
EGAS00001005684 MM samples for epigenomic translocation of H3K4me3 broad domains following super-enhancer hijacking Other
2021-10-18
EGAS00001005685 Whole Exome Sequencing of Localized Prostate Cancer Patients Other
2021-10-18
EGAS00001005686 MNM - Temporal variability in Quantitative Microbiome Profiles Other
2021-10-18
EGAS00001005687 Pediatric HGG WES and RNA-Seq Other
2021-10-19
EGAS00001005689 Ewing's sarcoma sequencing data Other
2021-10-19
EGAS00001005690 Wilm's tumor sequencing data Other
2021-10-19
EGAS00001005691 Single-nucleus transcriptomic profiling of aging Down Syndrome brains Other
2021-10-19
EGAS00001005692 Signals of positive selection in Peruvians from three ecological regions Other
2021-10-19
EGAS00001005696 COVID_19_Challenge_Project_Single_Cell_Profiling Other
2021-10-21
EGAS00001005697 Single-cell RNA sequencing of a PBMC sample collected from a male with 45,X/48,XYYY karyotype Transcriptome Analysis
2021-10-21
EGAS00001005698 Somatic pathogenic variants in the normal mammary gland of sporadic breast cancer patients. Other
2021-10-21
EGAS00001005700 Genomic profile of sporadic multiple meningiomas Other
2021-10-21
EGAS00001005702 Human genomic and phenotypic synthetic data for the study of rare diseases Other
2021-10-22
EGAS00001005704 BARIA baseline first 100 individuals transcriptomes Other
2021-10-25
EGAS00001005720 DERMATLAS__Porocarcinoma_WES Other
2021-10-26
EGAS00001005721 DERMATLAS__Porocarcinoma_RNAseq Other
2021-10-26
EGAS00001005728 RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines Other
2021-10-26
EGAS00001005729 Barrett esophagus phenotypic evolution study Whole Genome Sequencing
2021-10-26
EGAS00001005730 Human and rat skeletal muscle multi-omic profiling Other
2021-10-26
EGAS00001005731 DNA methylation and Panel sequencing for pancreatic neuroendocrine carcinomas (PanNECs) and pancreatic neuroendocrine tumors (PanNETs) Cancer Genomics
2021-10-26
EGAS00001005732 scRNA-seq of LN and lymphoma stroma Other
2021-10-27
EGAS00001005734 Molecular_risk_stratification_in_patients_with_T1_colorectal_cancer_WES Other
2021-10-28
EGAS00001005735 Unifying recovery dynamics in heterogeneous diseases exemplified by COVID-19 Other
2021-10-28
EGAS00001005736 Mult-omics Palbociclib Resistance Study in HR+/HER2– Metastatic Breast Cancer Other
2021-10-29
EGAS00001005737 Genetic variability in exon 1 of the glucocorticoid receptor gene NR3C1 is associated with postoperative complications Other
2021-10-29
EGAS00001005738 Genome-wide cell-free DNA termini in patients with cancer Other
2021-10-29
EGAS00001005739 cfDNA and CDX/PDX methylation profiling in SCLC Other
2021-10-29
EGAS00001005740 Whole transcriptome profiling of liquid biopsies from tumour xenografted mouse models enables specific monitoring of tumour-derived extracellular RNA RNASeq
2021-10-29
EGAS00001005743 Comparative analysis of RAF depletion vs. MAPK inhibition RNASeq
2021-10-29
EGAS00001005744 IN UTERO ORIGIN OF MYELOFIBROSIS PRESENTING IN ADULT MONOZYGOTIC TWINS AFTER A PROLONGED DISEASE LATENCY Cancer Genomics
2021-10-29
EGAS00001005745 Stereotyped B-cell responses are linked to IgG constant region polymorphisms in multiple sclerosis Other
2021-10-30
EGAS00001005746 Proteogenomics of chronic lymphocytic leukemia Other
2021-10-31
EGAS00001005747 Genome-wide cell-free DNA termini in patients with cancer Other
2021-11-01
EGAS00001005748 The effect of pre-analytical and physiological variables on cell-free DNA fragmentation Other
2021-11-01
EGAS00001005752 Multi-omic dataset of neuroendocrine neoplasm organoids Other
2021-11-03
EGAS00001005753 Genome-wide Rare Variant Score Associates With Morphological Subtypes of Autism Spectrum Disorder Other
2021-11-03
EGAS00001005755 Targeted sequencing data and shallow whole genome sequencing data of Follicular lymphoma. Other
2021-11-04
EGAS00001005756 WGS_11pcw_fetus_hdbr_15951_DNA Other
2021-11-04
EGAS00001005757 A critical spotlight on the paradigms of FFPE-DNA sequencing Other
2021-11-05
EGAS00001005758 Detection of Cancer Mutations by Urine Liquid Biopsy in Bladder Cancer Patients Other
2021-11-05
EGAS00001005759 DERMATLAS__Poroma_RNAseq Other
2021-11-05
EGAS00001005760 Genomics of pediatric myeloid neoplasms Other
2021-11-05
EGAS00001005761 Exome sequencing Other
2021-11-07
EGAS00001005764 JEM 20211004R Exome Sequencing
2021-11-08
EGAS00001005765 Whole-exome sequencing of paired tumour/blood of 58 T1 stage bladder cancer patients Other
2021-11-08
EGAS00001005766 Targeted sequencing of paired tumour/blood of 78 Ta stage bladder cancer patients Other
2021-11-08
EGAS00001005767 Targeted sequencing of paired tumour/blood of 34 T1 stage bladder cancer patients Other
2021-11-08
EGAS00001005769 Genetic and immune landscape evolution defines subtypes of MMR deficient colorectal cancer Other
2021-11-09
EGAS00001005770 Obesity and hyperinsulinemia drive adipocytes to activate a cell cycle program and senesce RNASeq
2021-11-10
EGAS00001005772 Acne GWAS meta-analysis Other
2021-11-10
EGAS00001005773 Multi-omic analysis of cell-of-origin and epigenomic state in pediatric H3K27M gliomas Other
2021-11-10
EGAS00001005781 Clinical impact of immune checkpoint inhibitor (ICI) response, DNA damage repair (DDR) gene mutations and immune-cell infiltration in subtypes of metastatic melanoma Other
2021-11-11
EGAS00001005782 Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkers Other
2021-11-11
EGAS00001005783 Deep whole genome ctDNA chronology of treatment-resistant prostate cancer Cancer Genomics
2021-11-11
EGAS00001005784 Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis Other
2021-11-12
EGAS00001005786 Extensive three-dimensional intratumor proteomic heterogeneity revealed by multiregion sampling in high-grade serous ovarian tumor specimens Other
2021-11-12
EGAS00001005787 Resolving the immune landscape of human prostate at a single cell level in health and cancer Other
2021-11-14
EGAS00001005788 Myeloma methylation Other
2021-11-14
EGAS00001005791 Mutations in ALK signaling pathways conferring resistance to ALK inhibitor treatment lead to collateral vulnerabilities in neuroblastoma cells Cancer Genomics
2021-11-15
EGAS00001005793 NOTCH-mutations drive immune-escape mechanisms in B cell malignancies Other
2021-11-16
EGAS00001005797 Mexican Biobank Project Population Genomics
2021-11-18
EGAS00001005798 Persistence of circulating tumor DNA in breast cancer patients during neoadjuvant treatment is a significant predictor of poor tumor response Other
2021-11-18
EGAS00001005807 RNA-seq data from 27 glioblastoma samples RNASeq
2021-11-19
EGAS00001005808 RNA sequencing data of in vitro differentiated megakaryocyte cells transduced with E527K and WT SRC Other
2021-11-19
EGAS00001005810 Amplified EPOR/JAK2 genes define a unique subtype of acute erythroid leukemia Other
2021-11-20
EGAS00001005812 Nanopore_and_Illumina_sequencing_of_human_glioblastomas Cancer Genomics
2021-11-22
EGAS00001005815 Sequencing data for CLL patients Other
2021-11-24
EGAS00001005816 B cell receptor repertoire kinetics after SARS-CoV-2 infection and vaccination Other
2021-11-24
EGAS00001005818 Longitudinal single-cell transcriptomics reveals distinct patterns of recurrence in acute myeloid leukemia RNASeq
2021-11-26
EGAS00001005819 Longitudinal single-cell transcriptomics reveals distinct patterns of recurrence in acute myeloid leukemia RNASeq
2021-11-26
EGAS00001005820 Longitudinal single-cell transcriptomics reveals distinct patterns of recurrence in acute myeloid leukemia Exome Sequencing
2021-11-26
EGAS00001005822 DNA sequencing for human normal endometrial glands Other
2021-11-29
EGAS00001005826 Failure of Differentiation of the Rhombic Lip Constitutes Medulloblastoma Other
2021-11-29
EGAS00001005827 The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin. Cancer Genomics
2021-11-29
EGAS00001005828 Molecular profiling of DLBCL patients treated in the PETAL trial Other
2021-11-29
EGAS00001005829 Whole exome sequencing of 12 NSCLC samples from 4 patients at MDACC Other
2021-11-29
EGAS00001005830 Full blood mRNA sequencing of myotonic dystrophy type 1 patients after cognitive behavioural therapy Other
2021-11-29
EGAS00001005832 DNA methylation analysis on PBL obtained from male patients with UC-PSC, UC and HC Other
2021-11-30
EGAS00001005833 Paired data of primary and relapse central nervous system lymphoma and testicular lymphoma Other
2021-11-30
EGAS00001005835 NLG-LBC-05 ctDNA Other
2021-11-30
EGAS00001005836 Gene expression-based prediction of pazopanib efficacy in sarcoma (HIPO, H021) Other
2021-11-30
EGAS00001005838 Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Landen, Stockholm, Sweden. Exome Sequencing
2021-12-01
EGAS00001005840 SPECTA RP-1759-AYA Sarcoma cohort Other
2021-12-02
EGAS00001005842 Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Umea, Sweden. Exome Sequencing
2021-12-02
EGAS00001005843 Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Edinburgh, Scotland, UK. Exome Sequencing
2021-12-02
EGAS00001005844 Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Dublin, Ireland. Exome Sequencing
2021-12-02
EGAS00001005845 Whole Exome Sequencing of Bipolar cases and controls performed at the Broad Institute on a cohort from Cardiff, UK (Craddock) Exome Sequencing
2021-12-02
EGAS00001005846 Orthotopic murine Group 3 medulloblastoma in C57Bl/6 mice treated with saline, cyclophosphamide or gemcitabine RNASeq
2021-12-03
EGAS00001005847 Orthotopic murine Group 3 medulloblastoma in C57Bl/6 mice treated with sham or craniospinal irradiation RNASeq
2021-12-03
EGAS00001005848 Searching for genetic modulators of the phenotypic heterogeneity in Brugada Syndrome Exome Sequencing
2021-12-03
EGAS00001005849 Optimisation of CITE-seq on liquid and solid tissues Other
2021-12-03
EGAS00001005850 TB-DAR Whole Genome Sequencing Study Other
2021-12-03
EGAS00001005854 Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Cambridge, UK Exome Sequencing
2021-12-03
EGAS00001005857 Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from the Netherlands (posthuma) Exome Sequencing
2021-12-03
EGAS00001005858 Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Germany Exome Sequencing
2021-12-03
EGAS00001005861 Single-nuclei gene-expression analysis of pheochromocytoma and paraganglioma links tumor subtypes with tumor microenvironment Other
2021-12-06
EGAS00001005863 Identification of the dismal subtype of B-ALL with dysregulation of CDX2 and UBTF Other
2021-12-07
EGAS00001005864 Nascent transcriptome in T-ALL bone marrow Other
2021-12-07
EGAS00001005865 Paired healthy & tumor organoid Biobank _B15PON Cancer Genomics
2021-12-08
EGAS00001005866 RNA-seq following miR-130a knock-down (KD) in Flag-tag AML1-ETO Kasumi-1 cells Other
2021-12-08
EGAS00001005867 CUT&RUN of AML1-ETO binding occupancy following miR-130a KD in Kasumi-1 cells Other
2021-12-08
EGAS00001005868 RNA-seq following miR-130a overexpression (OE) in human CD34+cord blood cells Other
2021-12-08
EGAS00001005869 RNA-seq following TBL1XR1 KD in human CD34+CD38- cord blood cells Other
2021-12-08
EGAS00001005870 tFL with a PMBL GE signature Other
2021-12-08
EGAS00001005872 Defining structural variation associated with breast cancer susceptibility by long-read genome sequencing Other
2021-12-08
EGAS00001005873 Effects of nucleases on cell-free extrachromosomal circular DNA Other
2021-12-09
EGAS00001005874 Identification of Germline Monoallelic Mutations in IKZF2 in Patients with Immune Dysregulation. Other
2021-12-09
EGAS00001005875 Molecular and clinical effects of selective TYK2 inhibition with deucravacitinib in psoriasis Other
2021-12-13
EGAS00001005876 Comprehensive characterization of pre- and post-treatment samples of breast cancer reveal potential mechanisms of chemotherapy resistance Other
2021-12-13
EGAS00001005878 A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia Other
2021-12-13
EGAS00001005879 Deciphering RBP - alternative splicing networks in ALS iPSC-MN: patient and control datasets Other
2021-12-13
EGAS00001005880 Deciphering RBP - alternative splicing networks in ALS iPSC-MN: TDP-43, NOVA1, NOVA2 and RBFOX2 eCLIP-seq Other
2021-12-13
EGAS00001005881 Deciphering RBP - alternative splicing networks in ALS iPSC-MN: NOVA1 gain and loss of function systems Other
2021-12-13
EGAS00001005887 Patient-derived tumor organoids for personalized medicine in a rare case of hepatocellular carcinoma with neuroendocrine differentiation. Other
2021-12-14
EGAS00001005891 Comparison of fresh and slow-frozen cancer samples for different applications Other
2021-12-16
EGAS00001005892 Functional Mapping of AKT Signaling and Biomarkers of Response From the FAIRLANE Trial of Neoadjuvant Ipatasertib Plus Paclitaxel for Triple-Negative Breast Cancer Other
2021-12-17
EGAS00001005893 Initial cohort of 500 solid tumors screened for Basket of Baskets Cancer Genomics
2021-12-17
EGAS00001005895 INSIGHT: VHL Case Report Other
2021-12-17
EGAS00001005897 Origins and timing of emerging lesions in advanced renal cell carcinoma Other
2021-12-19
EGAS00001005899 Targeted de novo phasing and long-range assembly by template mutagenesis Population Genomics
2021-12-20
EGAS00001005900 Gut metagenome associations with extensive digital health data in a volunteer-based EstMB cohort Other
2021-12-21
EGAS00001005902 Whole genome and exome sequencing data of invasive micropapillary carcinoma of breast Other
2021-12-22
EGAS00001005904 A transcriptome atlas of human skeletal muscles Other
2021-12-23
EGAS00001005905 Reproducibility of 10x Genomics single cell RNA sequencing method in the immune cell environment Other
2021-12-27
EGAS00001005906 Exome-wide mutation analysis of cell-free DNA to simultaneously monitor the full spectrum of cancer treatment outcomes Other
2021-12-30
EGAS00001005908 Transcriptome analysis of endometrial organoids derived from patients with Mayer-Rokitansky-Küster-Hauser syndrome Other
2021-12-30
EGAS00001005909 Rare occurrence of Aristolochic Acid Mutational Signatures in Oro-Gastrointestinal Tract Cancers Other
2022-01-04
EGAS00001005910 Genome-wide genotype data for 1,433 ni-Vanuatu Other
2022-01-04
EGAS00001005911 Epigenomic priming of immune genes implicates oligodendroglia in multiple sclerosissusceptibility Other
2022-01-05
EGAS00001005912 Sequencing of an organoid biobank for childhood soft tissue sarcoma. Other
2022-01-05
EGAS00001005914 Target gene sequencing for human normal endometrial glands Other
2022-01-06
EGAS00001005926 Genomic determination for Homologous Recombination Deficiency (HRD) by shallow Whole Genome Sequencing (sWGS) Other
2022-01-06
EGAS00001005931 COVID-19 Severity of First Wave of Infection for Severe Patients in Madrid Other
2022-01-07
EGAS00001005932 Methylation profiling of osteoblastomas and their mimics Other
2022-01-07
EGAS00001005933 Myoepithelial progenitors as founder cells of hyperplastic human breast lesions upon PIK3CA transformation Other
2022-01-09
EGAS00001005935 The European MAPPYACTS trial: Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies Other
2022-01-10
EGAS00001005937 Paired healthy & tumor organoid Biobank _B16PON Other
2022-01-11
EGAS00001005939 Human induced pluripotent stem cells display a similar mutation burden as embryonic pluripotent cells in vivo Other
2022-01-12
EGAS00001005940 Molecular analysis in bowel malignancies in cancer survivors vs. primary malignancies Cancer Genomics
2022-01-13
EGAS00001005941 T-cell reconstitution after reduced dose ATLG induction in kidney transplant recipients Other
2022-01-14
EGAS00001005945 Combination therapies to inhibit LCK tyrosine kinase and mTOR signaling in T-cell Acute Lymphoblastic Leukemia Other
2022-01-18
EGAS00001005947 Patient-derived organoids_Vumc Cancer Genomics
2022-01-18
EGAS00001005948 RNA-seq on patient-derived, stage II, CRC cell lines Other
2022-01-18
EGAS00001005949 Overexpression of the miR-17-92 cluster in colorectal adenoma organoids induces a carcinoma-like genotype Cancer Genomics
2022-01-18
EGAS00001005950 The Proteogenomic Subtypes of Acute Myeloid Leukemia Other
2022-01-18
EGAS00001005951 RNA sequencing of 12 NSCLC samples from 4 patients at MDACC Other
2022-01-18
EGAS00001005952 Tumor-intrinsic expression of the autophagy gene Atg16l1 suppresses anti-tumor immunity in colorectal cancer Other
2022-01-20
EGAS00001005953 Targeted sequencing of diffuse large B-cell lymphoma tumour samples from the UK's Haematological Malignancy Research Network Other
2022-01-20
EGAS00001005954 RNA-sequencing data from metastatic Castration-Resistant Prostate Cancer (mCRPC) Other
2022-01-20
EGAS00001005955 Monocyte and macrophage lipid accumulation results in downregulated type-I interferon responses Other
2022-01-20
EGAS00001005957 Oesophageal adenocarcinoma whole exome and RNA-seq raw sequencing data Cancer Genomics
2022-01-21
EGAS00001005963 Ductal keratin 15+ luminal progenitors in normal breast exhibit a basal-like breast cancer transcriptomic signature Other
2022-01-25
EGAS00001005965 TLR7 variants in human lupus patients Exome Sequencing
2022-01-26
EGAS00001005969 LifeLines-NEXT pilot study Other
2022-01-28
EGAS00001005970 Genome analysis of early onset sporadic rectal cancer Cancer Genomics
2022-01-28
EGAS00001005971 Evaluating the immune response in treatment-naive hospitalised patients with influenza and COVID-19 Other
2022-01-28
EGAS00001005972 H3Africa - Consortium WGS Other
2022-01-28
EGAS00001005973 ENCORAFENIB COMBINED WITH BINIMETINIB FOR BRAFV600E-MUTATED RELAPSED/REFRACTORY MULTIPLE MYELOMA: THE PHASE II GMMG-BIRMA TRIAL (Hipo_K08K) Other
2022-01-28
EGAS00001005974 An Isogenic Cell Line Panel for Sequence-based Screening of Targeted Anti-cancer Drugs Other
2022-01-28
EGAS00001005975 850k Methyome analysis of snap frozen or FFPE stored human MBM Other
2022-01-29
EGAS00001005976 Molecular programs of melanoma brain metastases (MBM) Other
2022-01-29
EGAS00001005978 Bulk RNA sequencing of Singapore colorectal cancer patients (SG-BULK) Other
2022-01-31
EGAS00001005980 Unravelling the contribution of HIF pathway and its therapeutic potential in human AML leukemia-initiating cells Other
2022-01-31
EGAS00001005981 Longitudinal profiling of circulating tumour DNA for tracking tumour dynamics in pancreatic cancer Other
2022-01-31
EGAS00001005982 Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis Other
2022-01-31
EGAS00001005983 Epithelioid sarcoma sequencing data Other
2022-01-31
EGAS00001005984 The genomic and immune landscape of long-term survivors of high-grade serous ovarian cancer Other
2022-02-01
EGAS00001005985 The polarity and specificity of antiviral T lymphocyte responses determine susceptibility to SARS-CoV-2 infection in cancer patients and healthy individuals. Other
2022-02-01
EGAS00001005986 Biallelic HMBS Inactivation Defines a Homogenous Clinico-Molecular Subtype of Hepatocellular Carcinoma Other
2022-02-01
EGAS00001005992 Cell-free DNA and bone marrow samples from myelodysplastic syndromes Other
2022-02-03
EGAS00001005993 Host genotyping data from Dutch adult bacterial meningitis patients and linked bacterial genome sequences Other
2022-02-03
EGAS00001005995 To determine the genomic profile of Triple Negative Breast Cancer patient-derived xenografts (PDX cohort) Other
2022-02-03
EGAS00001005997 Bioinformatics analysis of chimerism in monochorionic dizygotic twins Other
2022-02-04
EGAS00001006001 Combination of ribociclib and gemcitabine for the treatment of medulloblastoma Other
2022-02-04
EGAS00001006002 Specific BRCA and immune configurations determine optimal response to platinum-based chemotherapy in triple negative breast and ovarian carcinomas (COH_TNBC_RNAseq) Other
2022-02-04
EGAS00001006004 Multimodal immunogenomic biomarker analysis of tumors from pediatric patients enrolled to a phase 1-2 study of single-agent atezolizumab Other
2022-02-05
EGAS00001006005 A Proteogenomic Analysis of Clear Cell Renal Cell Carcinoma in a Chinese Population Other
2022-02-05
EGAS00001006006 Whole Exome sequencing of colorectal cancer patients (SG-BULK) Other
2022-02-07
EGAS00001006007 Genomic and transcriptome analysis for intrahepatic cholangiocarcinoma Cancer Genomics
2022-02-07
EGAS00001006008 PROJET DREPANOCYTOSE ET PALUDISME Other
2022-02-07
EGAS00001006009 CCL22 chemokine mutations drive natural killer cell lymphoproliferative disease by biasing GPCR signaling Other
2022-02-07
EGAS00001006010 Human genome-wide variations in the Massim region Other
2022-02-07
EGAS00001006011 Genomic diversity of Vietnamese Other
2022-02-07
EGAS00001006012 To determine the transcriptional profiles of Ovarian carcinomas (UW cohort) Other
2022-02-07
EGAS00001006013 Single cell RNA sequencing of colorectal cancer patients (CRC-SG1) Other
2022-02-08
EGAS00001006015 DNA methylation profiles of samples included in the EORTC 26091 TAVAREC trial Epigenetics
2022-02-08
EGAS00001006016 Drug-induced epigenomic plasticity reprograms circadian rhythm regulation to drive prostate cancer towards androgen-independence (RNA-seq) Other
2022-02-09
EGAS00001006017 Drug-induced epigenomic plasticity reprograms circadian rhythm regulation to drive prostate cancer towards androgen-independence (ChIP-seq) Other
2022-02-09
EGAS00001006019 Disease specific alterations in the olfactory mucosa of patients with Alzheimer’s disease Other
2022-02-09
EGAS00001006020 Methylome sequencing of cell-free DNA and RRBS of solid tissue Other
2022-02-09
EGAS00001006021 The neo-open reading frame peptides that comprise the tumor framome are a rich source of neoantigens for cancer immunotherapy Cancer Genomics
2022-02-10
EGAS00001006022 Whole-exome sequencing of glioblastomas with long-term relapse interval Other
2022-02-10
EGAS00001006024 Application of high-throughput, high-depth, targeted single-nucleus DNA sequencing in pancreatic cancer Other
2022-02-10
EGAS00001006025 Papuan Y chromosome Diversity Panel Other
2022-02-11
EGAS00001006027 Targeted analysis of cell-free circulating tumor DNA is suitable for early relapse and actionable target detection in patients with neuroblastoma Cancer Genomics
2022-02-11
EGAS00001006028 IYDP Indonesian Y chromosome Diversity Project Other
2022-02-11
EGAS00001006030 Whole genome sequencing of colorectal cancer patients (SG-BULK-1) Other
2022-02-13
EGAS00001006031 Genomewide copy number alteration screening of circulating plasma DNA Other
2022-02-13
EGAS00001006033 Genome-wide DNA Methylation Data from Illumina HumanMethylationEPIC arrays for whole blood samples from 403 healthy individuals Other
2022-02-14
EGAS00001006034 The clinical utility of genomics in childhood cancer extends beyond targetable mutations Other
2022-02-15
EGAS00001006035 WGS of iPSC from TOF patients with/without DG and healthy control Whole Genome Sequencing
2022-02-15
EGAS00001006036 PAX4 loss of function increases diabetes risk by altering human pancreatic endocrine cell development RNASeq
2022-02-15
EGAS00001006037 The KATHERINE study of adjuvant trastuzumab emtansine in HER2-positive breast cancer: analysis of patients with HER2-negative residual invasive disease on re-testing Other
2022-02-16
EGAS00001006038 GINS3 fibroblast RNAseq Other
2022-02-16
EGAS00001006039 Whole Genome sequencing of colorectal cancer patients (SG-BULK-2) Other
2022-02-17
EGAS00001006040 Comparison of sequencing assays for sensitive detection of circulating tumour DNA in stage IA-IV breast cancer Other
2022-02-17
EGAS00001006042 Anti-Cancer Therapies Induce Mutations in Adult Stem Cells in a Tissue-Specific Manner Forensic or Paleo-genomics
2022-02-18
EGAS00001006043 Whole Exome Sequencing PPGL Other
2022-02-18
EGAS00001006044 Transcriptome Sequencing PPGL Other
2022-02-18
EGAS00001006045 Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___visium Other
2022-02-18
EGAS00001006048 To determine the genomic profiles of Ovarian carcinomas (UW cohort) Other
2022-02-18
EGAS00001006049 Single cell RNA sequencing of colorectal cancer patients (KUL3/KUL5) Other
2022-02-21
EGAS00001006050 CIRdb: Array genotype data Other
2022-02-21
EGAS00001006051 WGS of gastric cancer in the Japanese population (81 gastric cancers of NCC) Other
2022-02-22
EGAS00001006052 Microenvironment subtypes and association with tumor cell mutations and antigen expression in follicular lymphoma Other
2022-02-22
EGAS00001006053 Insights from genome-wide data from Thailand and Laos Other
2022-02-22
EGAS00001006055 Oncogenic cooperation in a human de novo T-ALL model Other
2022-02-22
EGAS00001006056 Whole Genome sequencing of colorectal cancer patients (SG-BULK-3) Other
2022-02-23
EGAS00001006058 Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants Other
2022-02-24
EGAS00001006059 Chromatin profiles classify castration-resistant prostate cancers suggesting therapeutic targets Other
2022-02-24
EGAS00001006060 Genetics of non-syndromic idiopathic autism spectrum disorders in India Other
2022-02-25
EGAS00001006062 A multi-center genome-wide association study for nasopharyngeal carcinoma Population Genomics
2022-02-28
EGAS00001006063 Enhanced cortical neural stem cell identity through SMAD/WNT inhibition in human cerebral organoids facilitates emergence of outer radial glial cells Other
2022-02-28
EGAS00001006068 Integrative analysis of non-small cell lung cancer patient-derived xenografts identifies unique proteotypes associated with patient outcomes Other
2022-02-28
EGAS00001006069 Genomic landscape of malignant peripheral nerve sheath tumor (MPNST) Other
2022-02-28
EGAS00001006072 Clear cell sarcoma sequencing data Other
2022-03-01
EGAS00001006073 Genomic and transcriptomic analysis of baseline PDAC patients' tumors from the OXIRI phase 1b clinical trial Other
2022-03-02
EGAS00001006085 To determine the genomic profiles of Triple Negative Breast Cancers (COH cohort) Other
2022-03-03
EGAS00001006088 The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin. Cancer Genomics
2022-03-03
EGAS00001006089 Genomic History of Siberia Population Genomics
2022-03-03
EGAS00001006090 The Spatial Heterogeneity in Multiple Myeloma - from the Subclonal Architecture to the Immune Microenvironment (partly hipo_K08K) Other
2022-03-03
EGAS00001006091 Res1_H23_exp1_MC_04_03_22 Cancer Genomics
2022-03-04
EGAS00001006092 Res1_HT29_exp1_MC_02_03_22 Cancer Genomics
2022-03-04
EGAS00001006093 Res1_HT29_exp2_MC_03_03_22 Cancer Genomics
2022-03-04
EGAS00001006096 Tumour evolvability metrics predict recurrence in advanced localised prostate cancer (tumour data) Cancer Genomics
2022-03-04
EGAS00001006098 Tumour evolvability metrics predict recurrence in advanced localised prostate cancer (normal data) Cancer Genomics
2022-03-04
EGAS00001006101 Whole Genome sequencing of colorectal cancer patients (SG-BULK-4) Other
2022-03-05
EGAS00001006102 A genome-wide association study for nasopharyngeal carcinoma in Hong Kong population Population Genomics
2022-03-06
EGAS00001006103 High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform Other
2022-03-07
EGAS00001006105 Profiling of 27 type 2 diabetes GWAS loci using next-generation (NG) capture C in a human beta-cell model Other
2022-03-08
EGAS00001006106 Single cell analyses of transcriptome and epigenome in neuroblastoma infiltrated bone marrow Other
2022-03-08
EGAS00001006107 Adult B-precursor acute lymphoblastic leukemia transcriptomes Other
2022-03-09
EGAS00001006112 RNAseq Iron-Treated iPSC-derived Microglia Other
2022-03-10
EGAS00001006113 Spatio-temporal analysis of prostate tumors in situ suggests pre-existence of treatment-resistant clones Other
2022-03-10
EGAS00001006114 Whole Genome sequencing of colorectal cancer patients (SG-BULK-5) Other
2022-03-11
EGAS00001006115 Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature Other
2022-03-11
EGAS00001006116 Genomic History of the Solomon Islands Other
2022-03-11
EGAS00001006117 CDK4 phosphorylation predicts high sensitivity of malignant pleural mesotheliomas to CDK4/6 inhibition Other
2022-03-11
EGAS00001006118 Conserved features of TERT promoter duplications reveal an activation mechanism that mimics hotspot mutations in cancer Other
2022-03-12
EGAS00001006119 Total RNA sequencing of RNA from testicular tissue RNASeq
2022-03-12
EGAS00001006120 Stromal-induced epithelial-mesenchymal transition induces drug resistance in acute lymphoblastic leukemia Other
2022-03-14
EGAS00001006122 The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin. Cancer Genomics
2022-03-14
EGAS00001006123 Genetic immune escape landscape in primary and metastatic cancer Other
2022-03-15
EGAS00001006124 Spatial atlas of clonal copy number alterations in co-existing benign and malignant tissue Other
2022-03-15
EGAS00001006125 Engineered Human Primary T Cell transcriptome study Other
2022-03-15
EGAS00001006126 early-stage ESCC sequencing study Other
2022-03-16
EGAS00001006127 RNASeq of Calcoco2 in beta and fat cell lines Other
2022-03-16
EGAS00001006132 Denisova admixture in Southeast Asia and Oceania Other
2022-03-17
EGAS00001006133 Discriminating Th17.1 cell driven sarcoidosis-like inflammation from relapse after anti-BCMA CAR T cells in multiple myeloma Other
2022-03-18
EGAS00001006134 Longitudinal monitoring of disease burden and response using ctDNA from dried blood spots in xenograft models Whole Genome Sequencing
2022-03-18
EGAS00001006135 Stage-specific gene and transcript dynamics in human male germ cells Other
2022-03-18
EGAS00001006136 single cell RNA-seq and ATAC-seq of human fetal forebrain tissue Other
2022-03-19
EGAS00001006137 Smoking-dependent expression alterations in nasal epithelium reveal immune impairment linked to germline variation and lung cancer risk Transcriptome Analysis
2022-03-19
EGAS00001006138 Drug screen in iPSC-Neurons identifies nucleoside analogs as inhibitors of (G4C2)n expression in C9orf72 ALS/FTD Other
2022-03-21
EGAS00001006139 The molecular response of skeletal muscle,adipose tissue and blood in life-long high-level trained and untrained men and women after acute exercise Transcriptome Sequencing
2022-03-21
EGAS00001006140 Loss of Epigenetic Barrier is Required for Enhancer Hijacking-Mediated Oncogenic Transcription Other
2022-03-21
EGAS00001006141 Integrated single-cell profiling dissects cell-state-specific enhancer landscapes of human tumor infiltrating T cells. Epigenetics
2022-03-21
EGAS00001006142 Genome-wide cell-free DNA termini in patients with cancer Other
2022-03-22
EGAS00001006143 FACS sorting of ploidy populations in an undifferentiated soft tissue sarcoma for RRBS Other
2022-03-22
EGAS00001006144 USARC 10X Genomics Single Cell DNA Sequencing Data Other
2022-03-22
EGAS00001006147 Whole exome sequencing study of cholesteatoma patients from affected families Other
2022-03-23
EGAS00001006148 Genomic profiling of metastatic basal cell carcinoma reveals candidate drivers of disease and therapeutic targets Cancer Genomics
2022-03-24
EGAS00001006154 Detection of uniparental disomy from genome sequencing of family trio Other
2022-03-24
EGAS00001006155 Detection of maternal DNA contamination in the placenta Other
2022-03-24
EGAS00001006157 miRNA regulation of monocyte expressed inflammatory genes in patients with inflammatory bowel disease Transcriptome Analysis
2022-03-25
EGAS00001006158 Exome sequencing in CLL re-treated with venetoclax Exome Sequencing
2022-03-26
EGAS00001006159 Epigenomic data of Human muscle stem cell Other
2022-03-28
EGAS00001006161 Enhancer profiling to identify identifies epigenetic markers of endocrine resistance in metastatic castration resistant prostate cancer patients Epigenetics
2022-03-28
EGAS00001006164 Validation of a targeted sequencing panel for multiple myeloma Cancer Genomics
2022-03-29
EGAS00001006166 Molecular landscape of blastic plasmacytoid dendritic cell neoplasm Other
2022-03-30
EGAS00001006167 LCM-ATACseq on human lung macrophages Other
2022-03-30
EGAS00001006168 LCM-RNAseq on human lung macrophages Other
2022-03-30
EGAS00001006169 Res1_PC9_exp1_MC_29_03_22 Cancer Genomics
2022-03-30
EGAS00001006170 Res1_PC9_exp2_MC_01_04_22 Cancer Genomics
2022-03-30
EGAS00001006172 A Dose Escalation Study of Efmarodocokin Alfa (UTTR1147A) in Healthy Volunteers and Patients with Ulcerative Colitis Other
2022-03-31
EGAS00001006173 Phase 1 CX-5461 Trial (Canadian Cancer Trials Group Trial IND.231) Other
2022-03-31
EGAS00001006174 Small molecule inhibitors of LOXL synergize with 5-AZA to restore erythropoiesis in myeloid neoplasms Other
2022-03-31
EGAS00001006175 Characterization of Cell Free Plasma Methyl-DNA From Xenografted Tumors to Guide the Selection of Diagnostic Markers for Early-Stage Cancers Other
2022-04-01
EGAS00001006176 Genomic insights into the population history of the Resande or Swedish Travellers Other
2022-04-01
EGAS00001006184 Mapping genetic effects on cell type-specific chromatin accessibility using single nucleus ATAC-seq Other
2022-04-05
EGAS00001006185 Variants from a subset of genes from WES of adult AML patient samples Other
2022-04-05
EGAS00001006186 Dual spatially resolved transcriptomics for human host-pathogen colocalization studies in FFPE tissue sections Other
2022-04-05
EGAS00001006187 Case Report: Precision medicine target revealed by in-vitro modelling of relapsed, refractory ALL from a child with neurofibromatosis Other
2022-04-05
EGAS00001006191 Molecular and clinical diversity in primary central nervous system lymphoma: a LOC Network study Other
2022-04-06
EGAS00001006195 RNA sequencing of AD, MCI and control OM cells Other
2022-04-07
EGAS00001006196 Androgen receptor blockade promotes response to BRAF/MEK-targeted therapy Other
2022-04-07
EGAS00001006198 Heat selection enables highly scalable methylome profiling in cell-free DNA for noninvasive monitoring of cancer patients Other
2022-04-11
EGAS00001006200 Clonal somatic copy number altered driver events inform drug sensitivity in high-grade serous ovarian cancer Other
2022-04-11
EGAS00001006201 Serum proteomics of aortic diseases Other
2022-04-11
EGAS00001006202 Separation, characterization, and identification of individuals from multi-person blood mixtures with single cell transcriptome sequencing and a novel bioinformatics pipeline Other
2022-04-11
EGAS00001006203 A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome Other
2022-04-12
EGAS00001006204 Molecular Classification of Hormone Sensitive and Castration Resistant prostate cancer, using non-negative matrix factorization molecular subtyping Other
2022-04-13
EGAS00001006205 Genetic and methylation profiles distinguish benign, malignant and spitzoid melanocytic tumors Other
2022-04-13
EGAS00001006206 ATAC Sequencing of 4 CLL patient samples Other
2022-04-14
EGAS00001006211 Gremlin 1 + fibroblastic niche maintains dendritic cell homeostasis in lymphoid tissues Other
2022-04-16
EGAS00001006212 WXS and RNA-seq for 22 patients treated with radiation + immunotherapy Other
2022-04-17
EGAS00001006213 Somatic L1 retrotranspositions in normal human cells Other
2022-04-18
EGAS00001006214 scRNA mCRC PDO Other
2022-04-19
EGAS00001006215 Transcriptomic analysis of peripheral blood dendritic cells and monocytes from patients with familial chilblain lupus and hetereozygous mutations in TREX1 Transcriptome Analysis
2022-04-19
EGAS00001006218 Clonal hematopoiesis is associated with adverse outcomes in patients with COVID-19 Other
2022-04-25
EGAS00001006222 MGP Panel: a comprehensive targeted genomics panel for molecular profiling of multiple myeloma patients Other
2022-04-25
EGAS00001006228 Serum Proteome Profiling Identifies Early Markers of Therapeutic Response to Neoadjuvant Chemotherapy of Breast Cancer Other
2022-04-25
EGAS00001006229 Biomarker Data from KATHERINE: A Phase III Study of Adjuvant Trastuzumab Emtansine versus Trastuzumab in Patients with Residual Invasive Disease after Neoadjuvant Therapy for HER2-Positive Breast Cancer Other
2022-04-26
EGAS00001006230 Extensive patient-to-patient single nuclei transcriptome heterogeneity in pheochromocytomas and paragangliomas Other
2022-04-26
EGAS00001006232 Salivary Gland Cancer TSO500 dataset Other
2022-04-27
EGAS00001006233 Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis Other
2022-04-28
EGAS00001006234 Hereditary_Cerebellar_Ataxias___Whole_Genome_Sequencing___2021 Whole Genome Sequencing
2022-04-28
EGAS00001006235 Whole exome sequencing of PMBCL Other
2022-04-29
EGAS00001006236 glioblastoma single cell RNAseq Other
2022-04-29
EGAS00001006237 A brain precursor atlas reveals the acquisition of developmental-like states in adult cerebral tumours Other
2022-04-29
EGAS00001006240 PIAMA nasal RNAseq data Other
2022-05-01
EGAS00001006242 RNA-sequencing of mechanical stress induced osteoarthritis-like damage in aged human cartilage explants treated with the anti-deiodinase iopanoic acid Other
2022-05-02
EGAS00001006246 Single-cell RNA-seq data from 3 HGSOC patient-derived organoids and corresponding tumor or ascites Other
2022-05-02
EGAS00001006247 Genomics characterization of BRAF-V600E colorectal cancer patients treated with anti-BRAF/EGFR Exome Sequencing
2022-05-02
EGAS00001006249 Molecular characterization of a renal cell carcinoma PDX cohort Cancer Genomics
2022-05-05
EGAS00001006251 Accumulation of copy number alterations and clinical progression across advanced prostate cancer Other
2022-05-05
EGAS00001006252 The University of Hong Kong Gastric Cancer Organoids RHO Signaling Study Other
2022-05-06
EGAS00001006254 Germline sequencing Other
2022-05-07
EGAS00001006257 The Gut Microbiome of renal transplant recipients – Cross-sectional Other
2022-05-09
EGAS00001006258 The Gut Microbiome of liver transplant recipients – Cross-sectional + Longitudinal (renal and liver) Other
2022-05-09
EGAS00001006260 Discovery of a highly widespread bacteriophage family and its associations to metabolic syndrome gut microbiomes Other
2022-05-09
EGAS00001006262 Induced pluripotent stem cell lines (iPSC lines) produced from skin and blood cells. Other
2022-05-11
EGAS00001006263 Single-cell analysis reveals transcriptomic and epigenomic impacts on the maternal-fetal interface upon SARS-CoV-2 infection Other
2022-05-12
EGAS00001006265 Bulk and single-cell AML RNA-seq post ex vivo culture Other
2022-05-12
EGAS00001006266 Genetic Determinants of Mannose-binding Lectin Activity Predispose to Thromboembolic Complications in Critical COVID-19 Other
2022-05-12
EGAS00001006267 Transcriptome analysis of samples derived from GBM tumors, and relevant cell lines established and maintained at 5% or 20% oxygen. Other
2022-05-12
EGAS00001006268 ATM germline variants in a young adult with chronic lymphocytic leukemia: 8 years of genomic evolution Cancer Genomics
2022-05-13
EGAS00001006273 RFX6-mediated dysregulation defines human β cell dysfunction in early type 2 diabetes Transcriptome Analysis
2022-05-14
EGAS00001006274 Whole Exome Sequencing of Schizophrenia cases and controls performed at the Broad Institute on a cohort from Bristol, UK Exome Sequencing
2022-05-16
EGAS00001006275 Characterization of alternative promoter usage in advanced prostate cancer RNASeq
2022-05-16
EGAS00001006276 Germline variant analysis in childhood AML Other
2022-05-17
EGAS00001006280 A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome Other
2022-05-17
EGAS00001006281 COPD and neutrophils Other
2022-05-17
EGAS00001006282 Evolutionary histories of breast cancer and related clones Cancer Genomics
2022-05-18
EGAS00001006283 Altered neutrophil and granulopoiesis biology underlie a poor outcome sepsis endotype Transcriptome Analysis
2022-05-18
EGAS00001006284 COVID-19 GWAS in Japanese Other
2022-05-19
EGAS00001006285 Deep whole genome sequencing identifies recurrent genomic alterations in breast cancer cell lines and patient derived xenograft models Other
2022-05-20
EGAS00001006286 Combination of CDK4/6 with BET-bromodomain and PI3K/mTOR inhibitors in medulloblastoma in vitro and in vivo Other
2022-05-20
EGAS00001006288 Combined – whole blood and skin fibroblasts - transcriptomic analysis in Psoriatic arthritis. Other
2022-05-21
EGAS00001006289 An alternative splicing modulator decreases mutant HTT and improves the molecular fingerprint in Huntington’s disease patient neurons Other
2022-05-22
EGAS00001006293 Oncogenic chimeric transcription factors drive tumor-specific transcription, processing, and translation of silent genomic regions Other
2022-05-23
EGAS00001006294 Whole genome sequencing of multifocal small intestinal neuroendocrine tumors Whole Genome Sequencing
2022-05-23
EGAS00001006295 Whole exome and genome sequencing investigations of perinatal death Other
2022-05-24
EGAS00001006298 The immunopeptidome landscape associated with T cell infiltration, inflammation and immune-editing in lung cancer Other
2022-05-24
EGAS00001006299 RP-1843 Arcagen - Gastrointestinal rare cancers (GI) Other
2022-05-24
EGAS00001006300 Human Developmental Biology Resource (HDBR) abnormal fetal samples Exome Sequencing
2022-05-24
EGAS00001006305 Low input capture Hi-C (liCHi-C) identifies promoter-enhancer interactions at high-resolution. Other
2022-05-24
EGAS00001006306 Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis Other
2022-05-25
EGAS00001006308 A Risk Score Incorporating Low Pass Whole Genome Sequencing of Cell Free DNA from Patients Receiving CD19 CAR T-Cell Therapy for Large B-Cell Lymphoma Whole Genome Sequencing
2022-05-26
EGAS00001006309 HNF1A haploinsufficiency causes decreased insulin expression, dysregulation of pancreatic progenitor signature genes and affects chromatin accessibility RNASeq
2022-05-26
EGAS00001006313 Single cell transcriptomics of hESC-derived midbrain dopaminergic neurons generated by a new human development-based protocol Other
2022-05-27
EGAS00001006314 Loss of RREB1 in pancreatic beta cells reduces cellular insulin content and affects endocrine cell gene expression Other
2022-05-27
EGAS00001006317 Shallow nanopore RNA sequencing enables transcriptome profiling for precision cancer medicine (Hipo_021) Cancer Genomics
2022-05-30
EGAS00001006320 Childhood Cancer Model Atlas Other
2022-06-01
EGAS00001006321 Fragment ends of circulating microbial DNA as signatures for infectious diseases Other
2022-06-02
EGAS00001006322 COPD and neutrophils sc Other
2022-06-03
EGAS00001006323 COPD and neutrophils sc rhapsody Other
2022-06-05
EGAS00001006327 Detection of early seeding of Richter transformation in chronic lymphocytic leukemia Other
2022-06-06
EGAS00001006328 Long-read sequencing for cell-free DNA analysis (human) Other
2022-06-07
EGAS00001006329 Long-read sequencing for cell-free DNA analysis (mouse) Other
2022-06-07
EGAS00001006330 Spatial multi-omic map of human myocardial infarction Other
2022-06-07
EGAS00001006331 Intratumoural heterogeneity and immune modulation in lung adenocarcinoma of female smokers and never smokers Other
2022-06-07
EGAS00001006332 A clinically annotated post-mortem approach to study multi-organ somatic mutational clonality in normal tissues Exome Sequencing
2022-06-07
EGAS00001006334 Targeting the bicarbonate transporter SLC4A4 overcomes immunosuppression and immunotherapy resistance in pancreatic cancer Other
2022-06-08
EGAS00001006336 Genomics of drug sensitivity in acute lymphoblastic leukemia Other
2022-06-09
EGAS00001006339 Platelet RNAseq data for SLFN14 K219N patients Other
2022-06-10
EGAS00001006340 Genetic and epigenetic variation at regulatory regions contribute to cancer evolution under endocrine treatment Other
2022-06-10
EGAS00001006342 Molecular determinants of outcomes in relapsed mantle cell lymphoma treated with ibrutinib or temsirolimus in the MCL3001 (RAY) trial Cancer Genomics
2022-06-10
EGAS00001006343 Single cell genomic variation induced by mutational processes in cancer Other
2022-06-10
EGAS00001006344 Placebo-only arm transcriptomic analysis of the phase 3 PROTECT clinical trial Other
2022-06-13
EGAS00001006345 Genetic regulation of gene expression in human brain cell types Other
2022-06-14
EGAS00001006347 Single cell whole genome sequencing of high hyperdiploid acute lymphoblastic leukemia Other
2022-06-14
EGAS00001006348 The admixture histories of Cabo Verde Population Genomics
2022-06-14
EGAS00001006350 molecular profiles of serum-derived extracellular vesicles in high-grade serous ovarian cancer Other
2022-06-14
EGAS00001006351 Rhabdoid tumor sequencing data Other
2022-06-15
EGAS00001006352 Brain tumor sequencing data Other
2022-06-15
EGAS00001006353 Diffuse Intrinsic Pontine Glioma Other
2022-06-15
EGAS00001006354 Acute myeloid leukemia sequencing data Other
2022-06-15
EGAS00001006355 Glioma sequencing data Other
2022-06-15
EGAS00001006356 Soft tissue sarcoma sequencing data Cancer Genomics
2022-06-15
EGAS00001006357 early-Duodenal Cancer sequencing study Other
2022-06-15
EGAS00001006358 Clonal dominance defines metastatic dissemination in pancreatic cancer Other
2022-06-15
EGAS00001006362 Juntendo Muscle Study (JMS) Other
2022-06-17
EGAS00001006363 Muscle SATellite cell study (MSAT) Other
2022-06-17
EGAS00001006364 Single-cell multi-omics of human clonal hematopoiesis reveals that DNMT3A R882 mutations perturb early progenitor states through selective hypomethylation. Cancer Genomics
2022-06-17
EGAS00001006365 Widespread hypertranscription in aggressive human cancers Other
2022-06-17
EGAS00001006369 RNA-seq analysis of metastatic prostate cancer solid tumor biopsies Other
2022-06-20
EGAS00001006370 Transcriptome sequencing in monozygotic twins discordant for Mayer-Rokitansky-Küster-Hauser syndrome Transcriptome Analysis
2022-06-20
EGAS00001006371 Genome sequencing in monozygotic twins discordant for Mayer-Rokitansky-Küster-Hauser syndrome Whole Genome Sequencing
2022-06-20
EGAS00001006372 Presence of rare potential pathogenic variants in subjects under 65 years old with very severe or fatal COVID‑19 Other
2022-06-21
EGAS00001006373 Longitudinal ctDNA in Uveal Melanoma Other
2022-06-21
EGAS00001006374 Pathogenic variants damage cell compositions and single cell transcription in cardiomyopathies Other
2022-06-22
EGAS00001006375 An Atlas of Cells in the Human Tonsil Other
2022-06-22
EGAS00001006376 SARS-CoV-2 host genetics and COVID-19 outcomes in admixed Brazilians with extreme phenotypes Other
2022-06-22
EGAS00001006377 Plasma whole genome sequencing from patients with stage IV colorectal cancer and microsatellite instability Other
2022-06-22
EGAS00001006378 Whole genome landscape of 25 metastatic cutaneous squamous cell carcinoma cSCC patients Other
2022-06-23
EGAS00001006380 Bulk-tissue RNA-sequencing paired nuclear and cytoplasmic fractions of anterior prefrontal cortex, cerebellar cortex and putamen tissues from post-mortem neuropathologically-confirmed control individuals. Other
2022-06-28
EGAS00001006381 HSP90 inhibitor resistant cell line Other
2022-06-28
EGAS00001006383 Exome & MiSeq sequencing of individuals with Huntington's disease Other
2022-06-28
EGAS00001006385 CNV profile in HSP90 inhibitor resistant K562 cells Other
2022-06-29
EGAS00001006388 Detection and genomic analysis of BRAF fusions in Juvenile Pilocytic Astrocytoma through the combination and integration of multi-omic data Other
2022-06-30
EGAS00001006392 Single-cell study of 14 childhood medulloblastoma patients Whole Genome Sequencing
2022-07-01
EGAS00001006393 Homologous recombination deficiency derived from whole-genome sequencing predicts platinum response in triple-negative breast cancers Other
2022-07-01
EGAS00001006394 Chromatin accessibility changes in hiPSC-derived neurons after BDNF and KCl stimulations Other
2022-07-01
EGAS00001006395 Quantitative Exploratory Proteomics Analysis of Glioblastoma in Initial and Recurrent Tumors Other
2022-07-01
EGAS00001006396 CD8+ Tumor-Infiltrating Lymphocyte Abundance is a Positive Prognostic Indicator in Nasopharyngeal Cancer Other
2022-07-04
EGAS00001006398 Multi-omics analyses of airway host-microbe interactions in chronic obstructive pulmonary disease identify potential therapeutic interventions Other
2022-07-04
EGAS00001006400 Molecular profiling of EBV associated diffuse large B-cell lymphoma Other
2022-07-05
EGAS00001006401 Study of the microenvironment of angioimmunoblastic T-cell lymphoma Cancer Genomics
2022-07-06
EGAS00001006404 Sex chromosome aneuploidies give rise to changes in the circular RNA profile Other
2022-07-07
EGAS00001006406 DNA methylation-based prognostic subtypes of chordoma tumors in tissue Other
2022-07-07
EGAS00001006408 Genomic landscape and molecularly-informed therapy in thymic carcinoma and other advanced thymic epithelial tumors (H021, HIPO) Other
2022-07-08
EGAS00001006410 RNA sequencing data of 142 samples from 142 patients with HER2+ breast cancer treated with letrozole or tamoxifen (SOLTI PAMELA trial) Other
2022-07-08
EGAS00001006411 Induction Failure in Childhood and Young Adult T-cell Acute Lymphoblastic Leukemia Cancer Genomics
2022-07-08
EGAS00001006417 INDIA Other
2022-07-11
EGAS00001006419 Repurposing azacitidine and carboplatin to prime immune checkpoint blockade-resistant melanoma for anti-PD-L1 re-challenge Other
2022-07-12
EGAS00001006420 Repurposing azacitidine and carboplatin to prime immune checkpoint blockade-resistant melanoma for anti-PD-L1 re-challenge Other
2022-07-12
EGAS00001006421 Cystic fibrosis multi-omics study Other
2022-07-12
EGAS00001006422 Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities Other
2022-07-12
EGAS00001006423 GWAS genotype data of Japanese Other
2022-07-13
EGAS00001006425 Prostate cancer ancestral genomic disparity Other
2022-07-13
EGAS00001006427 Dataset with genome-wide array data from 64 Tunisian and 45 Moroccan individuals. Other
2022-07-13
EGAS00001006428 Palbociclib resistance analyses on breast cancer bone metastasis PDX Other
2022-07-13
EGAS00001006429 Analyses of IACS-010759 treatment resistance on breast cancer bone metastases Other
2022-07-13
EGAS00001006431 Whole exome-sequencing of pediatric and adult H3-K27M diffuse midline glioma Other
2022-07-15
EGAS00001006432 Malignant mesothelioma EWAS on European prospective study Epigenetics
2022-07-15
EGAS00001006433 ctDNA quantification in Ewing sarcoma patients Other
2022-07-16
EGAS00001006434 Exploring germline and somatic mutagenesis in the extended family with germline pathogenic variant in POLD1 Other
2022-07-18
EGAS00001006439 Copy Number Variation using Affymetrix Optima Array Other
2022-07-18
EGAS00001006440 Genetic regulation of RNA splicing in human pancreatic islets Other
2022-07-18
EGAS00001006441 Transcriptome profiling of three giant cell tumour of bone cell lines Other
2022-07-19
EGAS00001006442 Time-dependent characterization of CNS response in COVID-19 Other
2022-07-19
EGAS00001006444 Airway Dysbiosis Accelerates Lung Function Decline in Chronic Obstructive Pulmonary Disease Other
2022-07-19
EGAS00001006445 T cell reactivity of MHC epitopes Other
2022-07-21
EGAS00001006452 WGS of PMBCL Cancer Genomics
2022-07-22
EGAS00001006453 Whole-Exome Sequencing analyses in tamoxifen-associated endometrial cancer Other
2022-07-22
EGAS00001006456 Genomic analysis and evolutionary modeling of breast and larynx cancer, based on specimens from Polish population Other
2022-07-23
EGAS00001006457 Chromatin activation profiling of stereotyped chronic lymphocytic leukemias reveals a subset #8 specific signature Other
2022-07-25
EGAS00001006459 Case Report: early contribution of germline and nevi genetic alterations to a rapidly-progressing Cutaneous Melanoma Patient Exome Sequencing
2022-07-25
EGAS00001006460 RaScALL: Rapid screening of RNA-seq in acute lymphoblastic leukaemia Other
2022-07-26
EGAS00001006461 High-resolution lung adenocarcinoma expression subtypes identify tumors with dependencies on MET, CDK4, CDK6, and PD-L1 Other
2022-07-26
EGAS00001006462 Multimodal Epigenetic Sequencing Analysis (MESA) of Cell-free DNA for Non-invasive Cancer Detection Other
2022-07-27
EGAS00001006463 in silico drug target prediction for melanoma Other
2022-07-27
EGAS00001006464 Colorectal cancer transcriptomics with primary and metastatic samples Other
2022-07-27
EGAS00001006465 Colorectal cancer genomics with primary and metastatic samples Other
2022-07-27
EGAS00001006466 Multi-focal genomic dissection of synchronous primary and metastatic tissue from de novo metastatic prostate cancer Other
2022-07-27
EGAS00001006468 OAC RNASeq Other
2022-07-28
EGAS00001006469 OAC scRNASeq Other
2022-07-28
EGAS00001006470 OAC WGS Other
2022-07-28
EGAS00001006472 Multiple Tissue Monitoring in Huntington disease - RNAseq fibroblasts Other
2022-07-29
EGAS00001006473 Multiple Tissue Monitoring in Huntington disease - RNAseq adipose tissue Other
2022-07-29
EGAS00001006474 Multiple Tissue Monitoring in Huntington disease - RNAseq skeletal muscle Other
2022-07-29
EGAS00001006477 The HLA ligandome of oropharyngeal squamous cell carcinomas reveals shared tumor-exclusive peptides for semi-personalized vaccination Other
2022-07-29
EGAS00001006478 Tumor microenvironment study of ovarian granulosa cell tumors Other
2022-07-29
EGAS00001006479 Comprehensive de novo variant discovery with HiFi long-read sequencing Other
2022-07-30
EGAS00001006486 Blina_Tumour_project Whole Genome Sequencing
2022-08-03
EGAS00001006487 Characterization of Arabian Peninsula whole exomes Other
2022-08-04
EGAS00001006488 SPECIAL: Dissecting the melanoma ecosystem one cell at the time during immunotherapy Other
2022-08-05
EGAS00001006489 Colorectal cancer study Other
2022-08-05
EGAS00001006490 Somatic copy number alteration and fragmentation analysis in circulating tumor DNA for cancer screening and treatment monitoring in colorectal cancer patients Other
2022-08-05
EGAS00001006491 Control of Focal Adhesion Kinase Activation by RUNX1-regulated miRNAs in high-risk AML Other
2022-08-06
EGAS00001006492 RNAseq analysis on metastatic Colorectal Cancer xenografts samples RNASeq
2022-08-08
EGAS00001006494 TRACERx NSCLC - Whole exome multiregion sequencing data Exome Sequencing
2022-08-09
EGAS00001006495 Upper cortical layer-driven network impairment in schizophrenia Other
2022-08-09
EGAS00001006497 Bulk RNA-seq of stromal cells from multiple cancer types Other
2022-08-10
EGAS00001006498 Finding structural variation from the human skin fibroblast at the single-cell level Other
2022-08-10
EGAS00001006499 The Extracellular RNA Quality Control (exRNAQC) study (phase 2) RNASeq
2022-08-11
EGAS00001006502 Immune microenvironment and lineage tracing help deciphering Rosette-forming GlioNeuronal Tumors: a multi-omic analysis of 9 cases Other
2022-08-12
EGAS00001006503 Histone modifications of cfDNA Epigenetics
2022-08-15
EGAS00001006510 Reliable assessment of telomere maintenance mechanisms in neuroblastoma Other
2022-08-17
EGAS00001006511 ATAC-Seq on OCIAML-22 Fractions Other
2022-08-17
EGAS00001006512 RNA-Seq on OCIAML-22 Fractions Other
2022-08-17
EGAS00001006513 Whole Genome Sequencing on OCIAML-22 Other
2022-08-17
EGAS00001006517 Multi-region RNA sequencing of tumour regions and tumour-adjacent normal lung tissue Other
2022-08-19
EGAS00001006518 Gene signature for predicting homologous recombination deficiency in triple-negative breast cancer Other
2022-08-19
EGAS00001006519 Genetic variants of the COL4A3, COL4A4, and COL4A5 genes contribute to thinned glomerular basement membrane lesions in sporadic IgA nephropathy patients Other
2022-08-22
EGAS00001006520 ATAC-seq/ChIP part Other
2022-08-22
EGAS00001006521 RNA-seq SE Other
2022-08-22
EGAS00001006522 RNA-seq PE Other
2022-08-22
EGAS00001006523 RRBS data from TRACERx non-small cell lung cancer (NSCLC) tumours and matched normal adjacent tissue. Other
2022-08-22
EGAS00001006526 Paired WGS data from Wilms Tumors Other
2022-08-23
EGAS00001006527 Characterization of Leukemic Stem Cells in DNMT3Amut and NPM1mut AMLs Other
2022-08-23
EGAS00001006528 Renal Cell Carcinoma Tumors From S-TRAC trial (NCT00375674) Whole Transcriptome Sequencing Other
2022-08-23
EGAS00001006529 Renal Cell Carcinoma Tumors From S-TRAC trial (NCT00375674) Exome Sequencing Other
2022-08-23
EGAS00001006530 Complex patterns of genomic heterogeneity identified in 42 tumor samples and ctDNA of a pulmonary atypical carcinoid patient Cancer Genomics
2022-08-23
EGAS00001006531 Bulk RNA data from Wilms Tumors Other
2022-08-24
EGAS00001006532 Somatic Inactivation of Breast Cancer Predisposition Genes in Tumours Associated with Pathogenic Germline Variants Other
2022-08-24
EGAS00001006533 Neuroblastoma Evolution Other
2022-08-24
EGAS00001006534 Single-cell RNA-seq of human kidney tumors Other
2022-08-25
EGAS00001006535 Characterizing the tumor immune microenvironment of ependymomas using targeted gene expression profiles and RNA-sequencing the pros and cons Other
2022-08-25
EGAS00001006537 single nuclei RNASeq of 5 regions of the human prenatal brain Other
2022-08-25
EGAS00001006538 Single-cell multi-omics of relapse/refractory multiple myeloma patients (Hipo K08K/H067/K43R) Other
2022-08-26
EGAS00001006539 cfDNA in Hereditary And High-Risk Malignancies (CHARM) Other
2022-08-26
EGAS00001006540 Robust methylation-based classification of brain tumours using nanopore sequencing Other
2022-08-28
EGAS00001006542 Significant and pervasive effects of RNA degradation on Nanopore direct RNA sequencing Other
2022-08-29
EGAS00001006545 Duplexseq_of_the_interstrand_crosslinks_WGS Other
2022-08-30
EGAS00001006547 A catalog of the genetic causes of Hereditary Angioedema in the Canary Islands (Spain) Other
2022-08-30
EGAS00001006551 Adult human kidney organoids originate from CD24+ cells and represent an advanced model for adult polycystic kidney disease Other
2022-08-31
EGAS00001006552 Synthetic genotypes and phenotypes of 500.000 individuals Other
2022-09-01
EGAS00001006553 Integrative modeling of tumor genomes and epigenomes for enhanced cancer diagnosis by cell-free DNA. Other
2022-09-01
EGAS00001006554 A living biobank of patient-derived ductal carcinoma in situ Mouse-INtraDuctal xenografts identifies factors associated with risk of invasive progression Other
2022-09-02
EGAS00001006555 Ovarian carcinosarcoma genomics and eribulin response Other
2022-09-05
EGAS00001006557 Sequencing Data of HGSC patient-derived cell lines and organoids Cancer Genomics
2022-09-05
EGAS00001006558 H3Africa - Kidney Disease Research Network Other
2022-09-05
EGAS00001006559 Single-cell ATAC-seq analysis for COVID19 patients Other
2022-09-05
EGAS00001006560 Single-cell RNA-seq analysis for COVID19 patients Other
2022-09-05
EGAS00001006563 Single cell transcriptome profiling of childhood soft tissue sarcomas Other
2022-09-05
EGAS00001006565 Hematopoietic differentiation at single-cell resolution in NPM1-mutated AML Other
2022-09-05
EGAS00001006567 Deciphering somatic mosaic structural variation in human blood lineages using single-cell multiomics Other
2022-09-06
EGAS00001006572 HSC_colony_many_years_post_allogeneic_bone_marrow_transplant___Bait_set_3 Other
2022-09-06
EGAS00001006573 Longitudinal monitoring of cell-free DNA methylation in ALK-positive non-small cell lung cancer patients Other
2022-09-06
EGAS00001006574 Erasmus MC COVID-19 cohort-associated connected datasets study Other
2022-09-06
EGAS00001006575 Whole-genome sequencing in gastric cancer (part2) Other
2022-09-07
EGAS00001006576 Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signatures Other
2022-09-07
EGAS00001006577 The genomic landscape of acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21 Other
2022-09-07
EGAS00001006582 Whole transcriptome profiling of liquid biopsies from tumour xenografted mouse models: validation cohort Other
2022-09-08
EGAS00001006583 RNAseq of liver harvested from CDAHFD mice treated for 8 weeks with either the MGAT2 inhibitor compound BMS-963272 or vehicle Other
2022-09-08
EGAS00001006584 RNAseq of jejunum (small intestine) harvested from CDAHFD mice treated for 8 weeks with either the MGAT2 inhibitor compound BMS-963272 or vehicle Other
2022-09-08
EGAS00001006585 Somatic mutations predict an aggressive phenotype in meningioma but do not drive grade progression Other
2022-09-09
EGAS00001006591 Real-time analysis of the cancer genome and fragmentome from plasma and urine short and long cell-free DNA using Nanopore sequencing Other
2022-09-09
EGAS00001006593 Whole-Transcriptomic Profiling of Sorted Human Renal Cell Carcinoma Immune Populations Other
2022-09-09
EGAS00001006594 RNA sequencing of AD, MCI and control ONS cells RNASeq
2022-09-12
EGAS00001006595 High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform, P49-P104 and run1 replicates Other
2022-09-12
EGAS00001006596 Transcriptomic profiles of chronic lymphocytic leukemia before and after frontline therapy: 5-year results from the randomized CLL14 study Other
2022-09-13
EGAS00001006598 Treatment-mediated selection of lethal prostate cancer clones defined by copy number architectures Other
2022-09-14
EGAS00001006599 Defective homologous recombination in HCC Other
2022-09-14
EGAS00001006600 Genomic landscape of DS-ALL Cancer Genomics
2022-09-14
EGAS00001006601 Cetuximab treatment of metastasis-derived organoids (LMO) RNASeq
2022-09-15
EGAS00001006602 HLF COPD Transcriptomics Other
2022-09-15
EGAS00001006603 HLF COPD DNA Methylomics Epigenetics
2022-09-15
EGAS00001006604 Hi-C analysis of metastatic prostate tumors Other
2022-09-15
EGAS00001006605 DNA and RNA sequencing data from Ovarian Carcinosarcoma patients from the Glasgow Cohort. Other
2022-09-15
EGAS00001006609 Long-read sequencing for cell-free DNA analysis (human pacbio) Other
2022-09-19
EGAS00001006610 The clinical utility of genomics in childhood cancer extends beyond targetable mutations - WGS data Other
2022-09-19
EGAS00001006612 Hi-C analysis of metastatic prostate tumors - Part 2 Other
2022-09-19
EGAS00001006613 Tumorigenic role of Musashi-2 in aggressive mantle cell lymphoma Other
2022-09-20
EGAS00001006614 Adaptive single-KIR+NKG2C+ NK cells expanded from superdonors show potent missing-self reactivity and efficiently control HLA-mismatched acute myeloid leukemia RNASeq
2022-09-20
EGAS00001006617 microRNA and isomiR profiling of Stage 1 epithelial ovarian carcinoma Other
2022-09-21
EGAS00001006621 Genetic characterization patients affected by Cancer of Unknown Primary Other
2022-09-22
EGAS00001006629 Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signatures (Hipo_021) Other
2022-09-23
EGAS00001006631 The Genetic Landscape of Ocular Adnexa MALT Lymphoma Reveals Frequent Aberrations in NFAT and MEF2B Signaling Pathways Other
2022-09-26
EGAS00001006632 Nasal epithelial cells of PCD and non-PCD patients grown at air-liquid interface for RNAseq analysis Other
2022-09-27
EGAS00001006633 Identification of neoantigen from MSI-CRC patient derived organoids and its application for targeting by autologous T cells Other
2022-09-27
EGAS00001006642 The clinical utility of genomics in childhood cancer extends beyond targetable mutations - Cancer Panel data Other
2022-09-28
EGAS00001006643 Capturing sex-specific and infertility-linked effects of assisted reproductive technologies on the cord blood DNA methylome Other
2022-09-28
EGAS00001006644 Multi-organ landscape of therapy-resistant melanoma Other
2022-09-29
EGAS00001006645 H3Africa - Trauma And Neurobiology: Maternal stress and transgenerational impact. Search for Epigenetic Markers Other
2022-09-29
EGAS00001006646 Follicular Lymphoma Whole Genome and Transcriptome Sequencing Cancer Genomics
2022-09-29
EGAS00001006648 Integrative pan-cancer genomic and transcriptomic analyses of refractory metastatic cancer Other
2022-09-30
EGAS00001006649 UCSF WCDT WGS/WGBS mCRPC Other
2022-09-30
EGAS00001006651 Germline sequencing Other
2022-10-02
EGAS00001006652 Intratumoral Heterogeneity and Clonal Evolution Induced by HPV Integration. Other
2022-10-02
EGAS00001006653 Whole genome analysis of pediatric patients with medulloblastoma Other
2022-10-03
EGAS00001006656 Exome sequencing from cfDNA blood samples. 159 samples at 2x101bp Illumina reads in Fastq format. Other
2022-10-03
EGAS00001006657 Nasal brushes analysis Other
2022-10-03
EGAS00001006659 Gene copy number variation in pediatric mental illness in a general population Other
2022-10-03
EGAS00001006660 Persistent Mutation Burden Drives Sustained Anti-Tumor Immune Responses Other
2022-10-03
EGAS00001006661 scRNA-seq of patient-derived PDAC organoids and matched CAFs Other
2022-10-03
EGAS00001006663 BinDel: software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples Other
2022-10-04
EGAS00001006665 single-cell RNA-Seq of colorectal cancer patient samples Transcriptome Analysis
2022-10-05
EGAS00001006666 bulk RNA-Seq of colorectal cancer patient samples RNASeq
2022-10-05
EGAS00001006670 DNA methylation landscape of prostate cancer Other
2022-10-07
EGAS00001006674 Follicular lymphoma at diagnosis, treated in first line with immunochemotherapy Other
2022-10-10
EGAS00001006675 T cell responses of ALS patients Other
2022-10-10
EGAS00001006678 Longitudinal evaluation of serum microRNAs as biomarkers for neuroblastoma burden and therapeutic p53 reactivation Other
2022-10-10
EGAS00001006679 Identification of genomic aberrations in low-grade serous ovarian cancer Other
2022-10-10
EGAS00001006680 Advanced molecular neuropathology to increase diagnostic accuracy in pediatric neurooncology Other
2022-10-12
EGAS00001006683 Res1_H23_exp2_MC_13_07_22 Other
2022-10-12
EGAS00001006688 Tocilizumab treatment leads to early resolution of myeloid dysfunction and lymphopenia in patients hospitalized with COVID-19 Other
2022-10-13
EGAS00001006689 Genomic and ecologic characteristics of the airway microbial-mucosal complex Other
2022-10-13
EGAS00001006690 RNA seq before and after cold pressor test Other
2022-10-13
EGAS00001006692 Pre-neoplastic liver colonization by 11p15.5 altered mosaic cells in young children with hepatoblastoma Other
2022-10-13
EGAS00001006693 Whole Genome Sequences of 18th century African descended individuals from Charleston, South Carolina. Other
2022-10-13
EGAS00001006694 Single-cell atlas of multiple myeloma and precursor diseases Other
2022-10-14
EGAS00001006695 Tissue DNA, WBC DNA and cfDNA (deep-)sequencing of mCRC patients treated with doublet chemotherapy and anti-EGFR in the CAIRO5 study Other
2022-10-17
EGAS00001006696 Shallow sequencing of organoid/xenograft or human colorectal metastases Whole Genome Sequencing
2022-10-17
EGAS00001006697 Targeted Sequencing Xenturion Exome Sequencing
2022-10-17
EGAS00001006698 Characterization of chromatin accessibility in metastatic prostate cancer Other
2022-10-17
EGAS00001006700 Plasma DNA end analysis (mouse) Other
2022-10-18
EGAS00001006701 Cell-free DNA cleavages analysis (human) Other
2022-10-18
EGAS00001006702 Characterization of MCSP+ melanoma DCC and MelDCC lines Other
2022-10-19
EGAS00001006703 High-resolution testing of ctDNA dynamics predicts survival in metastatic NSCLC Other
2022-10-20
EGAS00001006704 Whole blood transcriptomic analysis of ANCA-associated vasculitis Other
2022-10-20
EGAS00001006705 Germline sequencing Other
2022-10-20
EGAS00001006706 Proteogenomic analysis reveals RNA as a source for tumor-agnostic neoantigen identification (H021) Other
2022-10-21
EGAS00001006707 The University of Hong Kong Colon Cancer GCV Study Other
2022-10-21
EGAS00001006710 Genomic profiling of subcutaneous patient derived xenograft models of solid childhood cancer Cancer Genomics
2022-10-21
EGAS00001006711 Hexanucleotide repeat expansions in C9orf72 alter microglial responses and prevent a coordinated glial reaction in ALS Other
2022-10-22
EGAS00001006712 DNA methylation-based classification of sinonasal tumors [Proteomics data] Other
2022-10-23
EGAS00001006713 DNA methylation-based classification of sinonasal tumors [DNA sequencing] Other
2022-10-23
EGAS00001006716 A single-cell transcriptional gradient in human cutaneous memory T cells restricts Th17/Tc17 identity Other
2022-10-26
EGAS00001006718 Test Study for EGA using data from 1000 Genomes Project - Big CRAM, BAM, VCF and BCF files used for testing Other
2022-10-28
EGAS00001006719 Whole genome sequencing of AVM endothelial and non-endothelial cell fractions Other
2022-10-28
EGAS00001006720 Sputum fungal microbiota in an overall healthy population in Guangdong province, China Other
2022-10-29
EGAS00001006721 Sputum bacterial microbiota in an overall healthy population in Guangdong province, China Other
2022-10-29
EGAS00001006723 Deconvolution of bulk RNA-Seq using single cell RNA-Seq Other
2022-10-31
EGAS00001006724 Comprehensive Whole-Genome Sequence Annotation to Resolve the Genetic Architecture of Cerebral Palsy Whole Genome Sequencing
2022-11-01
EGAS00001006725 Whole genome sequencing dataset of 200 trio families from the CHILD cohort study. Whole Genome Sequencing
2022-11-01
EGAS00001006727 Bulk RNAseq of mCRC organoids Other
2022-11-02
EGAS00001006728 Single cell RNA-sequencing of tissues from NSCLC patients treated with chemoimmunotherapy Transcriptome Analysis
2022-11-02
EGAS00001006729 Targeted sequencing of brain AVM tissues Other
2022-11-02
EGAS00001006730 Measurement of SARS-CoV-2 variants fraction in infected alveolar cells Other
2022-11-03
EGAS00001006731 WGS of CD138+ samples collected from MM patients Other
2022-11-03
EGAS00001006732 GENOMIC MUTATION LANDSCAPE OF SKIN CANCERS FROM DNA REPAIR-DEFICIENT XERODERMA PIGMENTOSUM PATIENTS Other
2022-11-03
EGAS00001006736 NIBIT-M4 Clinical Trial samples Other
2022-11-04
EGAS00001006739 Neoadjuvant Chemo or Combined Chemo-Radiation Therapy of Pancreatic Ductal Adenocarcinoma Yields Fundamentally Different Proteome Biology of the Residual Tumor Mass Other
2022-11-07
EGAS00001006741 Chromatin landscape of medulloblastoma reveals context dependent driver Other
2022-11-07
EGAS00001006744 Structural Expression of BMMF in tissues of colorectal, lung and pancreatic cancer patients Other
2022-11-08
EGAS00001006746 Human primary and metastatic colorectal cancer (CRC) samples RNASeq
2022-11-09
EGAS00001006747 Targeted therapy of advanced parathyroid carcinoma guided by genomic and transcriptomic profiling (hipo_021) Other
2022-11-09
EGAS00001006755 Human pan-cancer plasma cfRNA study - raw data Other
2022-11-10
EGAS00001006757 Enrichment of oral-derived bacteria in inflamed colorectal tumors and distinct associations of Fusobacterium in the mesenchymal subtype Other
2022-11-11
EGAS00001006758 The Iberian Roma genetic variant server Other
2022-11-11
EGAS00001006759 Neutrophil extracellular traps have auto-catabolic activity and produce mononucleosome-associated circulating DNA Whole Genome Sequencing
2022-11-13
EGAS00001006762 Single-cell transcriptomics identifies pathogenic T-helper 17.1 cells and pro-inflammatory monocytes in ICI-related pneumonitis Other
2022-11-14
EGAS00001006767 Data containing genome-wide SNP data from Northwestern Amazonia Other
2022-11-14
EGAS00001006769 BCR-ABL is enriched in S- and G2-cell cycle phases Other
2022-11-14
EGAS00001006771 RNA sequencing analyses of chronic lymphocytic leukemia (CLL) Transcriptome Analysis
2022-11-15
EGAS00001006772 S3 Swedish schizophrenia case-control study Population Genomics
2022-11-15
EGAS00001006775 Whole Genome Sequencing Data of High Grade Serous Ovarian Cancer Other
2022-11-16
EGAS00001006778 Multi-omics identify falling LRRC15 as a COVID-19 severity marker and persistent pro-thrombotic signals in convalescence Other
2022-11-17
EGAS00001006779 Host pathogen interaction long read transcriptome Other
2022-11-17
EGAS00001006780 Single-cell RNA and ATAC sequencing data analysis of human postmenopausal fallopian tube and ovary Other
2022-11-17
EGAS00001006781 Tertiary lymphoid structure signatures are associated with immune checkpoint inhibitor related acute interstitial nephritis Transcriptome Analysis
2022-11-17
EGAS00001006782 PDAC organoid genomic heterogeneity Other
2022-11-20
EGAS00001006784 Leukemia sequencing study Other
2022-11-21
EGAS00001006785 Integrative analysis of exome-seq, RNA-seq, ATAC-seq (bulk and single-cell), and Hi-C data generated from 3-D spatially mapped samples acquired during surgical resection from 10 patients diagnosed with IDH-WT glioblastoma Other
2022-11-21
EGAS00001006786 Frequencies of variants in the Danish population Whole Genome Sequencing
2022-11-22
EGAS00001006787 scRNAseq and scATACseq of placebo controlled-trial on MMR non-specific effects Other
2022-11-22
EGAS00001006788 Transcriptional_reprogramming_from_innate_immune_functions_to_a_pro_thrombotic_signature_upon_SARS_CoV_2_sensing_by_monocytes_in_COVID_19 Transcriptome Analysis
2022-11-22
EGAS00001006789 The molecular landscape of homologous recombination deficient, end-stage, high grade serous ovarian cancer Other
2022-11-23
EGAS00001006791 DNA methylation atlas of normal human cell types Other
2022-11-23
EGAS00001006793 Molecular heterogeneity and commonalities in pancreatic cancer precursors with gastric and intestinal phenotype Other
2022-11-23
EGAS00001006794 RNA-sequencing of ex vivo exhausted human antigen-specific T cells RNASeq
2022-11-23
EGAS00001006796 The genomic landscape of acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21 Other
2022-11-24
EGAS00001006800 Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line WXS Exome Sequencing
2022-11-28
EGAS00001006801 Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line WXS derived Other
2022-11-28
EGAS00001006802 Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line RNA-Seq RNASeq
2022-11-28
EGAS00001006803 Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line RNA-Seq derived RNASeq
2022-11-28
EGAS00001006805 Highly sensitive liquid biopsy Duplex sequencing complements tissue biopsy to enhance detection of clinically relevant genetic variants Other
2022-11-29
EGAS00001006807 Detection of isoforms and genomic alterations by high-throughput full-length single-cell RNA sequencing in HGSOC Other
2022-11-29
EGAS00001006808 Loss of LGR4/GPR48 causes severe neonatal salt-wasting due to disrupted WNT signaling altering adrenal zonation Other
2022-11-29
EGAS00001006811 Study of Korean Parkinson's disease Other
2022-11-30
EGAS00001006813 FFPE, buffycoat and cell free DNA from N. German esophagus cancer patients - 2021 Other
2022-11-30
EGAS00001006818 The impact of BNT162b2 mRNA vaccine against SARS-CoV-2 on adaptive and innate immune responses Other
2022-11-30
EGAS00001006819 Erythroid/megakaryocytic differentiation confers BCL-XL dependency and venetoclax resistance in acute myeloid leukemia Other
2022-11-30
EGAS00001006820 NPY methylated ctDNA is a promising biomarker for treatment response monitoring in metastatic colorectal cancer Cancer Genomics
2022-11-30
EGAS00001006821 Tumor educated platelets for BrCA RNASeq
2022-12-01
EGAS00001006823 Profiling of childhood neuroblastoma and the immune microenvironment by single-cell sequencing of RNA and TCR Other
2022-12-01
EGAS00001006826 Epigenome-wide association study of cocaine use disorder in postmortem human brain tissue Other
2022-12-01
EGAS00001006831 Dynamics of sequence and structural cell-free DNA landscapes in small-cell lung cancer Other
2022-12-01
EGAS00001006832 The role of MALT1 in driving IBN resistance in MCL Other
2022-12-01
EGAS00001006833 Malignant progression of an ancestral bone marrow clone harboring a CIC-NUTM2A fusion in isolated myeloid sarcoma Other
2022-12-02
EGAS00001006836 Single cell RNA sequencing of bone marrow mononuclear cells Other
2022-12-02
EGAS00001006838 Influence of Genomic Landscape on Cancer Immunotherapy for Newly Diagnosed Ovarian Cancer: Biomarker Analyses from the IMagyn050 Randomized Clinical Trial Other
2022-12-02
EGAS00001006843 TK-EPN862 - Patient-dervied xenograft model of Posterior Fossa A Ependymoma - WGS Cancer Genomics
2022-12-06
EGAS00001006844 TK-EPN862 - Patient-dervied xenograft model of Posterior Fossa A Ependymoma - RNAseq Other
2022-12-06
EGAS00001006845 The genome-wide mutational consequences of DNA hypomethylation Whole Genome Sequencing
2022-12-06
EGAS00001006847 scRNASeq of human innate lymphoid cells from different compartments Other
2022-12-06
EGAS00001006848 cfDNA dataset from extracelular vesicles and paired non-fractionated samples Other
2022-12-06
EGAS00001006851 Multiregion Whole Exome and Smart-Seq3 single cell RNA sequencing of Breast Tumors Other
2022-12-06
EGAS00001006855 Analyzing the expression profiles of genes in ureters with and without indwelling stents using RNAseq Other
2022-12-06
EGAS00001006856 Early on-treatment changes in circulating tumor DNA fraction and response to enzalutamide or abiraterone in metastatic castration-resistant prostate cancer Other
2022-12-07
EGAS00001006857 Rifaximin stimulates nitrogen detoxification by PXR-independent mechanisms in human small intestinal organoids Other
2022-12-07
EGAS00001006860 Exome sequencing of HCV+ lymphoma Other
2022-12-07
EGAS00001006864 T cell landscape definition by multi-omics identifies galectin-9 as novel immunotherapy target in chronic lymphocytic leukemia (CLL) Other
2022-12-08
EGAS00001006865 Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities WGS Other
2022-12-09
EGAS00001006866 Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities RNA-Seq Other
2022-12-09
EGAS00001006868 Smart-seq3 scRNA-seq of cells from primary (OV2295) and metastatic (OV2295R2) high-grade serous ovarian cancer cell-line Other
2022-12-12
EGAS00001006870 Population_based_analysis_of_POT1_variants_in_a_cutaneous_melanoma_case_control_cohort Other
2022-12-13
EGAS00001006871 RNAseq of paired primary and locally recurrent IDHwt GBM Other
2022-12-14
EGAS00001006873 Targeted DNA sequencing on 37 Merkel Cell Carcinomas from New Zealand with known Merkel cell polyomavirus status Other
2022-12-14
EGAS00001006874 WGS of MAPKi acquired resistant samples from patients and PDX models Other
2022-12-15
EGAS00001006879 Non-muscle Invasive Bladder Cancer Molecular Subtypes Predict Differential Response to Intravesical Bacillus Calmette-Guérin Other
2022-12-15
EGAS00001006881 Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities DNA-Methylation Other
2022-12-16
EGAS00001006883 ctDNA to predict risk of progression and death after trifluridin/tipiracil therapy Other
2022-12-16
EGAS00001006884 Molecular evolution of classic Hodgkin lymphoma revealed through whole genome sequencing of Hodgkin and Reed Sternberg cells Whole Genome Sequencing
2022-12-19
EGAS00001006885 Transcriptomic analysis of liver CD8+ T cells Other
2022-12-19
EGAS00001006886 One-step generation of tumor models by base editor multiplexing in adult stem cell-derived organoids Other
2022-12-20
EGAS00001006887 Chronic lymphocytic leukemia IGHV somatic hypermutation detection by targeted capture next-generation sequencing Other
2022-12-20
EGAS00001006894 Tracing early predictors of glioma evolution under therapy Other
2022-12-22
EGAS00001006898 Non-viral precision T cell receptor replacement for personalized cell therapy Other
2022-12-22
EGAS00001006902 PD-L1 blockade in combination with carboplatin as immune induction in metastatic lobular breast cancer: the GELATO-trial Other
2022-12-24
EGAS00001006903 Tracking the evolution of Therapy-Related Myeloid Neoplasms using chemotherapy signatures Other
2022-12-26
EGAS00001006904 Separation of chronic myeloid leukemia stem cells from normal hematopoietic stem cells at single-cell resolution Other
2023-01-03
EGAS00001006905 Mechanism of action and resistance to Trastuzumab Deruxtecan in patients with metastatic breast cancer: the DAISY trial Exome Sequencing
2023-01-04
EGAS00001006906 Genetic landscape of ENKTCL Cancer Genomics
2023-01-04
EGAS00001006907 germline variants in children with hematological cancer Other
2023-01-04
EGAS00001006908 IACS treatment on breast cancer bone metastases Other
2023-01-05
EGAS00001006909 Human leukocyte antigen alleles associate with COVID-19 vaccine immunogenicity and risk of breakthrough infection Other
2023-01-06
EGAS00001006910 Whole Exome and RNA sequencing of synchronous female bilateral breast cancers Cancer Genomics
2023-01-06
EGAS00001006911 The genomic diversity of Taiwanese Austronesian groups: implications for the ‘Into and Out of Taiwan’ models Population Genomics
2023-01-06
EGAS00001006913 Clinical utility of combined low-pass whole genome and targeted sequencing in liquid biopsies for diagnosis and monitoring of pediatric solid tumors Other
2023-01-09
EGAS00001006914 transcriptome analysis of NK cells sorted from PBMCs at baseline and after addition of a T cell dependent bispecific antibody (TDB) RNASeq
2023-01-09
EGAS00001006916 Vitamin C boosts DNA demethylation in TET2 germline mutation carriers Other
2023-01-10
EGAS00001006919 Genomic and epigenomic study of Japanese renal cell carcinoma including WGS, RNA-seq, ATAC-seq, and methyl-seq Other
2023-01-12
EGAS00001006920 van Hijfte GBM dataset 2022/A (single-nucleus RNA-seq) Other
2023-01-12
EGAS00001006923 Tracking early lung cancer metastatic dissemination in TRACERx using ctDNA Other
2023-01-13
EGAS00001006926 Blood transcriptome profiling links immunity to disease severity in myotonic dystrophy type 1 (DM1). Other
2023-01-16
EGAS00001006927 Genomic profiling of localized (lFL) and systemic follicular lymphoma (sFL) reveals novel insights into FL pathogenesis Other
2023-01-17
EGAS00001006928 Identifying rare genetic variants in 21 highly multiplex autism families Whole Genome Sequencing
2023-01-17
EGAS00001006929 CYP2C19 long-read sequencing Other
2023-01-17
EGAS00001006932 Multiome_HB Other
2023-01-17
EGAS00001006934 Isala Citizen Science Project: Cross-sectional branch Other
2023-01-17
EGAS00001006935 Bolleboom-Gao peri-tumoral snRNA-seq glioblastoma dataset 2022/A Other
2023-01-17
EGAS00001006937 TNBC ctDNA Targeted Panel Other
2023-01-18
EGAS00001006939 Multi-omic and functional analysis for classification and treatment of sarcomas with FUS-TFCP2 or EWSR1-TFCP2 fusions(H021/INF) Other
2023-01-19
EGAS00001006942 Clonal architecture and genomic features of smoking versus non-smoking oncogene-driven East-Asian non-small cell lung cancer Other
2023-01-20
EGAS00001006944 Genotype data from 'Dense sampling of ethnic groups within African countries reveals fine-scale genetic structure and extensive historical admixture.' Other
2023-01-20
EGAS00001006945 Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis Other
2023-01-20
EGAS00001006946 Genomic Analysis of a Metastatic Fusion-negative Embryonal Rhabdomyosarcoma Cancer Genomics
2023-01-20
EGAS00001006947 Case Report: Rare IKZF1 gene fusions identified in neonate with congenital KMT2A-rearranged Acute Lymphoblastic Leukemia Other
2023-01-22
EGAS00001006949 Pre-diagnostic saliva microbiota of Finnish children with autoimmune diseases Other
2023-01-23
EGAS00001006950 Genotype data of Japanese Other
2023-01-24
EGAS00001006951 Lung Adenocarcinoma Promotion by Air Pollutants Other
2023-01-24
EGAS00001006952 The immunological characterization of expanded tumor-infiltrating lymphocytes in renal cell carcinoma patients Other
2023-01-24
EGAS00001006954 Single-cell sequencing of adipose-derived mesenchymal stromal cells and dermal fibroblasts Transcriptome Analysis
2023-01-25
EGAS00001006958 The multifaceted genomic history of Ashaninka from Amazonian Peru Other
2023-01-26
EGAS00001006959 PELICAN45 RNAseq Dataset Other
2023-01-27
EGAS00001006960 The effector program of human CD8 T cells can promote both target cell killing and tissue remodeling Transcriptome Analysis
2023-01-28
EGAS00001006962 Clonal dynamics of normal hepatocyte expansions in homeostatic human livers and their association with the biliary epithelium Other
2023-01-31
EGAS00001006963 GCparagon: Evaluation and correction of GC biases in cell-free DNA at the fragment level Other
2023-02-01
EGAS00001006964 A novel Patient-Derived 3D Model Recapitulates Mantle Cell Lymphoma Lymph Node Signaling, Immune Profile and in vivo Ibrutinib Responses Other
2023-02-01
EGAS00001006965 Chronic lymphocytic leukemia patient-derived xenografts recapitulate clonal evolution to Richter transformation Other
2023-02-01
EGAS00001006966 RNA-seq on bronchial brushings collected in controlled human exposure to diesel exhaust Other
2023-02-01
EGAS00001006967 Personalized Onco-Genomic Project for pediatric and adolescent patients in British Columbia Other
2023-02-01
EGAS00001006968 Longitudinal peripheral blood DNA methylation profiling of endoscopic response to tofacitinib in moderate-to-severe ulcerative colitis patients Epigenetics
2023-02-02
EGAS00001006970 Single-cell RNA-seq and spatial transcriptomics data for the sarcoidosis baseline project Other
2023-02-02
EGAS00001006973 Treated and control Patient Derived Xenografts of colorectal cancer (CRC) samples RNASeq
2023-02-02
EGAS00001006975 A capture-based next-generation sequencing panel for the molecular characterization of chronic lymphocytic leukemia Cancer Genomics
2023-02-02
EGAS00001006976 B Cell Receptor Study From Metastatic Breast Cancer Tumour Samples Other
2023-02-02
EGAS00001006977 NanoString nCounter® PanCancer IO 360™on anti-PD1/anti-PD1+CTLA4 in patients with metastatic melanoma Other
2023-02-03
EGAS00001006978 Exome_sequencing_of_UK_Birth_Cohorts___Born_in_Bradford Other
2023-02-06
EGAS00001006980 scRNA-seq of total bone marrow mononuclear cells and CD3+ T cells of multiple myeloma patients and healthy donors Other
2023-02-06
EGAS00001006981 HLA-DR is absent in primitive macrophages through epigenetic silencing of master regulator CIITA Other
2023-02-06
EGAS00001006982 Diet driven microbial ecology underpins associations between cancer immunotherapy outcomes and the gut microbiome Other
2023-02-06
EGAS00001006983 Study of complex rearrangements and mutational signatures in neuroblastoma heterogeneous risk groups. Other
2023-02-07
EGAS00001006984 RNA sequencing of CCO- and CCO+ human hepatocytes Other
2023-02-07
EGAS00001006988 Multiomic Sequencing of Paired Primary and Metastatic Small Bowel Carcinoids Other
2023-02-08
EGAS00001006989 Pharmacogenomic profiling reveals molecular features of chemotherapy resistance in IDH wild type primary glioblastoma Other
2023-02-08
EGAS00001006990 A single cell view on host immune transcriptional response to in vivo BCG-induced trained immunity Transcriptome Analysis
2023-02-08
EGAS00001006992 Molecular analysis of cancer genomes in children with Lynch syndrome: exploring causal associations Other
2023-02-09
EGAS00001006994 Single cell multi-omic study of H3-K27M mutant diffuse midline glioma across age and location Other
2023-02-09
EGAS00001006995 Germline variants in childhood cutaneous melanoma Exome Sequencing
2023-02-10
EGAS00001006999 PhIP-Seq LLD Other
2023-02-13
EGAS00001007001 Biomarker Screen for Efficacy of Oncolytic Virotherapy in Patient-derived Pancreatic Cancer Cultures Other
2023-02-14
EGAS00001007002 Myeloid-specific KDM6B inhibition sensitizes Glioblastoma to PD1 blockade Other
2023-02-15
EGAS00001007003 Relevance of TMPRSS2, CD163/CD206 and CD33 in clinical severity stratification of COVID-19 Other
2023-02-15
EGAS00001007004 CAGEKID: Cancer Genomics of the Kidney - Targeted Sequencing Other
2023-02-15
EGAS00001007006 A machine learning classifier for DNA repair defects using plasma DNA Cancer Genomics
2023-02-15
EGAS00001007008 Quantitative analysis of a novel DNA hypermethylation panel for lung cancer diagnosis Epigenetics
2023-02-16
EGAS00001007011 Genome wide variation in the Angolan Namib desert reveals unique Pre-Bantu ancestry Other
2023-02-17
EGAS00001007013 NEC Other
2023-02-17
EGAS00001007014 Whole genome, RNA-seq and single-cell Multiome profile of multiple myeloma Cancer Genomics
2023-02-20
EGAS00001007016 Neuroblastoma heterogeneity Other
2023-02-20
EGAS00001007019 Neuroblastoma heterogeneity Other
2023-02-21
EGAS00001007021 Single-cell dissection of the immune response after a myocardial infarction Transcriptome Analysis
2023-02-21
EGAS00001007022 Covid19 RNAseq Fastq files Other
2023-02-21
EGAS00001007023 Integrated single cell analysis in transformed follicular lymphoma Other
2023-02-21
EGAS00001007024 RNAseq analysis on metastasis-derived organoids (LMO) RNASeq
2023-02-22
EGAS00001007025 Shot-gun stool metagenomics and colorectal cancer risk. Other
2023-02-22
EGAS00001007026 Parallel sequencing of extrachromosomal circular DNAs and transcriptomes in single cancer cells Cancer Genomics
2023-02-22
EGAS00001007027 Reconstruction of the personal information from human genome reads in gut metagenome sequencing data Other
2023-02-23
EGAS00001007029 A novel transcriptional signature identifies T-cell infiltration in high-risk paediatric cancer Other
2023-02-24
EGAS00001007033 A PROSTATE TUMORGRAFT PANEL TO ACCELERATE PRECISION MEDICINE Other
2023-02-24
EGAS00001007035 Single cell epigenomic study of H3-K27M mutant diffuse midline glioma across age and location Other
2023-02-24
EGAS00001007036 Whole-genome sequencing across 449 samples spanning 47 ethnolinguistic groups provides insights into genetic diversity in Nigeria Other
2023-02-24
EGAS00001007038 An IL-1β driven neutrophil-stromal cell axis fosters a BAFF-rich microenvironment in multiple myeloma Other
2023-02-26
EGAS00001007039 Molecular features of adenomas predicting metachronous colorectal cancer: a nested-case control study Other
2023-02-27
EGAS00001007041 IMI-RHAPSODY data Other
2023-02-27
EGAS00001007042 Methylation-based classification of human mesenchymal chondrosarcoma Other
2023-02-27
EGAS00001007044 Single-cell RNA-seq of cervix and placenta Other
2023-02-27
EGAS00001007045 Germline genome sequencing samples from the Hereditary Cancer Syndromes (ICCon) Cancer Flagship Other
2023-02-28
EGAS00001007047 VRK3 depletion in Pontine Diffuse Midline Glioma (DMG)-K27 altered cells RNASeq
2023-03-01
EGAS00001007048 Covid19 WGS BAM files Other
2023-03-01
EGAS00001007049 Genome-wide DNA Copy Number Analysis of high hyperdiploid acute lymphoblastic leukemia Cancer Genomics
2023-03-01
EGAS00001007050 Covid19 RNAseq BAM files Other
2023-03-01
EGAS00001007051 RNAseq analysis on primary sites Colorectal Cancer xenografts (PRX) samples RNASeq
2023-03-02
EGAS00001007052 Timing chromosomal amplification events using patterns of somatic mutations in high hyperdiploid acute lymphoblastic leukemia Other
2023-03-02
EGAS00001007053 Whole genome and whole exome sequencing of serial biopsies of relapsed/refractory diffuse large B-cell lymphoma. Whole Genome Sequencing
2023-03-02
EGAS00001007054 PhIP-Seq data Other
2023-03-03
EGAS00001007055 Single cell RNA-seq from AD and PS patients Other
2023-03-06
EGAS00001007057 Ultrasensitive detection of minor allele fractions in maternal samples based on microhaplotype analysis Other
2023-03-06
EGAS00001007059 cis-eQTL mapping of TB-T2D comorbidity in a five-way admixed SA cohort Other
2023-03-08
EGAS00001007060 RNA sequencing data of 257 samples from 106 patients with HR+/HER2- breast cancer treated with AC plus paclitaxel or letrozole plus ribociclib (SOLTI-1402 CORALLEEN trial) Other
2023-03-08
EGAS00001007061 Germline whole genome sequencing of patients with Li-Fraumeni syndrome Other
2023-03-08
EGAS00001007064 Linked-read based analysis of Medulloblastomas Other
2023-03-10
EGAS00001007066 Genomic determinants of therapy response in ETV6-RUNX1 leukemia Whole Genome Sequencing
2023-03-10
EGAS00001007067 Spatiotemporal Genomic Profiling of Intestinal Metaplasia Reveals Clonal Dynamics of Gastric Cancer Progression Other
2023-03-11
EGAS00001007070 RNA-seq of PDAC patient-derived xenograft tumors Transcriptome Analysis
2023-03-13
EGAS00001007071 cfDNAme allows early prediction of PE Other
2023-03-13
EGAS00001007072 LOGGIC Core BioClinical Data Bank: Added clinical value of RNA-Seq in an international molecular diagnostic registry for pediatric low-grade glioma patients Cancer Genomics
2023-03-13
EGAS00001007075 DNA methylation of peripheral blood leukocytes from patients with Li-Fraumeni syndrome Other
2023-03-13
EGAS00001007076 Treatment stratification and biomarker validation using patient-derived head and neck cancer organoids Other
2023-03-14
EGAS00001007077 ACT-Discover: identifying karyotype heterogeneity in pancreatic cancer evolution using ctDNA Other
2023-03-14
EGAS00001007078 Clonally resolved single-cell multi-omics identifies routes of cellular differentiation in acute myeloid leukemia Other
2023-03-14
EGAS00001007079 Transgenerational transmission of reproductive and metabolic dysfunction in the male progeny of polycystic ovary syndrome Other
2023-03-14
EGAS00001007080 Genetic heritage of the Baphuthi highlights an over-ethnicised notion of 'Bushman' in the Maloti-Drakensberg, southern Africa Other
2023-03-14
EGAS00001007081 PEACE melanoma 14 Other
2023-03-15
EGAS00001007082 Covid19 WGS Variant analysis Whole Genome Sequencing
2023-03-15
EGAS00001007083 Spatial transcriptomics reveal topological immune landscapes of Asian head and neck angiosarcoma Other
2023-03-16
EGAS00001007084 sWGS of Pap test smears from healthy donors and HGSOC patients and matched tumor tissue Other
2023-03-17
EGAS00001007085 Papua New Guinean Genome Altitude Project Population Genomics
2023-03-17
EGAS00001007086 The impact of mutational clonality in predicting the response to anti-PD-L1/PD-L1 in advanced urothelial cancer Other
2023-03-17
EGAS00001007087 Evolutionary landscape of clonal hematopoiesis in 3359 individuals from the general population Other
2023-03-17
EGAS00001007088 Nasal Polyp RNAsequencing, Skaraborg Sweden Other
2023-03-18
EGAS00001007089 Quantitative analysis of a novel DNA hypermethylation panel for lung cancer diagnosis using bronchial specimens Other
2023-03-18
EGAS00001007090 Point-of-care monitoring of head and neck cancer treatment response and recurrence development using nanopore-based ctDNA consensus sequencing Forensic or Paleo-genomics
2023-03-19
EGAS00001007091 Cell-to-cell variability in Myc dynamics drives transcriptional heterogeneity in cancer cells Other
2023-03-20
EGAS00001007092 Multiple Myeloma follow-up sequencing study Other
2023-03-20
EGAS00001007093 Long-term organoid culture of a small intestinal neuroendocrine tumor Other
2023-03-21
EGAS00001007094 Epigenetic landscape of mixed phenotype leukemias Other
2023-03-21
EGAS00001007095 BMP4 and temozolomide synergize in the majority of patient derived glioblastoma cultures Other
2023-03-21
EGAS00001007097 Gene expression profiles in paediatric ETV6-RUNX1 leukemia RNASeq
2023-03-21
EGAS00001007098 JAK/STAT signaling promotes the emergence of regenerative cell states in ulcerative colitis RNASeq
2023-03-21
EGAS00001007099 Implementation of pediatric precision oncology into clinical practice: The individualized Therapies for Children with cancer program “iTHER” Other
2023-03-21
EGAS00001007101 Cancer sequencing for somatic variant calling Other
2023-03-22
EGAS00001007103 Genomic profiling of Rare Tumors Other
2023-03-22
EGAS00001007104 Whole Exome Sequencing data of six chRCC tumors corresponding to three patients Other
2023-03-22
EGAS00001007105 Genomic Landscape of Follicular Lymphoma Across a Wide Spectrum of Clinical Behaviors Cancer Genomics
2023-03-22
EGAS00001007106 Covid19 WGS Raw Read files Other
2023-03-22
EGAS00001007108 Long-term organoid culture of a small intestinal neuroendocrine tumor rna-seq Other
2023-03-23
EGAS00001007110 Single-cell and bulk RNA-sequencing of nivolumab-treated glioblastoma Other
2023-03-23
EGAS00001007111 Genetic Determinants of Transcriptional Variation in Primary Human Monocytes Across Multiple Contexts Other
2023-03-23
EGAS00001007112 RNA stability controlled by m6A methylation contributes to X-to-autosome dosage compensation in mammals Other
2023-03-23
EGAS00001007113 TIGIT is the central player in T-cell suppression associated with CAR T-cell relapse in mantle cell lymphoma RNASeq
2023-03-23
EGAS00001007115 Effects of 2DG, Galactose, or Oligomycin on the epigenome remodeling induce by T cells activation. Other
2023-03-27
EGAS00001007116 Covid19 Transcriptomic Data analysis in Irish Population Other
2023-03-27
EGAS00001007117 Identification of Long Non-coding RNA Biomarker of Human Lupus Nephritis Disease Activity Other
2023-03-27
EGAS00001007118 Integrative genomic analyses in adipocytes implicate DNA methylation in human obesity and diabetes Other
2023-03-27
EGAS00001007119 RNA sequencing of a glioblastoma PDX cohort Other
2023-03-27
EGAS00001007120 Paired diagnostic and relapse medulloblastoma sequencing Other
2023-03-27
EGAS00001007124 RNA-Seq on GeparSixto tissue samples Other
2023-03-28
EGAS00001007125 T-cell receptor sequencing of tumor-infiltrating lymphocytes (TIL) in breast cancer Other
2023-03-28
EGAS00001007126 GM adipose tissue study Other
2023-03-29
EGAS00001007127 Human lymphoma plasma cfRNA - raw data Other
2023-03-30
EGAS00001007131 Archaeogenomic distinctiveness of the Isthmo-Colombian area Forensic or Paleo-genomics
2023-03-31
EGAS00001007136 T cell receptor repertoire sequencing reveals chemotherapy-driven clonal expansion in colorectal liver metastases Other
2023-03-31
EGAS00001007143 Persister cell phenotypes contribute to poor patient outcomes after neoadjuvant chemotherapy in PDAC (Hipo_015) Cancer Genomics
2023-04-03
EGAS00001007144 IL7-receptor expression is frequent in T-cell acute lymphoblastic leukemia and predicts sensitivity to JAK-inhibition Other
2023-04-03
EGAS00001007145 The Sys4MS cohort: a prospective cohort of patients with Multiple Sclerosis and omics Other
2023-04-03
EGAS00001007146 Molecular analysis of cancer genomes in children with Lynch syndrome: exploring causal associations Other
2023-04-04
EGAS00001007156 Cachexia - Non-Cachexia Metagenome Analysis Other
2023-04-07
EGAS00001007157 Elevated cfDNA after exercise is derived primarily from mature polymorphonuclear neutrophils, with a minor contribution of cardiomyocytes Epigenetics
2023-04-08
EGAS00001007159 Evaluation of triple negative breast cancer with heterogeneous immune infiltration Other
2023-04-11
EGAS00001007160 Exploring high-throughput drug sensitivity testing in neuroblastoma cell lines and patient-derived tumor organoids in the era of precision medicine Other
2023-04-12
EGAS00001007161 Neuroblastoma tumors by bulk RNAseq, from Berlanga et al, 2022 Other
2023-04-12
EGAS00001007162 A GWAS of Progression in Multiple Sclerosis Other
2023-04-12
EGAS00001007163 Oesophageal_Adenocarcinoma_Organoid_PacBio Cancer Genomics
2023-04-13
EGAS00001007164 Spatial and temporal intra-tumoural heterogeneity in advanced High-Grade Serous Ovarian Cancer: implications for surgical and clinical outcomes Other
2023-04-13
EGAS00001007165 RNAseq Other
2023-04-13
EGAS00001007166 ATACseq Other
2023-04-13
EGAS00001007167 Transcriptomic classes of BCR-ABL1 lymphoblastic leukemia Other
2023-04-13
EGAS00001007171 A Machine Learning Tool Integrating Circulating Cell-Free DNA Methylation with Clinical Variables for Non-Invasive Diagnosis of Liver Graft Pathology Other
2023-04-17
EGAS00001007172 Establishment and characterization of an Epstein-Barr virus-positive cell line from a non-keratinizing differentiated primary nasopharyngeal carcinoma Other
2023-04-18
EGAS00001007173 H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis Other
2023-04-18
EGAS00001007180 Chip_seq_oesophageal_adenocarcinoma_ Cancer Genomics
2023-04-18
EGAS00001007181 Primary_DIPG_expression_profiles Other
2023-04-18
EGAS00001007182 3D-GSC_expression_profiles Other
2023-04-18
EGAS00001007184 Accuracy and repeatability of epigenome-based signatures trained on Illumina MethylationEPIC BeadChip data Epigenetics
2023-04-18
EGAS00001007186 Structural variant analysis of homologous recombination-deficient genomes Other
2023-04-20
EGAS00001007187 RNA sequencing of primary B-cells infected with EBV virus RNASeq
2023-04-20
EGAS00001007189 HGSOC organoid sequencing study Cancer Genomics
2023-04-20
EGAS00001007192 Enhanced detection of MRD with cfDNA Fragmentomics. Cancer Genomics
2023-04-23
EGAS00001007194 Human liver NPCs single cell project Other
2023-04-23
EGAS00001007195 Developing somatic copy number and mutation calling tools for a bespoke sequencing platform Other
2023-04-24
EGAS00001007197 Monocyte Spike-in RNASeq Other
2023-04-24
EGAS00001007200 The genetic history of the southern Andes from present-day Mapuche ancestry Other
2023-04-26
EGAS00001007201 Methylation profiles in patients with blastic plasmacytoid dendritic cell neoplasm Other
2023-04-27
EGAS00001007204 Bacterial SNPs in the human gut microbiome associate with host BMI Other
2023-05-04
EGAS00001007205 RNA-Sequencing data of patient derived normal fibroblasts (NFs), cancer associated fibroblasts (CAFs) and tumor spheroid samples Other
2023-05-04
EGAS00001007210 Clinical Activity of Combined Telomerase Vaccination and Pembrolizumab in Advanced Melanoma: Results from a Phase I Trial Other
2023-05-05
EGAS00001007211 WGS Other
2023-05-06
EGAS00001007212 RNAseq Other
2023-05-06
EGAS00001007213 deep-learning-powered tissue deconvolution for cfDNA Other
2023-05-07
EGAS00001007216 TB-DAR Genotyping Study Other
2023-05-08
EGAS00001007217 Transcriptome analyses of a large cohort of adult B cell acute lymphoblastic leukemia samples Transcriptome Analysis
2023-05-08
EGAS00001007219 Digital tEchnology For Lung Cancer Treatment Other
2023-05-09
EGAS00001007220 Origination of Ovarian Cancer is Dependent on Specific Aneuploidy Landscape Cancer Genomics
2023-05-09
EGAS00001007221 RNAseq of Soft Tissue Sarcomas Other
2023-05-09
EGAS00001007222 Integrated genetic analysis of primary CNS lymphoma Cancer Genomics
2023-05-10
EGAS00001007223 Whole exome sequencing (WES) of previously untreated AML samples Other
2023-05-10
EGAS00001007227 Analysis of circulating miRNAs for the identification of new prognostic and predictive markers in gastro-entero-pancreatic neuroendocrine tumour (GEP-NET) RNASeq
2023-05-10
EGAS00001007229 A transcriptomic approach to understand patient susceptibility to pneumonia after abdominal surgery Other
2023-05-10
EGAS00001007230 Multiomic profiling of pleomorphic rhabdomyosarcoma Other
2023-05-10
EGAS00001007231 WGS of KCNQ2 R201C patient derived iPSC and its isogenic line Whole Genome Sequencing
2023-05-11
EGAS00001007235 Dataset with genome-wide array data from Algerian Amazigh (Chaoui and Mozabite) and non-Amazigh individuals Other
2023-05-14
EGAS00001007236 Whole-Exome Sequences from Imazighen and non-Imazghen from Algeria Other
2023-05-14
EGAS00001007237 Analysis of a cohort of familial ademomatous polyposis patients bearing APC gene mutation Other
2023-05-15
EGAS00001007238 cfDNA dataset from the urine supernatant of ovarian cancer patients and healthy controls Other
2023-05-15
EGAS00001007239 Genetic scoring guide for personalized risk assessment in pediatric B-cell precursor Acute Lymphoblastic Leukemia Other
2023-05-15
EGAS00001007240 Enhancer plasticity in endometrial tumorigenesis demarcates non-coding driver mutations and alterations in 3D genome organization to boost oncogene expression Cancer Genomics
2023-05-15
EGAS00001007241 Proteomic predictors of individualized nutrient-specific insulin secretion in health and disease RNASeq
2023-05-15
EGAS00001007242 Single-cell decoding of drug induced transcriptomic reprogramming in triple negative breast cancers Other
2023-05-16
EGAS00001007244 Genomic analyses to identify metabolic vulnerabilities Other
2023-05-16
EGAS00001007245 Pre-existing immunity drives the response to neoadjuvant chemotherapy in esophageal adenocarcinoma Other
2023-05-16
EGAS00001007248 Single molecule genome-wide mutation profiles of cell-free DNA for non-invasive detection of cancer Other
2023-05-16
EGAS00001007249 Whole genome sequencing of patients with or at risk for HCC Other
2023-05-16
EGAS00001007250 H3Africa - Genomic Characterization and Surveillance of Microbial Threats in West Africa Other
2023-05-17
EGAS00001007253 Clonal_selection_after_gene_therapy_in_SCD___Duplex_sequencing Cancer Genomics
2023-05-18
EGAS00001007254 Transcriptomics identifies blunted immunomodulatory effects of vitamin D in people with multiple sclerosis Other
2023-05-19
EGAS00001007255 Colon adenomas and adenocarcinomas and matched mucosae Other
2023-05-19
EGAS00001007257 Methylome profiling of epithelioid sarcoma Other
2023-05-20
EGAS00001007259 An isogenic human iPSC model unravels neurodevelopmental abnormalities in SMA Other
2023-05-22
EGAS00001007261 Spatial tumor microenvironment characterization and outcome of relapsed/refractory classic Hodgkin lymphoma Other
2023-05-23
EGAS00001007262 Gene expression of neutrophils in response to Mtb infection in persons living with HIV RNASeq
2023-05-23
EGAS00001007263 Cardiovascular disease biomarkers derived from circulating cell-free DNA methylation Other
2023-05-23
EGAS00001007286 Multi-omic analysis of the tumor microenvironment shows clinical correlations in Ph1 study of atezolizumab +/- SoC in MM Other
2023-05-26
EGAS00001007288 Comprehensive single-cell genome analysis at nucleotide resolution using the PTA Analysis Toolbox Other
2023-05-26
EGAS00001007290 Proteomic Analysis of Non-Muscle Invasive and Muscle Invasive Bladder Cancer Highlights Distinct Subgroups With Metabolic, Matrisomal, and Immune Hallmarks Other
2023-05-26
EGAS00001007291 Elucidating the heterogeneity of immunotherapy response and immune-related toxicities by longitudinal ctDNA and immune cell compartment tracking in lung cancer Cancer Genomics
2023-05-26
EGAS00001007292 The genomic landscape of recurrent ovarian high grade serous carcinoma: the BriTROC-1 study Other
2023-05-27
EGAS00001007295 Exploration of neuroblastoma xenograft models for tumor extracellular RNA profiling in murine blood plasma RNASeq
2023-05-30
EGAS00001007296 Human data for chromatin accessibility (ATAC-Seq and scATAC-Seq) and transcriptome (RNA-Seq and scRNA-Seq) in eight B-cell precursors, from HSC to Naive B cells Other
2023-05-30
EGAS00001007297 Clinical outcomes and immune correlates of response to nivolumab plus chemoradiotherapy in women with locally-advanced cervical cancer – NiCOL study Other
2023-05-30
EGAS00001007298 Early ctDNA molecular response captures therapeutic response in the first stage of CCTG BR.36 ctDNA-directed, multi-center phase II study of molecular response adaptive immunotherapy in non-small cell lung cancer Cancer Genomics
2023-05-30
EGAS00001007299 Circulating tumor DNA, pathological and immunologic responses to neoadjuvant nivolumab or nivolumab plus relatlimab and chemoradiotherapy in resectable esophageal/gastroesophageal junction cancer Cancer Genomics
2023-05-30
EGAS00001007300 RNAseq of Colorectal cancer organoid-stroma biobank cohort Other
2023-05-30
EGAS00001007301 WES of Colorectal cancer organoid-stroma biobank cohort Other
2023-05-30
EGAS00001007302 Baseline RNAseq analysis of POETIC Good/Poor Responders to aromatase inhibitors based on change in Ki67 RNASeq
2023-05-31
EGAS00001007303 Targeted exome DNA sequencing analysis of POETIC Good/Poor Responders to aromatase inhibitors based on change in Ki67 Exome Sequencing
2023-05-31
EGAS00001007305 Healthy human B-lymphopoiesis RNA-Seq reference using FACS sorted bone marrow aspirates RNASeq
2023-05-31
EGAS00001007306 Machine learning guided signal enrichment for ultrasensitive plasma tumor burden monitoring Other
2023-05-31
EGAS00001007307 Human subsistence and signatures of selection on chemosensory genes Population Genomics
2023-06-01
EGAS00001007308 Cell-free DNA sequencing data of healthy control, atrophic gastritis, and gastric cancer patients’ blood Cancer Genomics
2023-06-02
EGAS00001007309 Therapeutic vulnerabilities in CCA from different etiologies identified using integrative multi-omics enhancer activity profiling Epigenetics
2023-06-03
EGAS00001007310 GWAS on covid-19 severity and susceptibility in the province of Bergamo, Italy Other
2023-06-05
EGAS00001007313 ExHiBITT shows that microbiome from colon biopsies, caecal fluid from colonoscopies and faecal samples shape different microbiome-host interactions Other
2023-06-06
EGAS00001007314 Investigation of different library preparation and tissue of origin deconvolution methods for urine and plasma cfDNA methylome analysis Other
2023-06-06
EGAS00001007318 Multiomics analyses of ALS prefrontal cortex tissue Other
2023-06-07
EGAS00001007321 Possible DNA damage after paternal exposure to ionizing radiation in radar technicians Other
2023-06-07
EGAS00001007323 A longitudinal single-cell atlas of treatment response in pediatric AML Other
2023-06-07
EGAS00001007324 Analysis of Loose Ends in Cancer Genome Structure Other
2023-06-07
EGAS00001007327 Pediatric Patient-Derived-Xenograft development in MAPPYACTS – international pediatric cancer precision medicine trial in relapsed and refractory tumors Other
2023-06-08
EGAS00001007330 DECONVOLUTION OF HEMATOPOIETIC STEM/PROGENITOR CELL SIGNALING IN HUMAN AML Other
2023-06-09
EGAS00001007331 H3Africa - Stroke Investigative Research and Education Networks Other
2023-06-09
EGAS00001007332 Bone marrow single cell genomics from blood cancer samples Other
2023-06-09
EGAS00001007333 Detection of somatic mutations of angioimmunoblastic T-cell lymphoma Exome Sequencing
2023-06-11
EGAS00001007334 Facial Skin Biophysical Multi-Parameter and Microbiome-Based Korean Skin Cutoype (KSC) Determination Other
2023-06-12
EGAS00001007335 FGFR-driven urothelial cancer Cancer Genomics
2023-06-12
EGAS00001007336 Breast cancer sequencing data Transcriptome Analysis
2023-06-12
EGAS00001007337 Tonsil Sequencing dataset RNASeq
2023-06-12
EGAS00001007339 Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions Other
2023-06-12
EGAS00001007343 ATAC-Seq of healthy and IBD blood samples Other
2023-06-12
EGAS00001007344 ATAC-Seq of inflamed and non-inflamed biopsies Other
2023-06-12
EGAS00001007345 ATAC-Seq of CD4 T cell subsets Other
2023-06-12
EGAS00001007346 Modulation of the peripheral blood immune cell transcriptome by vitamin D3 supplementation in people with a first demyelinating event: a randomized placebo-controlled trial Other
2023-06-14
EGAS00001007349 Organoid_Derivation_Project___GRCh38___TGS Other
2023-06-16
EGAS00001007350 A circulating biomarker for severity of facioscapulohumeral muscular dystrophy Other
2023-06-19
EGAS00001007351 Assessing mitochondrial bioenergetics in coronary artery disease: A translational left ventricular tissue study in humans (The AMBITION study). Other
2023-06-19
EGAS00001007355 The genomic landscape of GCs Other
2023-06-19
EGAS00001007356 Intercellular nanotube-mediated mitochondrial transfer enhances T-cell metabolic fitness and antitumor efficacy Other
2023-06-19
EGAS00001007358 Selective advantage of mutant stem cells in human clonal hematopoiesis is associated with attenuated response to inflammation and aging Other
2023-06-20
EGAS00001007362 Mapping the epigenomic landscape of human monocytes following innate immune activation reveals context-specific mechanisms driving endotoxin tolerance Other
2023-06-22
EGAS00001007363 Towards standardized whole exome sequencing (WES) for cancer patients: lessons from a multicentric pilot study Other
2023-06-22
EGAS00001007364 WES sequencing of TRACERx NSCLC patient-derived xenograft models Other
2023-06-22
EGAS00001007365 Serial TERT rearrangement breakpoint quantification in circulating tumor DNA enables minimal residual disease monitoring in patients with neuroblastoma Other
2023-06-22
EGAS00001007367 bulk TCR-seq data IMCISION Other
2023-06-23
EGAS00001007368 scRNA-seq and scTCR-seq data IMCISION Other
2023-06-23
EGAS00001007369 Cellular composition of spheres derived from lymph nodes of lung cancer patients Other
2023-06-23
EGAS00001007370 Sclerosing Epithelioid Fibrosarcoma sequencing data Other
2023-06-23
EGAS00001007372 Mechanism of action and resistance to Trastuzumab Deruxtecan in patients with metastatic breast cancer Exome Sequencing
2023-06-24
EGAS00001007373 High-resolution, patient-level dissection of IL-23 blockade in cutaneous psoriasis Other
2023-06-25
EGAS00001007374 Genome-wide DNA methylation sequencing identifies epigenetic perturbations in the upper airways under long-term exposure to moderate levels of ambient air pollution Other
2023-06-26
EGAS00001007375 Analysis of the Elements Involved in the Enrichment of a Panel of Genomic Regions by Nanopore Sequencing Using Adaptive Sampling Other
2023-06-26
EGAS00001007379 Multi-region sequencing of PDAC patients Exome Sequencing
2023-06-26
EGAS00001007380 Separation, characterization, and identification of individuals from multi-person blood mixtures with single cell ATAC-seq Forensic or Paleo-genomics
2023-06-27
EGAS00001007381 SNP array ARID1B patients Other
2023-06-27
EGAS00001007383 Recurrent DNMT3B gene rearrangements are associated with unfavorable outcome in dicentric (9;20)-positive pediatric BCP-ALL Other
2023-06-27
EGAS00001007385 Atypical B cells and impaired SARS-CoV-2 neutralisation following heterologous vaccination in the elderly Other
2023-06-28
EGAS00001007386 AT2 COPD Methylomics Other
2023-06-28
EGAS00001007387 AT2 COPD Transcriptomics Other
2023-06-28
EGAS00001007389 Targeting TRIP13 in Wilms Tumor with Nuclear Export Inhibitors Cancer Genomics
2023-06-28
EGAS00001007390 Single cell landscape of Multicentric Castleman Disease in monozygotic twins Whole Genome Sequencing
2023-06-29
EGAS00001007393 Efficacy of nivolumab in pediatric cancers with high mutation burden and mismatch-repair deficiency Other
2023-06-30
EGAS00001007396 Evaluation of somatic mutations in urine samples as a non-invasive method for the detection and molecular classification of endometrial cancer Other
2023-07-03
EGAS00001007397 scRNAsequencing of in vitro expanded limbal stem cells of aniridia donors Other
2023-07-04
EGAS00001007398 Total RNA sequencing from the TNT trial (NCT00532727) Other
2023-07-04
EGAS00001007399 shallow WGS and deep targeted panel on ctDNA in rhabdomyosarcomas Other
2023-07-04
EGAS00001007400 Genome-wide cell-free DNA biological patterns in patients with cancer Other
2023-07-04
EGAS00001007402 Single-cell multi-omics defines the cell-type-specific impact of splicing aberrations in human hematopoietic clonal outgrowths Cancer Genomics
2023-07-05
EGAS00001007403 checup Other
2023-07-06
EGAS00001007404 Genomic and immune signatures predict clinical outcome in newly diagnosed multiple myeloma treated with immunotherapy regimens Cancer Genomics
2023-07-06
EGAS00001007405 Cohesin Mutations in AML Other
2023-07-06
EGAS00001007409 Diagnosis of multisystem inflammatory syndrome in children by a whole-blood transcriptional signature Other
2023-07-06
EGAS00001007411 Analysis of enhancer-promoter connectivity alterations Other
2023-07-07
EGAS00001007412 Genomic evolution and transcriptional changes in the evolution of prostate cancer into neuroendocrine and ductal carcinoma types Other
2023-07-09
EGAS00001007413 Microbiome confounders and quantitative profiling challenge established microbial targets in colorectal cancer developmental stages Metagenomics
2023-07-10
EGAS00001007421 Prognostic markers of DNA methylation and NGS sequencing in progressive glioblastoma from the EORTC-26101 trial Other
2023-07-13
EGAS00001007426 Translation of non-canonical open reading frames as a cancer cell survival mechanism in childhood medulloblastoma Other
2023-07-13
EGAS00001007427 Single-cell proteogenomics of MDS upon AZA Other
2023-07-13
EGAS00001007428 Genomic evolution and transcriptional changes in the evolution of prostate cancer into neuroendocrine and ductal carcinoma types (RNAseq) Other
2023-07-13
EGAS00001007430 Patient-derived organoids identify tailored therapeutic options and determinants of plasticity in sarcomatoid urothelial bladder cancer Cancer Genomics
2023-07-13
EGAS00001007432 Regenerative effects of MSC treatment on busulfan-induced small intestine damaged organoids. Other
2023-07-14
EGAS00001007436 Finding structural variation and functional consequences from primary acute myeloid leukemia cells with complex karyotype (CK-AML) at the single-cell level Cancer Genomics
2023-07-17
EGAS00001007438 Intra-prostatic tumour evolution, steps in metastatic spread and histogenomic associations revealed by integration of multi-region whole genome sequencing with histopathological features Other
2023-07-17
EGAS00001007445 CUPiD, a cfDNA methylation-based tissue-of-origin classifier for Cancers of Unknown Primary Cancer Genomics
2023-07-17
EGAS00001007446 TallFlow: Lineage tracing of immunophenotypic sub populations in T-cell Acute lymphoblastic leukemia by (sc-)WGS Whole Genome Sequencing
2023-07-18
EGAS00001007449 Methylome study on human spermatogenic cells Epigenetics
2023-07-19
EGAS00001007450 RSV infection of primary bronchial epithelial cells in asthma Other
2023-07-20
EGAS00001007451 Machine Learning Signal Enrichment for Ultrasensitive Plasma Tumor Burden Monitoring Other
2023-07-20
EGAS00001007453 Whole_Genome_Sequencing_OMELib__Cord_blood_ Other
2023-07-21
EGAS00001007454 RNA_Seq_OMELib__Cord_blood_ Other
2023-07-21
EGAS00001007458 Whole Genome sequencing of Angolan and Mozambican individuals Other
2023-07-24
EGAS00001007460 Knoll et al Identification of drug candidates targeting monocyte reprogramming in people living with HIV Transcriptome Analysis
2023-07-25
EGAS00001007461 Knoll et al.: The life-saving benefit of dexamethasone in severe COVID-19 is linked to a reversal of monocyte dysregulation Transcriptome Analysis
2023-07-25
EGAS00001007464 Spatiotemporal evolution and inter-patient heterogeneity in primary and recurrent/metastatic head and neck squamous cell carcinoma Other
2023-07-25
EGAS00001007465 BCL3-rearrangements in B-cell lymphoid neoplasms occur in two breakpoint clusters associated with different diseases Cancer Genomics
2023-07-25
EGAS00001007466 Effective reprogramming of patient-derived M2-polarized glioblastoma-associated microglia/macrophages by treatment with GW2580 Other
2023-07-26
EGAS00001007467 AML FLT3 TCR study Other
2023-07-27
EGAS00001007472 scATAC-seq and combined scRNA-seq of the human first trimester neurodevelopment Epigenetics
2023-08-03
EGAS00001007474 Epithelioid haemangioendothelioma (EHE) case series from the Stafford Fox Rare Cancer Program Other
2023-08-04
EGAS00001007475 Ultra-fast deep-learned pediatric CNS tumor classification. Other
2023-08-04
EGAS00001007477 Genome-wide association study of esophageal squamous cell cancer identifies shared and distinct risk variants in African and Chinese populations Cancer Genomics
2023-08-08
EGAS00001007478 Single cell RNA sequencing of cerebrospinal fluid RNASeq
2023-08-08
EGAS00001007479 DLBCLR Other
2023-08-08
EGAS00001007481 Oncoprint GSCCs Other
2023-08-09
EGAS00001007482 Single-cell profiling of co-cultures of GSCCs and macrophages Other
2023-08-09
EGAS00001007484 Discrepancies in Tumour Mutation Burden (TMB) reporting from sequential Endobronchial ultrasound trans bronchial needle aspiration (EBUS TBNA) samples within single lymph node stations Other
2023-08-10
EGAS00001007486 Subclonal somatic copy number alterations emerge and dominate in recurrent osteosarcoma Other
2023-08-10
EGAS00001007487 Optimizing single-cell transcriptomic discrimination of atopic dermatitis versus psoriasis vulgaris Other
2023-08-10
EGAS00001007488 Single cell transcriptomics of human adrenal gland reveal chromosomal alterations in adrenocortical cells Other
2023-08-11
EGAS00001007493 Methylation-based deconvolution of cell-free DNA Epigenetics
2023-08-14
EGAS00001007499 The genomic echoes of the last Green Sahara on the Fulani and Sahelian people Whole Genome Sequencing
2023-08-16
EGAS00001007501 Clinical and genetic factors associated with tumor response to neoadjuvant (chemo)radiotherapy, survival and recurrence risk in rectal cancer Cancer Genomics
2023-08-17
EGAS00001007505 SECRETO Oral metagenome study Metagenomics
2023-08-18
EGAS00001007507 Whole genome sequencing of 108 epileptic patients from CENet cohort Other
2023-08-18
EGAS00001007508 ExomeSeq Neoantigen Immunogenicity Landscapes Other
2023-08-18
EGAS00001007509 RNASeq Neoantigen Immunogenicity Landscape Other
2023-08-18
EGAS00001007510 Immune landscape of oncohistone-mutant gliomas reveals diverse myeloid populations and tumor-promoting behavior Other
2023-08-18
EGAS00001007511 Shared and distinct features of immune checkpoint therapy-induced myocarditis and myositis Transcriptome Analysis
2023-08-21
EGAS00001007513 Systematic analysis of paralogous regions in 41,755 exomes uncovers clinically relevant variation Other
2023-08-22
EGAS00001007519 AfricanNeo aDNA Study Other
2023-08-22
EGAS00001007521 FFPE WGS for optimizing mutation signature extraction from archival HGSC samples Other
2023-08-22
EGAS00001007525 Integrative genomic analyses of European intrahepatic cholangiocarcinoma: new ROS1 fusion gene and PBX1 as prognostic marker Cancer Genomics
2023-08-24
EGAS00001007527 Evolutionary trajectories of IDH-mutant astrocytoma identify molecular grading markers related to cell cycling Other
2023-08-27
EGAS00001007528 RNA sequencing of control OM cells exposed to traffic-related air pollutants RNASeq
2023-08-28
EGAS00001007529 RAGE engagement by SARS-CoV-2 enables monocyte infection and underlies COVID-19 severity RNASeq
2023-08-28
EGAS00001007530 Mevalonate Metabolism fuels pro-inflammatory function of Vd2 T cells RNASeq
2023-08-28
EGAS00001007532 Peripheral blood DNA methylation of Crohn's disease patients starting treatment with either vedolizumab of ustekinumab Other
2023-08-28
EGAS00001007534 RNA sequencing on intestinal biopsies from inflammatory bowel disease patients treated with vehicle control, MEK inhibitor, or infliximab Other
2023-08-29
EGAS00001007538 The effects of inhaled corticosteroids on healthy airways Metagenomics
2023-08-29
EGAS00001007539 CTD-ILD_BALF_and_blood_scRNA-seq_data Transcriptome Analysis
2023-08-30
EGAS00001007542 Massively parallel functional dissection of schizophrenia associated non-coding genetic variants Other
2023-08-30
EGAS00001007545 Machine learning guided signal enrichment for ultrasensitive plasma tumor burden monitoring Other
2023-08-31
EGAS00001007546 GLASS-NL DNA-Methylation Epigenetics
2023-08-31
EGAS00001007547 Study of PD-1 negative CD8 effector T-cells in advanced HCC with single-cell sequencing Other
2023-08-31
EGAS00001007550 Effects of busulfan, fludarabine and clofarabine treatment on human small intestinal organoids generated from healthy donors Other
2023-09-01
EGAS00001007551 GLASS-NL RNA-sequencing Study RNASeq
2023-09-01
EGAS00001007552 RNA sequencing in primary inflammatory (TPP) macrophages treated with a MEK1/2 inhibitor Other
2023-09-01
EGAS00001007553 RNA sequencing in primary inflammatory (TPP) macrophages following deletion of a disease-associated gene desert at chr21q22, disruption of ETS2, or treatment of ETS2-edited macrophages with a HIF1α stabiliser. Other
2023-09-01
EGAS00001007555 Oxidative phosphorylation is a key ontogenetic feature of monocyte immunometabolism promoting myeloid differentiation after birth Other
2023-09-01
EGAS00001007556 Lower respiratory tract single cell and neutrophil extracellular trap profiling of COVID-19-associated pulmonary aspergillosis Transcriptome Analysis
2023-09-01
EGAS00001007560 Determining genome-wide binding of ETS2 by CUT&RUN in primary human macrophages Epigenetics
2023-09-04
EGAS00001007561 Sequential Antigen-loss and Branching Evolution in Lymphoma after Anti-CD19 and Anti-CD20 Targeted T Cell Engaging Immunotherapy Other
2023-09-04
EGAS00001007562 H3K27ac ChIP-seq in primary inflammatory (TPP) macrophages Other
2023-09-04
EGAS00001007563 Immune and clinicopathological features predict HER2-positive breast cancer prognosis in the neoadjuvant NeoALTTO and CALGB 40601 trials Other
2023-09-06
EGAS00001007565 Complex structural variation patterns in pediatric solid tumors Other
2023-09-07
EGAS00001007571 CS Baby Biome Metagenomics
2023-09-11
EGAS00001007573 Low-coverage whole genome sequencing for a highly selective cohort of severe COVID-19 patients Other
2023-09-11
EGAS00001007574 Idiosyncratic and generic single nuclei and spatial transcriptional patterns in papillary and anaplastic thyroid cancers Other
2023-09-11
EGAS00001007575 Structural and Non-Coding Variants Increase the Diagnostic Yield of Clinical Whole Genome Sequencing for Rare Diseases Whole Genome Sequencing
2023-09-13
EGAS00001007577 CDK4 phosphorylation status and rational use for combining CDK4/6 and BRAF/MEK inhibition in advanced thyroid carcinomas Other
2023-09-14
EGAS00001007578 Peripheral blood DNA methylome in adalimumab-treated patients with rheumatoid arthritis Other
2023-09-17
EGAS00001007580 Korea4K: whole genome sequences of 4,157 Koreans with 107 phenotypes derived from extensive health check-ups Other
2023-09-18
EGAS00001007584 Germline variants in patients diagnosed with both uveal and cutaneous melanoma Other
2023-09-22
EGAS00001007585 Exploring the cell-free total RNA transcriptome in diffuse large B-cell lymphoma and primary mediastinal B-cell lymphoma patients as biomarker source in blood plasma liquid biopsies Other
2023-09-25
EGAS00001007590 SMARCB1 loss activates patient-specific distal oncogenic enhancers in malignant rhabdoid tumors Other
2023-10-02
EGAS00001007593 Low-coverage whole-genome sequencing of cancer and healthy plasma circulating DNA Cancer Genomics
2023-10-03
EGAS00001007600 Haplotyping project Other
2023-10-11
EGAS00001007601 PRADO trial - Personalized response-directed surgery and adjuvant therapy after neoadjuvant ipilimumab plus nivolumab in stage III melanoma Other
2023-10-11
EGAS00001007606 Somatic mutations associate with clonal expansion of CD8+ T cells Transcriptome Analysis
2023-10-12
EGAS00001007611 A clinically applicable connectivity signature for glioblastoma includes the tumor network driver CHI3L1 Other
2023-10-20
EGAS00001007618 RNA sequencing of in vitro generated suppressive myeloid cells using parental and Sialidase expressing A549 cancer cell lines Cancer Genomics
2023-10-25
EGAS00001007626 EBNA2 ChIP-Re-ChIP in primary B-cells infected with EBV virus Gene Regulation Study
2023-10-30
EGAS00001007628 DERMATLAS__Leiomyosarcoma_WES Cancer Genomics
2023-10-31
EGAS00001007629 DERMATLAS__Leiomyoma_WES Cancer Genomics
2023-10-31
EGAS00001007630 DERMATLAS__Leiomyoma_RNAseq Cancer Genomics
2023-10-31
EGAS00001007631 DERMATLAS__Leiomyosarcoma_RNAseq Cancer Genomics
2023-10-31
EGAS00001007635 snRNA-seq analysis in multinucleated myogenic FSHD cells identifies heterogeneous FSHD transcriptome signatures associated with embryonic-like program activation and oxidative stress-induced apoptosis Other
2023-11-03
EGAS00001007650 Early evolutionary branching across spatial domains predisposes to clonal replacement under chemotherapy in neuroblastoma Other
2023-11-21
EGAS00001007658 Buccal Sample Methylation for Breast Cancer Detection Other
2023-12-01
EGAS00001007660 Unraveling mutagenic processes influencing the tumor mutational patterns of individuals with Constitutional Mismatch Repair Deficiency Other
2023-12-05
EGAS00001007661 Targeted and shallow whole genome sequencing identifies therapeutic opportunities in p53abn endometrial cancers Other
2023-12-05
EGAS00001007666 DNA-methylation variability in normal mucosa of patients with adenomatous polyps: a marker of field cancerization Epigenetics
2023-12-08
EGAS00001007686 Identification of the cause of juvenile parkinsonism in a case_SYNJ1 Exome Sequencing
2024-01-17
EGAS00001007703 NOTCH1 fusion genes in pediatric T-cell lymphoblastic lymphoma hallmark a common high-risk subgroup with blood TARC levels as possible biomarker Other
2024-01-31
EGAS00001007705 DERMATLAS__Poroma_WES Other
2024-02-01
EGAS00001007708 Evaluation of EBUS-TBNA Aspirates from Advanced NSCLC for Comprehensive Sequencing Platforms Including Whole Genome Sequencing Other
2024-02-01
EGAS00001007709 A proof-of-concept study of sequential treatment with the HDAC inhibitor vorinostat following BRAF and MEK inhibitors in BRAFV600 mutated melanoma Other
2024-02-02
EGAS00001007710 Nala GSI GSAv3 PGx Study Other
2024-02-05
EGAS00001007711 Karyotype Evolution in Response to Chemoradiotherapy and Upon Recurrence of Esophageal Adenocarcinomas Other
2024-02-05
EGAS00001007712 CD8-targeted IL-2 unleashes tumor-specific immunity in human cancer tissue by reviving the dysfunctional T cell pool RNASeq
2024-02-08
EGAS00001007717 noninvasive lung cancer subtyping Other
2024-02-15
EGAS00001007742 Isoform-level profiling of m6A modifications in human brain Other
2024-03-04
EGAS00001007744 RNA isoform repertoire of neuropsychiatric risk genes in human brain Other
2024-03-04
EGAS00001007745 DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_WES Other
2024-03-07
EGAS00001007746 DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_RNAseq Other
2024-03-07
EGAS00001007753 NEOPREDICT-Lung: Neoadjuvant Immunotherapy for Resectable NSCLC Cancer Genomics
2024-03-19
EGAS00001007764 PREGO reference panel - 3234 individuals from Western France. Individuals' birthplaces are available in epsg.io/2154 (RGF93 v1 / Lambert-93 -- France) coordinates. Other
2024-03-27
EGAS00001007766 Discovery of immunotherapy targets for pediatric solid and brain tumors by exon-level expression Other
2024-03-27
EGAS00001007767 Genomic and transcriptomic landscape of T-cell lymphoblastic lymphoma compared to T-cell acute lymphoblastic leukemia: similar subtypes and different fusions Other
2024-04-02
EGAS00001007773 Repli-seq data for 'Replication timing alterations are associated with mutation acquisition during tumour evolution in breast and lung cancer' Other
2024-04-09
EGAS00001007783 Genome-wide DNA Methylation Analysis Reveals a Unique Methylation Pattern for Pleural Mesothelioma Compared to Healthy Pleura and Other Lung Diseases Epigenetics
2024-04-17
EGAS00001007786 Genomic_Advances_in_Sepsis__GAinS__genotyping Other
2024-04-22
EGAS00001007789 Exome_sequencing_of_UK_Birth_Cohorts___Millennium_Cohort_Study Other
2024-04-25
EGAS00001007803 To_profile_the_landscape_of_sebaceous_tumours___RNA Other
2024-05-13
EGAS00001007816 Genetic Effects on the Skin Methylome in Healthy Older Twins Epigenetics
2024-05-15
EGAS00001007818 This study aims to evaluate the relationship between cardiometabolic risk factors and the most common genetic variation (SNPs) Other
2024-05-16
EGAS00001007819 Benchmarking for alignment and variant calling Other
2024-05-16
EGAS00001007831 Measuring the Efficiency of Purging by Nonrandom Mating in Human Populations Population Genomics
2024-05-29
EGAS00001007832 Whole Genome Sequence and RNASeq Samples for Lung Cancer Other
2024-05-30
EGAS00001007840 Tyrol Lifestyle Atlas: Intermittent Fasting Methylation Data Other
2024-06-13
EGAS00001007844 Array-based methylation analysis of SDHB-deficient pheochromocytoma and paraganglioma Cancer Genomics
2024-06-14
EGAS00001007852 Profiling Chromatin Accessibility in Humans Using Adenine Methylation and Long-Read Sequencing Other
2024-06-19
EGAS00001007854 XClone for analyzing somatic copy number alterations Other
2024-06-25
EGAS00001007855 A GWAS study with the AlpeDPD study cohort Other
2024-07-02
EGAS00001007877 Metabolic profiling of patient-derived organoids reveals nucleotide synthesis as a metabolic vulnerability in malignant rhabdoid tumors Other
2024-07-23
EGAS00001007900 Mutational Mechanisms in Multiply Relapsed Pediatric Acute Lymphoblastic Leukemia Other
2024-08-13
EGAS50000000001 Age-dependent association of clonal hematopoiesis with COVID-19 mortality in patients over 60 years Cancer Genomics
2023-04-25
EGAS50000000003 Test Transcriptome Analysis
2023-09-22
EGAS50000000005 Nurminen et al ("GP2Men") Study Primary and Metastatic Prostate Cancer Whole Genome Sequence Data Whole Genome Sequencing
2023-09-20
EGAS50000000006 Full AfricanNeo ModernDNA Study Population Genomics
2023-09-17
EGAS50000000007 QuantSeq 3'-mRNAseq of pathogen-stimulated PBMCs Transcriptome Analysis
2023-10-01
EGAS50000000008 Breast cancer risk SNPs converge on estrogen receptor binding sites commonly shared between breast tumors to locally alter estrogen signalling output Cancer Genomics
2023-09-12
EGAS50000000009 Evaluation of the ERa binding region activity in breast and endometrial cancer Cancer Genomics
2023-10-02
EGAS50000000010 Comprehensive NGS Profiling to Enable Detection of ALK Gene Rearrangements and MET Amplifications in Non-Small Cell Lung Cancer Cancer Genomics
2023-09-18
EGAS50000000012 Systemic Lupus Erythematosus Serum Stimulation of Human Intestinal Organoids Induces Barrier Leakiness and Changes in Goblet Cell Differentiation Transcriptome Analysis
2023-10-03
EGAS50000000014 Transcriptional Reference Map of Human Natural Killler Cells RNASeq
2023-10-03
EGAS50000000015 Efficacy of two different FGFR-inhibitors in a patient with extrahepatic cholangiocarcinoma harboring an FGFR2 mutation Cancer Genomics
2023-10-04
EGAS50000000016 The genomic basis of childhood T-lineage acute lymphoblastic leukemia Cancer Genomics
2023-09-26
EGAS50000000017 FEGA test Metagenomics
2023-10-16
EGAS50000000018 Identification and targeting of extremely high-risk gamma delta T-ALL in children Cancer Genomics
2023-09-26
EGAS50000000019 BAM files of mapped reads from scDNAsequencing Whole Genome Sequencing
2023-10-06
EGAS50000000020 Single-cell somatic copy number variants in brain using different amplification methods and reference genomes Whole Genome Sequencing
2023-10-13
EGAS50000000021 A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome Cancer Genomics
2023-10-17
EGAS50000000022 BRCA1 secondary splice-site mutations Cancer Genomics
2023-09-26
EGAS50000000023 The chemotherapeutic CX-5461 is extremely mutagenic and may increase cancer risk Whole Genome Sequencing
2023-10-14
EGAS50000000024 A comprehensive genetic map of cytokine responses in Lyme borreliosis Population Genomics
2023-10-16
EGAS50000000025 Whole genome sequencing of Sinonasal hemangiopericytoma and patient derived cell line model Whole Genome Sequencing
2023-10-18
EGAS50000000026 Methylome profiling of Solitary fibrous tumor/Hemangiopericytoma (SFT/HPC) and a patient derived cell-line model Epigenetics
2023-10-18
EGAS50000000027 Evaluating potential drug candidates for the treament of Henamgiopericytoma on patient derived cell line models RNASeq
2023-10-18
EGAS50000000029 Human Brain Small Extracellular Vesicles Contain Selectively-Packaged, Full-Length mRNA RNASeq
2023-09-19
EGAS50000000030 Multiomic spatial landscape of innate immune cells at central nervous system borders Transcriptome Analysis
2023-10-13
EGAS50000000031 Whole-exome sequencing data of ovarian clear cell carcinoma in East Asia Exome Sequencing
2023-09-20
EGAS50000000032 Tumor Evolution Analysis Uncovered Immune-Escape Related Mutations in Relapsed Diffuse Large B-Cell Lymphoma Exome Sequencing
2023-10-11
EGAS50000000033 Papua New Guinean Lowlanders Dataset Whole Genome Sequencing
2023-10-05
EGAS50000000034 single cell transcriptomic analysis of tumor samples collected from 5 patients with EMM RNASeq
2023-10-16
EGAS50000000035 Bulk RNAseq of patient samlpes at the stage of NDMM, RRMM without EMM and EMM RNASeq
2023-10-16
EGAS50000000036 WES data from patient samples at the stage of NDMM and EMM and normal samples Exome Sequencing
2023-10-16
EGAS50000000037 Single-cell profiling reveals mechanisms of response to anti-PD-L1 versus anti-PD-L1 combined with anti-CTLA4 in head and neck squamous cell carcinoma Transcriptome Analysis
2023-09-15
EGAS50000000039 Epigenomic dataset of Human Hepatocellular Carcinoma for EpiHK Epigenetics
2023-10-17
EGAS50000000040 Metabolic and molecular consequences of the TBC1D4 p.Arg684Ter variant in human skeletal muscle RNASeq
2023-10-26
EGAS50000000041 ABCB1 expression in HCC biopsies Transcriptome Analysis
2023-10-30
EGAS50000000042 Transcriptome HCCO Hypoxia and Doxorubicin resistance Transcriptome Analysis
2023-10-30
EGAS50000000043 WES in HCCOs with varying Doxorubicin resistance Exome Sequencing
2023-10-30
EGAS50000000045 SARS-CoV2 mRNA-vaccination-induced Immunological Memory in Human Non-Lymphoid and Lymphoid Tissues RNASeq
2023-10-18
EGAS50000000046 Differential gene expression in the colon mucosa of irritable bowel syndrome patients with diarrhea-predominant symptoms RNASeq
2023-10-18
EGAS50000000047 RNAseq and ATACseq on HGSC lines, pre- and post-treatment with an epigenetic drug Epigenetics
2023-11-07
EGAS50000000048 Whole exome sequencing of pediatric soft tissue sarcoma PDX models Exome Sequencing
2023-11-08
EGAS50000000049 NGS on cardiac samples in Hungarian patients of dilated cardiomyopathy Resequencing
2023-11-07
EGAS50000000051 Dataset of DNA methylation profiles of 189 pediatric central nervous system, soft tissue, and bone tumors Epigenetics
2023-10-30
EGAS50000000052 Multimodal epigenetic sequencing analysis for colon cancer Epigenetics
2023-11-06
EGAS50000000053 Long-read-transcriptome-sequencing of CLL and MDS patients uncovers common molecular effects of SF3B1 mutations Transcriptome Sequencing
2023-11-08
EGAS50000000054 Duplex sequencing Exome Sequencing
2023-10-31
EGAS50000000055 Whole-exome sequencing Exome Sequencing
2023-10-31
EGAS50000000056 Recording physiological history of cells with chemical labeling. Cancer Genomics
2023-11-02
EGAS50000000059 Colon cancer targeted sequencing study contaning WBCs, primary tumor tissue and plasma samples Cancer Genomics
2023-09-18
EGAS50000000060 Cerebrospinal fluid cfDNA sequencing for classification of central nervous system glioma Cancer Genomics
2023-11-16
EGAS50000000061 Identification of germline variants in Medullary thyroid carcinoma (MTC) by whole- exome sequencing Exome Sequencing
2023-10-31
EGAS50000000062 Lipomatous tumors with 12q amplification Cancer Genomics
2023-10-24
EGAS50000000063 Lactate metabolism in cancer stem cell fate regulation Epigenetics
2023-10-20
EGAS50000000064 Idiopathic Collapsing Glomerulopathy in Brazilian patients Exome Sequencing
2023-10-16
EGAS50000000065 MediMer: A versatile do-it-yourself peptide-receptive MHC class I multimer platform for tumor neoantigen-specific T cell detection Cancer Genomics
2023-11-15
EGAS50000000067 Genomic determinants of response and resistance to inotuzumab in B-ALL Cancer Genomics
2023-11-14
EGAS50000000068 Single-Cell RNA-seq of Primary High Grade Serous Carcinoma Transcriptome Sequencing
2023-11-10
EGAS50000000069 Whole genome bisulfite sequencing of prostate cancer samples upon oral pimonidazole administration Epigenetics
2023-10-25
EGAS50000000070 A proteogenomic atlas of the human neural retina RNASeq
2023-10-10
EGAS50000000071 Identification of intronic sequences promoting natural skipping of ABCA4 exon 15 using long-read transcriptomics and midigene assays RNASeq
2023-10-10
EGAS50000000075 Targeted sequencing (paired) of HR genes in primary and metastatic patient-derived xenografts (PDXs) of colorectal cancer (CRC) Exome Sequencing
2023-10-27
EGAS50000000080 CHEK2 molecular manuscript Cancer Genomics
2023-10-11
EGAS50000000081 Tumor mutational landscape in individuals with CMMRD Exome Sequencing
2023-10-11
EGAS50000000082 Correlative Genomic Analysis of Durvalumab plus Pazopanib Combination in Patients with Advanced Soft Tissue Sarcomas Cancer Genomics
2023-10-04
EGAS50000000083 Effects of interferon-gamma treatment on human small intestinal organoids generated from healthy donors RNASeq
2023-10-06
EGAS50000000084 PDX gene expression RNASeq
2023-11-20
EGAS50000000086 Synthetic - FEGA Sweden Heilsa synthetic dataset December 2023 Whole Genome Sequencing
2023-11-22
EGAS50000000087 RNA-Sequencing of cervical cancers RNASeq
2023-11-07
EGAS50000000090 300BCG study: human population variation of trained immunity Epigenetics
2023-10-30
EGAS50000000091 The Genomic Map of Poland in Open Access Whole Genome Sequencing
2023-12-06
EGAS50000000096 The Genomic Map of Poland in Open Access Exome Sequencing
2023-12-12
EGAS50000000097 scRNA-seq of monochorionic dizygotic twin chimera PBMC RNASeq
2023-11-18
EGAS50000000098 LCM-isolated buccal epithelial cell sequencing Whole Genome Sequencing
2023-11-18
EGAS50000000100 Paired primary and recurrent patient GBM sample EZH2 binding profiles Epigenetics
2023-11-16
EGAS50000000101 WNT-dependent interaction between inflammatory fibroblasts and FOLR2+ macrophages promotes fibrosis in chronic kidney disease Transcriptome Analysis
2023-11-10
EGAS50000000102 Tumor reactive γδ T cells contribute to a complete response to PD-1 blockade in a Merkel cell carcinoma patient RNASeq
2023-11-27
EGAS50000000103 AVENIO Expanded ctDNA panel sequence alignments (BAMs) from plasma DNA of lung cancer patients from the OSCILLATE trial Cancer Genomics
2023-10-19
EGAS50000000104 Immunomodulatory effects and improved outcomes with cisplatin- vs carboplatin-based chemotherapy plus atezolizumab in urothelial cancer RNASeq
2023-11-28
EGAS50000000105 Efficacy and safety of entrectinib in patients with ROS1-positive advanced/metastatic non-small cell lung cancer (NSCLC) from the Blood First Assay Screening Trial (BFAST) Cancer Genomics
2023-11-28
EGAS50000000106 Heterogeneity of IKZF1 genomic alterations and risk of relapse in childhood B-cell precursor acute lymphoblastic leukemia Cancer Genomics
2023-12-15
EGAS50000000107 Clones derived from early passage tumoroids of colorectal cancer Whole Genome Sequencing
2023-12-18
EGAS50000000108 Transcriptomic profiles of early and late passage metastatic colorectal cancer (mCRC) tumoroids Transcriptome Sequencing
2023-12-18
EGAS50000000109 Effect of ETS2 modulation on chromatin accessibility and enhancer activity in inflammatory (TPP) macrophages Epigenetics
2023-11-20
EGAS50000000114 Whole genome sequencing to detect spontaneous acquired mutations in mismatch repair-deficient human colon organoids Whole Genome Sequencing
2023-12-22
EGAS50000000122 ctDNA Quantification in Blood Plasma Using Deep Learning Based Fragle Tool Cancer Genomics
2023-10-03
EGAS50000000123 Arcagen – thoracic malignancies Exome Sequencing
2023-10-12
EGAS50000000124 Prognostic whole-genome and transcriptome signatures in colorectal cancers Transcriptome Sequencing
2023-09-19
EGAS50000000126 WES data from tumors and matching controls collected from 11 UTSW translocation renal cell carcinoma (tRCC) patients. Exome Sequencing
2023-12-26
EGAS50000000127 RNA-Seq data from tumor samples collected from 12 UTSW translocation renal cell carcinoma (tRCC) patients. RNASeq
2023-12-30
EGAS50000000128 Pharmacological improvement of CFTR function rescues airway epithelial homeostasis and host defense in cystic fibrosis children RNASeq
2023-09-26
EGAS50000000129 Non-coding mutations drive persistence of a founder pre-leukemic clone which initiates late relapse in T-ALL Cancer Genomics
2023-12-20
EGAS50000000130 Altered enhancer-promoter interaction leads to MNX1 expression in pediatric acute myeloid leukemia with t(7;12)(q36;p13) Cancer Genomics
2023-11-28
EGAS50000000131 Low-coverage whole-sequencing of metastasised colorectal cancer samples treated with bevazicumab Whole Genome Sequencing
2023-11-28
EGAS50000000133 Lifelines NEXT Metagenomics
2023-09-19
EGAS50000000135 Cancer-associated fibroblasts promote drug resistance in ALK-driven lung adenocarcinoma cells by upregulating lipid biosynthesis Cancer Genomics
2023-12-01
EGAS50000000136 Residual ANTXR1+ myofibroblasts after chemotherapy inhibit anti-tumor immunity via YAP1 signaling pathway Transcriptome Sequencing
2023-12-14
EGAS50000000137 Capmatinib shows superior efficacy for MET-fusion driven pediatric high-grade glioma and synergizes with radiotherapy Transcriptome Sequencing
2023-12-19
EGAS50000000138 Immune heterogeneity in small cell lung cancer and vulnerability to immune checkpoint blockade Transcriptome Sequencing
2024-01-05
EGAS50000000139 Progressive multifocal leukoencephalopathy (PML) Transcriptome Sequencing
2023-11-09
EGAS50000000140 Multi-omic characterisation of PBMCs in IBD Transcriptome Sequencing
2023-11-06
EGAS50000000141 Investigating differential diagnostic and prognostic biomarkers in primary cutaneous follicle center lymphoma and follicular lymphoma using low-coverage whole-genome sequencing Whole Genome Sequencing
2023-12-21
EGAS50000000142 Multi-omics characterisation of immune cells in Long Covid Transcriptome Sequencing
2023-11-09
EGAS50000000143 Multi-omics characterisation of the response to stimulation in Long Covid patients Transcriptome Sequencing
2024-01-02
EGAS50000000145 SCANDARE MACARON Transcriptome Analysis
2024-01-11
EGAS50000000146 Small‑scale mutations are infrequent as mechanisms of resistance in post‑PARP inhibitor tumour samples in high grade serous ovarian cancer Cancer Genomics
2023-12-04
EGAS50000000147 Heterogeneity and evolution of DNA mutation rates in microsatellite stable colorectal cancer. Higher mutation rates (MR) in metastatic tumours Exome Sequencing
2024-01-12
EGAS50000000148 Redefined indel taxonomy reveals insights into mutational signatures Whole Genome Sequencing
2023-12-07
EGAS50000000149 The mutational landscape and its longitudinal dynamics in relapsed and refractory Hodgkin lymphoma Exome Sequencing
2023-12-19
EGAS50000000150 RNA-Seq analysis of cocaine use disorder in Brodmann Area 9 RNASeq
2023-10-23
EGAS50000000152 Eribulin efficacy in platinum-resistant and refractory high-grade serous ovarian cancer patient-derived xenograft models Cancer Genomics
2023-12-06
EGAS50000000153 Sample Multiplexing Oligo Comparison RNASeq
2024-01-16
EGAS50000000154 Genome-wide NanoRCS sequencing of cfDNA and ctDNA from liquid biopsies of healthy individuals and cancer patients Cancer Genomics
2024-01-15
EGAS50000000155 Epigenomic atlas of organoid development Epigenetics
2023-11-20
EGAS50000000156 Transcriptome of CD4+ T cells and CD8+ T cells in glioblastoma multiforme RNASeq
2023-12-20
EGAS50000000157 Small RNA sequencing of human oocytes and early embryos RNASeq
2023-12-14
EGAS50000000158 Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder RNASeq
2024-01-09
EGAS50000000159 ScRNA-seq of human kidney immune cells of patients with ANCA-associated glomerulonephritis, Lupus Nephritis against a "healthy" nephrectomy control RNASeq
2023-11-27
EGAS50000000160 Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder RNASeq
2024-01-09
EGAS50000000161 Clonally heritable gene expression imparts a layer of diversity within cell types RNASeq
2024-01-05
EGAS50000000162 Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder Whole Genome Sequencing
2024-01-23
EGAS50000000163 Longitudinal copy number variation analysis from plasma DNA of head and neck cancer patients under re-radiotherapy Cancer Genomics
2024-01-23
EGAS50000000164 Mapping Genotypes to Chromatin Accessibility Profiles in Single Cells Epigenetics
2023-12-13
EGAS50000000165 scRaCH-seq fastq files RNASeq
2024-01-14
EGAS50000000166 Nanopore sequencing enables allelic phasing of FLG loss-of-function variants, intragenic copy number variation and methylation status in atopic dermatitis and ichthyosis vulgaris Whole Genome Sequencing
2024-01-18
EGAS50000000167 Origin of second malignancies in children Whole Genome Sequencing
2024-01-16
EGAS50000000168 Neoadjuvant atezolizumab plus chemotherapy in gastric and gastroesophageal junction adenocarcinoma: the phase 2 PANDA trial RNASeq
2023-12-04
EGAS50000000169 Evolutionary Trajectories of Small Cell Lung Cancer under Therapy Cancer Genomics
2024-01-26
EGAS50000000170 CRCbiome: Gut metagenome of Norwegian screening participants using FIT sampling Metagenomics
2024-01-24
EGAS50000000171 Exome sequencing of patient samples from study Exome Sequencing
2024-01-29
EGAS50000000172 Whole transcriptome seq from patient samples Transcriptome Sequencing
2024-01-29
EGAS50000000173 Single-cell transcriptomic analyses of peripheral blood mononuclear cells, peritoneal fluid, and peritoneal metastases from patients with colorectal cancer RNASeq
2023-11-06
EGAS50000000174 Single-cell RNA-sequencing and cellular indexing of transcriptomes and epitopes of peripheral blood mononuclear cells and peritoneal fluid from patients with achalasia RNASeq
2023-11-13
EGAS50000000176 Induced pluripotent stem cell derived pericytes respond to mediators of proliferation and contractility Transcriptome Sequencing
2024-01-28
EGAS50000000178 Analysis of cell type contributions to cell free DNA in health and disease. Whole Genome Sequencing
2023-10-12
EGAS50000000179 Stability of gut microbiome after COVID-19 vaccination in healthy and immuno-compromised individuals Metagenomics
2024-01-26
EGAS50000000180 The assessment of genetic and immunological backgrounds in advanced NSCLC patients treated with immunotherapy Cancer Genomics
2024-01-29
EGAS50000000181 Single cell transcriptomics in expanded Tregs of APS-1 patients RNASeq
2023-12-05
EGAS50000000183 An isoform quantitative trait locus in SBNO2 links genetic susceptibility to Crohn’s disease with defective antimicrobial activity RNASeq
2024-01-20
EGAS50000000185 Exome sequencing of early and late passage Patient Derived Xenogratf Tumoroids with matched Patient Derived Xenogratfs and matched normal liver Exome Sequencing
2024-01-31
EGAS50000000187 nanoCUSA Whole Genome Sequencing
2023-09-29
EGAS50000000188 Evaluation of the Efficacy and Safety of a Clinical Grade Human Induced Pluripotent Stem Cell-Derived Cardiomyocyte Patch: A Pre-Clinical Study Whole Genome Sequencing
2023-11-17
EGAS50000000189 Evaluation of the Efficacy and Safety of a Clinical Grade Human Induced Pluripotent Stem Cell-Derived Cardiomyocyte Patch: A Pre-Clinical Study Exome Sequencing
2023-11-17
EGAS50000000190 EOSC4Cancer Synthetic Colorectal Cancer Genomic data Synthetic Genomics
2024-02-01
EGAS50000000191 Shallow Whole Genome Sequencing of Patient Derived Xenografts Whole Genome Sequencing
2024-02-08
EGAS50000000196 Long read transcriptome of DM1 patients whole blood RNASeq
2024-01-18
EGAS50000000197 Enhanced resolution profiling in twins reveals differential methylation signatures of Type 2 Diabetes with links to its complications Epigenetics
2024-02-07
EGAS50000000198 Gut 16S rRNA/FINRISK 2002 Metagenomics
2023-12-21
EGAS50000000202 PARK7/DJ-1 deficiency modulates microglial activation in response to LPS-induced inflammation Transcriptome Analysis
2024-02-02
EGAS50000000203 The life-saving benefit of dexamethasone in severe COVID-19 is linked to a reversal of monocyte dysregulation RNASeq
2024-01-11
EGAS50000000204 Localised colon cancer WES study contaning WBCs, tissue and plasma samples at different time points Exome Sequencing
2024-02-16
EGAS50000000205 Colorectal cancer functional annotation - ATAC Cancer Genomics
2023-10-02
EGAS50000000206 Colorectal cancer functional annotation - Micro-C Cancer Genomics
2023-10-02
EGAS50000000207 Colorectal cancer functional annotation - ChIP Epigenetics
2023-09-20
EGAS50000000208 Colorectal cancer functional annotation - RNAseq RNASeq
2023-10-02
EGAS50000000209 A Combined Omics and Tissue Biobank for Paediatric Cancers Cancer Genomics
2023-12-18
EGAS50000000210 NGS-based monitoring of the T cell receptor repertoire in living donor kidney transplant patients undergoing combination cell therapy Transcriptome Sequencing
2024-01-11
EGAS50000000211 Prediction of plasma ctDNA fraction and prognostic implications of liquid biopsy in advanced prostate cancer Cancer Genomics
2024-01-09
EGAS50000000212 Improved detection of colibactin-induced mutations by genotoxic E. coli in organoids and colorectal cancer Whole Genome Sequencing
2024-02-05
EGAS50000000213 T-ALL RNA-Seq raw data files RNASeq
2023-12-13
EGAS50000000214 Clonal Evolution and Blastic Plasmacytoid Dendritic Cell Neoplasm - Two Cases Exome Sequencing
2024-02-27
EGAS50000000215 Liquid biopsy for molecular characterization of diffuse large B-cell lymphoma and early assessment of minimal residual disease Cancer Genomics
2024-01-30
EGAS50000000216 DCLRE1B/Apollo germline mutations associated with renal cell carcinoma Exome Sequencing
2024-02-09
EGAS50000000217 Single-cell atlas of penile cancer reveals TP53 mutations as driver for an aggressive phenotype, irrespective of HPV status, and provides clues for treatment personalization Transcriptome Analysis
2024-02-28
EGAS50000000218 Homopolymer switches mediate adaptive mutability in mismatch repair-deficient colorectal cancer Exome Sequencing
2024-01-18
EGAS50000000219 INVADE cohort Transcriptome Analysis
2024-02-29
EGAS50000000220 Comprehensive spatial landscape and plasticity of immunosuppressive fibroblasts in breast cancer Transcriptome Analysis
2023-12-14
EGAS50000000221 HGG panel sequencing Exome Sequencing
2024-02-22
EGAS50000000222 Oxel Pilot Study Exome Sequencing
2024-02-23
EGAS50000000223 Single-cell transcriptomics of neuroblastoma tumors RNASeq
2024-02-01
EGAS50000000224 Repeated sampling RNASeq
2024-01-04
EGAS50000000225 Transcriptomic characterization of the histopathological growth patterns in breast cancer liver metastases RNASeq
2024-02-21
EGAS50000000226 Combined single-cell transcriptomics and T-cell receptor sequencing reveal heterogeneity of mycosis fungoides between and within patients and identify a CD4+ cytotoxic subtype RNASeq
2024-02-26
EGAS50000000227 Spatially resolved transcriptomics reveals profound subclonal heterogeneity and T cell dysfunction in extramedullary myeloma RNASeq
2024-01-24
EGAS50000000228 A comprehensive proteogenomic pipeline for neoantigen discovery to advance personalized cancer immunotherapy Cancer Genomics
2023-11-13
EGAS50000000229 Transcriptional profiling and clonality analysis of peripheral blood B cells and small intestinal plasma cells in celiac disease RNASeq
2024-02-15
EGAS50000000230 Carboxylesterase 1 mediates a distinctive metabolic profile of dendritic cells to attain an inflammatory phenotype Transcriptome Analysis
2024-03-06
EGAS50000000231 Systematic immune cell dysregulation and molecular subtypes revealed by single cell RNA-seq of subjects with type 1 diabetes RNASeq
2024-01-17
EGAS50000000232 Neversmoker lung adenocarcinoma Whole Genome Sequencing
2024-02-20
EGAS50000000233 Patient-Derived Follicular Lymphoma Spheroids recapitulate lymph node signaling and immune profile, uncovering galectin-9 as a novel immunotherapeutic target RNASeq
2023-09-20
EGAS50000000234 cell-Free DNA Genomic Profiling and its Clinical Implementation in Advanced Prostate Cancer Cancer Genomics
2024-02-23
EGAS50000000236 Panel sequencing of endocrine-resistant breast cancer Cancer Genomics
2024-02-23
EGAS50000000237 Somatic mutations of non-malignant T cells Cancer Genomics
2023-10-16
EGAS50000000238 Genomic profiles associated with response to immunotherapy in adolescent and young adult patients with melanoma Exome Sequencing
2024-03-11
EGAS50000000239 Targeted re-sequencing of multi-region sampled tumors in PDAC Resequencing
2023-09-21
EGAS50000000240 MEMORI WES bams Cancer Genomics
2024-01-11
EGAS50000000241 B Cell Receptor Study From Early Breast Cancer Tumour Samples RNASeq
2024-02-14
EGAS50000000242 3' mRNA- sequencing bams RNASeq
2024-01-11
EGAS50000000243 Whole Genome Sequencing of HER2-Positive Metastatic Extramammary Paget’s Disease: A Case Report Whole Genome Sequencing
2024-03-13
EGAS50000000244 Spatiotemporal immune atlas of the first clinical-grade gene-edited pig-to-human kidney xenotransplant RNASeq
2023-10-11
EGAS50000000245 Sensitive circulating tumor DNA based residual disease detection in epithelial ovarian cancer Cancer Genomics
2024-03-04
EGAS50000000246 RNA sequencing of Non-Small Cell Lung Cancer and adjacent normal tissue RNASeq
2024-03-01
EGAS50000000247 INTEGRATIVE MOLECULAR ANALYSIS OF SKIN TUMORS FROM CYLD CUTANEOUS SYNDROME PATIENTS Cancer Genomics
2024-01-30
EGAS50000000249 Single nuclei RNAseq data from HGSOC primary tumour samples RNASeq
2024-02-13
EGAS50000000251 Anti-TIGIT antibody tiragolumab improves PD-L1 blockade via myeloid and Treg cells RNASeq
2024-02-02
EGAS50000000252 A neoadjuvant, phase II trial demonstrates efficacy and tolerability of Talimogene laherparepvec in cutaneous basal cell carcinoma (NeoBCC trial) Transcriptome Analysis
2024-03-12
EGAS50000000254 Mitochondrial DNA mosaicism in human somatic cells Whole Genome Sequencing
2024-03-08
EGAS50000000256 Perturb-seq on CRC Cancer Genomics
2024-02-21
EGAS50000000257 A fast, affordable and minimally-invasive diagnostic test for Cancer of Unknown Primary (CUP) using DNA methylation profiling Cancer Genomics
2024-03-18
EGAS50000000258 TCRseq Resequencing
2024-03-12
EGAS50000000259 Whole Exome Sequencing Exome Sequencing
2024-03-04
EGAS50000000261 Medulloblastoma WES Exome Sequencing
2024-02-26
EGAS50000000262 Medulloblastoma RNAseq RNASeq
2024-02-26
EGAS50000000263 Peripheral blood DNA methylation and transcriptomics of vedolizumab and ustekinumab treatment response in patients with Crohn's disease Epigenetics
2024-03-17
EGAS50000000264 Etiology of congenital thyroid dysfunction in Down Syndrome: a multi-omics investigation RNASeq
2024-03-13
EGAS50000000265 Anti-tumor and Immune Stimulatory Activity of Iberdomide in Myeloma, Including Patients with Cereblon Dysregulation Cancer Genomics
2024-03-07
EGAS50000000266 Non-invasive prediction of immunotherapy response (NIPIT) project Transcriptome Sequencing
2024-01-31
EGAS50000000267 Circulating RNAs prior to endometrial cancer diagnosis Transcriptome Sequencing
2024-02-26
EGAS50000000268 PRADO trial - Personalized response-directed surgery and adjuvant therapy after neoadjuvant ipilimumab plus nivolumab in stage III melanoma Exome Sequencing
2024-03-14
EGAS50000000269 Single cell and spatial transcriptomics of adult human adrenal glands Transcriptome Analysis
2024-03-19
EGAS50000000270 Whole exome sequencing of preneoplasia lung adenocarcinoma Exome Sequencing
2024-02-21
EGAS50000000271 RNAseq of preneoplasia lung adenocarcinoma RNASeq
2024-02-14
EGAS50000000272 Whole genome sequencing of preneoplasia lung adenocarcinoma Whole Genome Sequencing
2024-02-20
EGAS50000000275 Tumor heterogeneity and immune-evasive microenvironment in T follicular helper cell lymphomas Transcriptome Sequencing
2024-03-21
EGAS50000000276 Mutation detection of T follicular helper cell lymphomas Exome Sequencing
2024-03-24
EGAS50000000277 Combination pembrolizumab and radiotherapy induces systemic anti-tumor immune responses in immunologically-cold non-small cell lung cancer Cancer Genomics
2024-02-28
EGAS50000000278 Human lymphoid-neutrophil/monocyte restriction co-ordinately activates increased proliferation despite parallel heterogeneity in transcriptional changes Transcriptome Analysis
2024-03-07
EGAS50000000279 Clonal heterogeneity leads to secondary resistance in a melanoma patient after adoptive cell therapy with tumor-infiltrating lymphocytes Transcriptome Analysis
2024-03-13
EGAS50000000284 Heterogeneity and evolution of DNA mutation rates in microsatellite-stable colorectal cancer Whole Genome Sequencing
2024-02-08
EGAS50000000286 Comprehensive peripheral blood immunoprofiling reveals five immunotypes with immunotherapy response characteristics in cancer patients RNASeq
2024-03-24
EGAS50000000287 Molecular underpinnings of dedifferentiation and aggressiveness in chromophobe renal cell carcinoma Cancer Genomics
2024-03-26
EGAS50000000288 WGS of cord blood hematopoietic stem and progenitor cells Whole Genome Sequencing
2024-03-28
EGAS50000000289 Whole exome RNA sequencing of FFPE material from 49 pediatric BCP-LBL patients. Transcriptome Analysis
2024-03-05
EGAS50000000290 Whole exome sequencing of FFPE material from 41 pediatric BCP-LBL patients. Exome Sequencing
2024-03-05
EGAS50000000291 Multiregion exome sequencing of ovarian immature teratomas Whole Genome Sequencing
2024-02-20
EGAS50000000292 Multiple Myeloma GWAS Meta-analysis Cancer Genomics
2024-03-27
EGAS50000000293 scRNA-seq of CD4+ T cells from blood and tumor of NSCLC patients RNASeq
2024-03-27
EGAS50000000294 scATAC-seq of CD4+ T cells from blood and tumor of NSCLC patients Epigenetics
2024-03-27
EGAS50000000296 Ancient genomes reveal insights into ritual life at Chichén Itzá Population Genomics
2024-03-08
EGAS50000000297 Homopolymer switches mediate adaptive mutability in mismatch repair-deficient colorectal cancer Cancer Genomics
2024-03-28
EGAS50000000298 A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry RNASeq
2024-04-05
EGAS50000000299 Whole-genome variant calling of individuals from the study of allergic diseases in the Canary Islands Whole Genome Sequencing
2024-02-29
EGAS50000000301 Single nucleus and bulk transcriptomics in prefrontal cortex of individuals with alpha synucleinopathies RNASeq
2024-03-19
EGAS50000000302 Single-cell characterization of human GBM reveals regional differences in tumor-infiltrating leukocyte activation Transcriptome Analysis
2024-04-05
EGAS50000000303 Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease RNASeq
2024-04-09
EGAS50000000305 resistance to FGFR inhibitor in FGR2 cancers from DNA sequencing Exome Sequencing
2023-10-24
EGAS50000000306 resistance to FGFR inhibitor from RNA sequencing RNASeq
2023-10-24
EGAS50000000307 Decoding Human Endogenous Retrovirus Expression in Liver Metastatic Colorectal Cancers: Implications for Diagnosis and Prognosis RNASeq
2024-04-07
EGAS50000000309 Platinum-based chemotherapy induces opposing effects on immunotherapy response-related spatial and stromal biomarkers in the bladder cancer microenvironment RNASeq
2024-04-09
EGAS50000000310 Cell type mapping of inflammatory muscle diseases highlights selective myofiber vulnerability in inclusion body myositis RNASeq
2024-04-10
EGAS50000000311 Bulk RNA-seq of monocytes and in vitro cultured monocyte-derived macrophages of ANCA-associated vasculitis patients with active and stable disease and healthy controls Transcriptome Sequencing
2024-03-31
EGAS50000000312 Primary central nervous system lymphoma (PCNSL) biopsies show heterogeneity in gene expression profiles, genetic subtypes, and in vitro drug sensitivity to kinase inhibitors Exome Sequencing
2024-04-11
EGAS50000000314 Tracing tumor evolution and heterogeneity of pleomorphic carcinoma of the lung Exome Sequencing
2024-02-27
EGAS50000000315 Circulating tumor DNA dynamics reveal KRAS G12C mutation heterogeneity and response to treatment with the KRAS G12C inhibitor divarasib in solid tumors Cancer Genomics
2024-02-26
EGAS50000000318 HiDEF-seq single-molecule sequencing of single-strand mismatches and damage Whole Genome Sequencing
2024-04-05
EGAS50000000319 Regulatory Elements active in Insulinomas Epigenetics
2024-04-17
EGAS50000000320 Transcriptome of insulinomas Transcriptome Sequencing
2024-04-17
EGAS50000000321 Whole Genome Sequencing of Insulinomas Whole Genome Sequencing
2024-04-17
EGAS50000000324 Systematic dissection of tumor-normal single-cell ecosystems across a thousand tumors of 30 cancer types RNASeq
2024-04-08
EGAS50000000325 Impact of allogeneic umbilical-cord derived mesenchymal stromal cells on B-cell scRNAseq in patients with systemic lupus erythematosus Transcriptome Sequencing
2024-04-18
EGAS50000000327 Paired Biopsy Project: West Coast Dream Team Whole Genome Sequencing
2024-03-20
EGAS50000000328 Targeted capture, whole genome sequencing, and RNAseq to identify rearrangements in B-cell lymphomas Cancer Genomics
2024-03-18
EGAS50000000329 The variable genomic landscape during osteosarcoma progression: insights from a longitudinal WGS analysis Whole Genome Sequencing
2024-04-24
EGAS50000000330 Targeted sequencing of genomic regions of interest in depression and obesity Population Genomics
2024-04-29
EGAS50000000331 T cell repertorie analysis fom a Spanish cohort of mild and severe cases of COVID-19 recovered patients Transcriptome Sequencing
2024-02-19
EGAS50000000333 ROBUST (NCT02285062) Cancer Genomics
2024-04-15
EGAS50000000334 Toxigenic Clostridium perfringens isolated from at-risk pediatric inflammatory bowel disease patients Metagenomics
2024-02-08
EGAS50000000336 Comparison between phenotypic-defined stage of blasts and transcriptional profile RNASeq
2024-04-29
EGAS50000000337 RNA-sequencing from duodenal bipsies of Celiac disease patients Transcriptome Sequencing
2024-04-29
EGAS50000000338 RNA sequencing from patient-derived intestinal organoids Transcriptome Sequencing
2024-04-30
EGAS50000000339 Single cell transcriptomic profiles of advanced melanoma patients treated with checkpoint inhibitor immunotherapy RNASeq
2024-04-26
EGAS50000000340 Whole-genome sequencing of primary mediastinal large B-cell lymphoma Whole Genome Sequencing
2023-11-01
EGAS50000000342 A single-cell multi-omic atlas of nodal B-cell non-Hodgkin lymphomas Transcriptome Sequencing
2023-11-10
EGAS50000000343 scMultiomics Transcriptome Analysis
2024-01-30
EGAS50000000344 scRNAseq Transcriptome Analysis
2024-01-30
EGAS50000000346 Multi-omic analysis of SDHB-related PCPG Cancer Genomics
2024-04-23
EGAS50000000347 Orthogonal proteogenomic analysis identifies the druggable PA2G4-MYC axis in 3q26 AML Cancer Genomics
2024-05-09
EGAS50000000348 WGS of primary neuroblastoma data Whole Genome Sequencing
2024-02-26
EGAS50000000349 WGS of ecDNA neuroblastoma cell lines Whole Genome Sequencing
2024-05-13
EGAS50000000350 Single cell chromatin accessibility allows analysis of the transposable element landscape, revealing shared features of immune tissue-residency Epigenetics
2024-05-10
EGAS50000000352 Coloured individuals from South Africa Population Genomics
2024-05-02
EGAS50000000353 ST dataset of subcortical MS RNASeq
2024-04-15
EGAS50000000354 snRNA-seq of subcortical MS RNASeq
2024-04-16
EGAS50000000355 Tumor microenvironment-induced FOXM1 regulates ovarian cancer stemness RNASeq
2024-05-13
EGAS50000000356 Novel immunodeficiency caused by homozygous mutations of SLC19A1 Exome Sequencing
2024-04-23
EGAS50000000357 scRNAseq of acute myeloid leukemia Transcriptome Analysis
2024-05-13
EGAS50000000358 TallFlow - multi-omics Transcriptome Sequencing
2024-03-30
EGAS50000000360 The evolution of ovarian high grade serous carcinoma from STIC lesions Whole Genome Sequencing
2023-12-14
EGAS50000000361 The evolution of ovarian high grade serous carcinoma from STIC lesions Cancer Genomics
2024-04-14
EGAS50000000362 Clinical and molecular features of early onset pancreatic cancer Cancer Genomics
2024-05-22
EGAS50000000365 Single-cell RNA sequencing of human skin tumors (BCC, SCC and Melanoma) Transcriptome Sequencing
2023-11-20
EGAS50000000370 CpG methylation changes associated with hyperglycemia in type 1 diabetes occur at angiogenic glomerular and retinal gene loci. Population Genomics
2024-03-19
EGAS50000000372 Genomic and clinical characterization of a familial GIST kindred intolerant to imatinib Cancer Genomics
2024-04-02
EGAS50000000373 Genomic landscape of metastases from 97 patients with metastatic urothelial carcinoma Cancer Genomics
2024-05-05
EGAS50000000376 cfRRBS data plasma healthy donors Epigenetics
2024-05-30
EGAS50000000377 Diagnosis of pediatric central nervous system tumors using methylation profiling of cfDNA from cerebrospinal fluid Epigenetics
2024-05-06
EGAS50000000378 "BaTwa" populations from Zambia retain ancestry of past hunter-gatherer groups Population Genomics
2024-05-13
EGAS50000000381 Epigenetic landscape reorganization and reactivation of embryonic development genes are associated with malignancy in IDH-mutant astrocytoma RNASeq
2024-03-20
EGAS50000000382 Characterization of the cellular microenvironment in fibrostenotic Crohn’s disease RNASeq
2024-05-09
EGAS50000000384 Metagenomic characterization of tracheal aspirates from non-pulmonary sepsis patients Metagenomics
2024-04-26
EGAS50000000385 TOTHER3 Cancer Genomics
2024-05-06
EGAS50000000386 RNA-sequencing of N-ERD patients with Dupilumab therapy RNASeq
2024-06-06
EGAS50000000390 Resolving complex duplication variants using long read genome sequencing in autism spectrum disorder Whole Genome Sequencing
2023-12-19
EGAS50000000391 "Distinct immunometabolic signatures in circulating immune cells define disease outcome in acute-on-chronic liver failure" Transcriptome Analysis
2024-04-23
EGAS50000000394 Whole Exome Sequencing of Multiple Myeloma Patients Exome Sequencing
2024-06-07
EGAS50000000397 Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility RNASeq
2024-06-11
EGAS50000000402 Whole Transcriptome Profiling of prDLBCL Transcriptome Analysis
2024-06-14
EGAS50000000403 Whole exome sequencing of prDLBCL Exome Sequencing
2024-06-14
EGAS50000000405 Non-KMT2Ar infant Acute Lymphoblastic Leukemia Sequencing Cancer Genomics
2024-03-08
EGAS50000000406 Colorectal cancer functional annotation - MPRA Cancer Genomics
2024-06-13
EGAS50000000409 Fecal microbiota transplantation - Effect of engraftment on plasma metabolomics and cllinical outcomes Metagenomics
2024-03-15
EGAS50000000411 Single nuclei ATAC-Seq data from the human ganglionic eminences Epigenetics
2024-05-23
EGAS50000000412 Cell-Free DNA Genomic and Fragmentomic Features for Early Outcome Prediction in Diffuse Large B-Cell Lymphoma Whole Genome Sequencing
2024-05-17
EGAS50000000413 ProstOmics: spatial and bulk multi-omics of prostate cancer Transcriptome Sequencing
2024-04-18
EGAS50000000414 Whole-genome sequencing of high-retrotransposition rate tumours Cancer Genomics
2024-06-05
EGAS50000000415 Cardiometabolic effects of Anaerobutyricum soehngenii Metagenomics
2024-06-07
EGAS50000000416 Tumor inflammation and mutational burden are differentially associated with response to nivolumab or nivolumab plus ipilimumab in metastatic colorectal cancer Cancer Genomics
2024-05-24
EGAS50000000417 DNA methylation database for gynecological cancer detection, classification and assay development Epigenetics
2024-06-25
EGAS50000000423 Genome-wide array data from Eivissan and Menorcan Individuals Population Genomics
2024-06-28
EGAS50000000424 Adipose tissue macrophage dysfunction is associated with a breach of vascular integrity in NASH Transcriptome Analysis
2024-06-20
EGAS50000000425 Heterogeneity and evolution of DNA mutation rates in microsatellite-stable colorectal cancer Whole Genome Sequencing
2024-06-27
EGAS50000000426 Prediction of homologous recombination deficiency identifies colorectal tumors sensitive to PARP inhibition Whole Genome Sequencing
2024-07-02
EGAS50000000427 Cergentis FFPE-TLC Resequencing
2024-06-07
EGAS50000000428 Whole Exome Sequences from Eivissan and Menorcan Individuals Population Genomics
2024-06-21
EGAS50000000429 Whole-exome sequencing of acute myeloid leukemias with aberrations of chromosome 7 Exome Sequencing
2024-07-06
EGAS50000000430 WES analysis of tumor samples Exome Sequencing
2024-07-04
EGAS50000000432 Single-cell RNA sequencing of pediatric Hodgkin Lymphoma to study the inhibition of T cell subtypes RNASeq
2024-07-03
EGAS50000000434 Highly similar genomic landscapes in monoclonal B-cell lymphocytosis and ultra-stable chronic lymphocytic leukemia with low frequency of driver mutations Whole Genome Sequencing
2024-03-27
EGAS50000000435 Identifying New Genetic Subtypes in Follicular Lymphoma Cancer Genomics
2024-05-14
EGAS50000000436 Mind the gap: the relevance of the genome reference to resolve rare and pathogenic inversions Whole Genome Sequencing
2024-06-12
EGAS50000000440 Nanopore sequencing of blood, saliva, buccal mucosa samples of patients with inherited retinal disorders Epigenetics
2024-07-03
EGAS50000000442 Diagnostic yield and clinical utility of whole-exome sequencing in pediatric patients with rare and undiagnosed diseases in the Czech Republic Exome Sequencing
2024-07-10
EGAS50000000443 Duplex sequencing Exome Sequencing
2024-07-15
EGAS50000000444 A 3D genome atlas of breast cancer progression (BRCA3D) Cancer Genomics
2024-07-15
EGAS50000000446 plasma DNA LINE-1 targeted bisulfite sequencing: a new non-invasive multi-cancer detection marker Epigenetics
2024-07-10
EGAS50000000448 RNA Sequencing of AD OM cells exposed to traffic-related air pollutants Transcriptome Analysis
2024-06-14
EGAS50000000449 Personalized peptide vaccination among 173 patients with IDH wildtype glioblastoma: a retrospective analysis Cancer Genomics
2024-06-28
EGAS50000000450 cfDNA Methylomes for HCC Detection and Postoperative Monitoring Epigenetics
2024-05-30
EGAS50000000452 Genome and transcriptome sequencing of cancer of unknown primary tumours Cancer Genomics
2024-05-01
EGAS50000000457 ATAC sequencing of Treg cell subsets Epigenetics
2024-07-10
EGAS50000000458 RNA sequencing of circulating human immune cells before and after interleukin-2 immunotherapy in systemic lupus erythematosus patients RNASeq
2024-07-19
EGAS50000000460 Mosaic structural variation sample Whole Genome Sequencing
2024-06-17
EGAS50000000468 A first step towards clinical routine long-read sequencing in Sweden, a national pilot study on chromosomal rearrangements Whole Genome Sequencing
2024-07-01
EGAS50000000470 Integrating molecular imaging and transcriptomic profiling in advanced HER2-positive breast cancer receiving trastuzumab emtansine (T-DM1): an analysis of the ZEPHIR clinical trial Transcriptome Analysis
2024-06-13
EGAS50000000471 Plasma mutation profile of precursor lesions and colorectal cancer using the Oncomine Colon cfDNA Assay Cancer Genomics
2024-07-25
EGAS50000000473 RNA-Seq of human longitudinal whole blood samples from PCR-positive and PCR-negative recent household contacts of COVID-19 index cases. RNASeq
2024-07-02
EGAS50000000475 Spatial transcriptomics analysis of triple negative breast cancers Transcriptome Analysis
2024-07-16
EGAS50000000476 USH genes sequencing Whole Genome Sequencing
2024-07-16
EGAS50000000478 Ballett Cancer Genomics
2024-07-05
EGAS50000000480 snRNA and snATAC analysis of cocaine use disorder in human caudate nucleus Gene Regulation Study
2024-07-29
EGAS50000000481 Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions Gene Regulation Study
2024-07-29
EGAS50000000483 Neoadjuvant immune checkpoint blockade in women with mismatch repair deficient endometrial cancer Cancer Genomics
2024-08-01
EGAS50000000484 Early detection of ovarian cancer using cell-free DNA fragmentomes and protein biomarkers Cancer Genomics
2024-06-24
EGAS50000000485 A Genomics-Driven Artificial Intelligence-Based Model Classifies Breast Invasive Lobular Carcinoma and Discovers CDH1 Inactivating Mechanisms Whole Genome Sequencing
2024-06-24
EGAS50000000486 resistance mechanims to targeted therapies from DNA sequencing Exome Sequencing
2024-07-29
EGAS50000000487 resistance mechanims to targeted therapies from RNA sequencing RNASeq
2024-07-29
EGAS50000000488 Disease recurrence after pathologic response (Recurrence DNAseq) Exome Sequencing
2024-07-08
EGAS50000000489 Transcriptomic changes in placenta associated with anesthesia, delivery mode and maternal diabetes Transcriptome Analysis
2024-04-18
EGAS50000000490 Ischemia Reperfusion Responses in Human Lung Transplants at the Single Cell Resolution Transcriptome Sequencing
2024-06-26
EGAS50000000492 Immune signature of maligant melanoma in pregnancy RNASeq
2024-08-05
EGAS50000000493 Mate-pair sequencing of 12q-amplified osteosarcomas Whole Genome Sequencing
2024-06-24
EGAS50000000494 RNAseq of 12q-amplified osteosarcomas RNASeq
2024-06-24
EGAS50000000495 Longread sequencing of selected 12q-amplified osteosarcomas Whole Genome Sequencing
2024-06-24
EGAS50000000496 Mid-pass Whole-genome Sequencing in a Malagasy Cohort Uncovers Body Composition Associations Whole Genome Sequencing
2024-07-19
EGAS50000000501 Spatially resolved niche and tumor microenvironmental alterations in gastric cancer peritoneal metastases Cancer Genomics
2024-07-31
EGAS50000000504 The landscape of Usher syndrome-associated transcript isoforms in the human neural retina RNASeq
2024-06-12
EGAS50000000506 SCLC MeDIP Epigenetics
2024-08-08
EGAS50000000508 Sex Differences in MAGEL2 Gene Promoter Methylation in High Functioning Autism - Trends from a Pilot Study Using Nanopore Cas9 Targeted Long Read Sequencing Epigenetics
2024-08-13
EGAS50000000509 ecDNA copy number heterogeneity Cancer Genomics
2024-08-09
EGAS50000000520 Full characterization of structural variation Whole Genome Sequencing
2024-08-14
EGAS50000000522 Target sequencing for 53 synovial sarcoma patients Resequencing
2024-08-13
EGAS50000000525 Identification of HER2-positive breast cancer molecular subtypes with potential clinical implications in the ALTTO clinical trial Transcriptome Analysis
2024-07-24
EGAS50000000528 Single-cell RNA-seq and TCR-seq of synovial tissue and peripheral blood CD4+ and CD8+ T cells from patients with immune-mediated refractory arthritis Transcriptome Sequencing
2023-10-09
EGAS50000000530 Contribution of specific cell types to the development of Barrett’s esophagus and carcinoma via germline genetic risk Transcriptome Analysis
2024-04-10
EGAS50000000534 Single-cell transcriptomic data of 9 DHG-H3G34 patient tumors. Transcriptome Sequencing
2024-07-07
EGAS50000000536 Base-excision repair pathway shapes 5-methylcytosine deamination signatures in pan-cancer genomes Cancer Genomics
2024-07-19
EGAS50000000537 Scywalker: scalable end-to-end data analysis workflow for nanopore single-cell transcriptome sequencing Transcriptome Analysis
2024-06-10
EGAS50000000538 Duplex sequencing of selected breast cancer patients Resequencing
2024-07-18
EGAS50000000539 WES of breast cancer patients and controls Exome Sequencing
2024-07-18
EGAS50000000540 3D genome topology distinguishes molecular subgroups of medulloblastoma Epigenetics
2024-08-19
EGAS50000000552 Nanopore whole genome sequencing data of HG002 Whole Genome Sequencing
2024-08-27
EGAS50000000553 Nanopore whole genome sequencing data of human PGT samples Whole Genome Sequencing
2024-08-27
EGAS50000000558 Characterization of copy number quiet oral cancer Cancer Genomics
2024-08-27
EGAS50000000560 Cancer cell and tumor microenvironment biomarkers associated with disease-free survival with adjuvant nivolumab in the phase 3 CheckMate 274 trial Cancer Genomics
2024-06-03
EGAS50000000561 Divergent WNT Signaling and Drug Sensitivity Profiles within Hepatoblastoma Tumors and Organoids Transcriptome Sequencing
2024-08-21
EGAS50000000565 Whole-Exome Sequencing Plasma Control Samples for Benchmarking Exome Sequencing
2024-09-03
EGAS50000000566 Characterizing the cell-free transcriptome in a humanized DLBCL patient-derived tumor xenograft model for RNA-based liquid biopsy in a preclinical setting RNASeq
2024-08-13
EGAS50000000567 Neoadjuvant nivolumab or nivolumab plus ipilimumab in early-stage triple negative breast cancer: phase 2 adaptive BELLINI trial. RNA-Seq RNASeq
2024-08-15
EGAS50000000568 Neoadjuvant nivolumab or nivolumab plus ipilimumab in early-stage triple negative breast cancer: phase 2 adaptive BELLINI trial. WES Exome Sequencing
2024-08-15
EGAS50000000569 Whole-genome sequencing of BRCA-mutant breast cancer patient samples from tumour, germline tissue and plasma Whole Genome Sequencing
2024-08-27
EGAS50000000570 Repeat expansions with small TTTCA insertions in MARCHF6 cause Familial Adult Myoclonus without Epilepsy Gene Regulation Study
2024-08-22
JGAS000001 Identification and Characterization of Cancer Mutations in Japanese LungAdenocarcinoma without Sequencing of Normal Tissue Counterparts Exome Sequencing
2014-07-17
JGAS000002 Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing. Whole Genome Sequencing
2014-09-03
JGAS000004 Genomic and Genetic Analysis of Brain Tumors and Analysis of Their Clinicopathological Significance Tumor vs. Matched-Normal
2014-09-07
JGAS000005 Gene expression of human Th17 cells before and after activation Transcriptome Analysis
2014-09-08
JGAS000006 DNA methylation dynamics during early human development Whole genome bisulfite sequencing
2014-10-28
JGAS000007 Research for genetic causes and mechanisms of Hirschsprung's or Hirschsprung's related diseases Exome Sequencing
2014-10-30
JGAS000008 Research for candidate genes of splenic epidermoid cyst Exome Sequencing
2014-11-03
JGAS000009 Whole exome sequence analysis in multiple system atrophy Case-Control
2014-11-19
JGAS000011 Systematic identification of long non-coding RNAs potentially involved in gastrointestinal carncer Transcriptome Sequencing
2014-12-21
JGAS000012 Genotype data from Nagahama cohort project Cohort
2014-12-23
JGAS000013 Whole exome sequence analysis in sporadic amyotrophic lateral sclerosis Case Set
2015-01-06
JGAS000014 Genetic analysis in monozygotic twins discordant for bipolar disorder Control Set
2015-01-05
JGAS000015 DNA methylation at HBV integrants and flanking host genomes Tumor vs. Matched-Normal
2015-01-14
JGAS000016 Genetic analysis in lifestyle-related disease, arteriosclerotic disease, and aging-related diseases. Case Set
2015-01-22
JGAS000017 Leukemic evolution of donor-derived cells harboring IDH2 and DNMT3A mutations after allogeneic stem cell transplantation Exome Sequencing
2015-02-01
JGAS000018 An imputation reference panel of HLA variants in Japanese Control Set
2015-03-03
JGAS000021 Genomics characterization of primary central nervous system lymphoma Exome Sequencing
2015-03-04
JGAS000022 Integrated copy number and expression analysis identifies profiles of whole-arm chromosomal alterations and subgroups with favorable outcome in ovarian clear cell carcinomas Tumor vs. Matched-Normal
2015-03-17
JGAS000023 Whole-exome sequencing of MDS and related myeloid neoplasms Tumor vs. Matched-Normal
2015-04-14
JGAS000024 Identification of genetic polymorphism on aggressive periodontitis Case Set
2015-03-26
JGAS000026 Epigenome mapping in purified cells of the digestive and urogenital organs: Participation in International Human Epigenome Consortium (IHEC) (WGBS) Control Set
2015-06-01
JGAS000027 Epigenome mapping in purified cells of the digestive and urogenital organs: Participation in International Human Epigenome Consortium (IHEC) (ChIP-seq) Control Set
2015-05-07
JGAS000028 Epigenome mapping in purified cells of the digestive and urogenital organs: Participation in International Human Epigenome Consortium (IHEC) (RNA-Seq) Control Set
2015-04-27
JGAS000032 Effective screening strategy for deafness using a new-genetation sequencing platform: a consecutive analysis Case Set
2015-08-23
JGAS000035 Searching for rare/low frequency variants in rheumatoid arthritis by exome sequencing Exome Sequencing
2015-08-28
JGAS000036 Whole-exome sequencing of pediatric solid tumors Tumor vs. Matched-Normal
2015-09-05
JGAS000037 Development of molecular targeted therapy for small cell lung cancer by comprehensive genome analysis Case Set
2015-09-23
JGAS000038 Parent-of-origin dependent DNA methylation and gene expression in the human placenta Whole Genome Sequencing
2015-10-06
JGAS000039 Analysis of TKI resistant mechanism for gastrointstinal stromal tumor Exome Sequencing
2015-10-19
JGAS000040 Identification of genetic polymorphism on aggressive periodontitis Case Set
2015-10-24
JGAS000041 Genetic analysis in an inherited cardiac arrhythmia Case-Control
2015-10-27
JGAS000042 Constructing database of magnetic resonance imaging of the brain and the ancillary clinical information for multisite collaboration studies: a dataset from normal individuals Case-Control
2015-11-10
JGAS000043 Constructing database of magnetic resonance imaging of the brain and the ancillary clinical information for multisite collaboration studies: a dataset from Schizophrenia individuals Case-Control
2015-11-10
JGAS000044 Constructing database of magnetic resonance imaging of the brain and the ancillary clinical information for multisite collaboration studies: a dataset from Depression individuals Case-Control
2015-11-10
JGAS000045 Constructing database of magnetic resonance imaging of the brain and the ancillary clinical information for multisite collaboration studies: a dataset from Bipolar disorder individuals Case-Control
2015-11-10
JGAS000046 Genome-wide copy number analysis of neuroblastoma SNP array analysis
2015-12-20
JGAS000047 Transcriptome analysis of adolescents and young adults with Acute Lymphoblastic Leukemia Transcriptome Sequencing
2016-01-06
JGAS000051 Japanese Alzheimer's disease neuroimaging initiative Cohort
2016-02-04
JGAS000052 Research of factors related to diagnosis, progression, prognosis and treatment of hepato-biliary-pancreatic malignancies Tumor vs. Matched-Normal
2016-02-23
JGAS000053 Transcriptome analysis of Hepatitis B for drug discovery and clinical applications Transcriptome Sequencing
2016-03-06
JGAS000057 Homozygous inactivation of CHEK2 is linked to a familial case of multiple primary lung cancer with accompanying cancers in other organs Case Set
2016-05-25
JGAS000059 Genetic and epigentic analysis of non-alcoholic fatty liver disease. Methylation analysis of nonalcoholic fatty liver. Control Set
2016-06-22
JGAS000060 Investigating genomic intratumor heterogeneity in colorectal carcinoma Case-Control
2016-07-07
JGAS000061 Geriatric Oncology Database of genotypes and methylation, gene expression, clinical data, and survey results on psychosocial and physical conditions in Japanese elderly cancer patients to establish truly effective treatment strategy Case Set
2016-07-11
JGAS000062 Identification of new molecular targets with profiling of malignant mesothelioma Exome Sequencing
2016-07-08
JGAS000064 RNA expression profiling of neuromuscular diseases and viral diseases Transcriptome Sequencing
2016-08-15
JGAS000065 Sequencing cancer mutations in various types of lung cancer using the long-read, portable sequencer Case Set
2016-08-15
JGAS000068 RNA-sequence analysis in patients with inclusion body myositis Case Set
2016-08-31
JGAS000070 CAGE analysis for non-small cell lung carcinoma Transcriptome Sequencing
2016-09-20
JGAS000073 Epigenomic analysis of the human placenta and endometrium constituting the fetal-maternal interface Transcriptome Sequencing
2016-10-03
JGAS000075 Intractable Cancer Therapy Development through a New Target Identification by Molecular Profiling Tumor vs. Matched-Normal
2016-10-14
JGAS000076 Project for Development of Innovative Research on Cancer Therapeutics; Identifiying the predictive factors for response to chemoherapy in ovarian cancer Tumor vs. Matched-Normal
2016-10-18
JGAS000077 RNA-seq analysis of BMP-stimulated glioma initiating cells Transcriptome Sequencing
2016-10-27
JGAS000078 Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [BS-Seq ] Control Set
2016-11-13
JGAS000079 Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [ ChIP-Seq ] Control Set
2016-11-13
JGAS000080 Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [RNA-Seq ] Control Set
2016-11-13
JGAS000081 Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [RNA-Seq ] Control Set
2016-12-05
JGAS000082 Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [BS-Seq ] Control Set
2016-12-05
JGAS000085 Expression quantitative trait loci analysis using human immune cells in a Japanese population Expression quantitative trait loci analysis
2017-02-05
JGAS000086 Identification of genetic mutations characteristic for recurrence and metastasis of gastric cancer. Tumor vs. Matched-Normal
2016-12-30
JGAS000087 Identification of genetic mutations characteristic for recurrence and metastasis of lymphoma. Tumor vs. Matched-Normal
2017-01-08
JGAS000088 Genome-wide integrative analysis of pediatric pancreatoblastoma Exome Sequencing
2017-02-28
JGAS000089 Project for Development of Innovative Research on Cancer Therapeutics;Shuttle system between petient-derived xenograft and ex vivo culture for innovative platform of evaluating drug sensitivity. Tumor vs. Matched-Normal
2017-01-10
JGAS000090 Whole transcriptome sequencing of pediatric T-cell acute lymphoblastic leukemia Transcriptome Sequencing
2017-01-18
JGAS000091 Identification of genetic mutations characteristic for recurrence and metastasis of colon and rectal cancer. Tumor vs. Matched-Normal
2016-12-21
JGAS000092 intratumor heterogeneity in colorectal adenoma and carcinoma Tumor vs. Matched-Normal
2017-02-06
JGAS000093 POU4F3 mutation screening in Japanese hearing loss patients. Case Set
2017-03-16
JGAS000094 The elucidation of molecular mechanisms of hematopoietic stem cells focusing on paroxysmal nocturnal hemoglobinuria (PNH)-type cells Tumor vs. Matched-Normal
2017-02-21
JGAS000095 High-coverage whole-genome sequencing reveals structural variations in triple-negative breast cancer Whole Genome Sequencing
2017-03-09
JGAS000096 WGS analysis of a glioma initiating cell line Whole Genome Sequencing
2017-03-10
JGAS000098 Targeted exome sequencing identify compound heterozygous TYK2 mutations in patients with primary immunodeficiency who developed EBV-associated lymphoma Family
2017-04-03
JGAS000099 mutation analysys of Gorlin syndrome Exome Sequencing
2017-04-17
JGAS000101 GWAS for atrial fibrillation in the Japanese population Case-Control
2017-04-18
JGAS000103 Global Architecture of anti-Tumor B-Cell Immunity against Gastric Cancer Transcriptome sequencing (Tumor only)
2017-05-24
JGAS000104 Identification of genetic mutations characteristic for recurrence of serous ovarian cancer. Tumor vs. Matched-Normal
2017-04-14
JGAS000105 High-coverage whole exome sequence in non-TRU-type lung adenocarcinomas Exome Sequencing
2017-05-31
JGAS000106 Molecular analysis of diffuse cerebellar gliomas Tumor vs. Matched-Normal
2017-06-04
JGAS000107 Epigenomic analysis of the human placenta and endometrium constituting the fetal-maternal interface Transcriptome Sequencing
2017-06-04
JGAS000108 Genomic DNA analysis for malignant mesothelioma from the patients of Japan and USA. Tumor vs. Matched-Normal
2017-06-04
JGAS000109 Genome sequencing of biliary tract cancers Whole Genome Sequencing
2017-05-23
JGAS000111 Searching for DNA methylation sites associated with panic disorder Case-Control
2017-06-22
JGAS000112 Epigenome analysis of human trophoblast stem cells Transcriptome Sequencing
2017-06-28
JGAS000113 Comprehensive genomic analysis of colorectal cancer with microsatellite instability Exome Sequencing
2017-07-02
JGAS000114 Biobank Japan genotype and phenotype data GWAS
2017-07-27
JGAS000115 BHD-associated kidney cancer Tumor vs. Matched-Normal
2017-08-29
JGAS000119 Identification of RNA biomarkers in Parkinson's disease patients Case-Control
2017-09-26
JGAS000120 419 Japanese healthy control Control Set
2017-10-01
JGAS000121 Controlling cell differentiation with precision through understanding the structure and dynamics of gene regulatory networks transcriptome, microarray
2017-10-02
JGAS000122 Development of humanized mice for human hematopoisis and immunity research Exome Sequencing
2017-10-16
JGAS000123 WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis Case Set
2017-12-03
JGAS000124 CAGE analysis for endometrial carcinoma Transcriptome Sequencing
2017-12-04
JGAS000125 Neuron-specifc methylome analysis of Alzheimer's disease brain Methylome analysis
2017-12-06
JGAS000126 Genome-wide analysis for non alcoholic fatty liver disease Case-Control
2018-02-06
JGAS000127 Innate myeloid cell sbuset-specific gene expression patterns in the human colon are altered in Crohn's disease patients Transcriptome Sequencing
2018-03-01
JGAS000128 Comprehensive gene analysis of colorectal cancer cases Exome Sequencing
2018-03-18
JGAS000129 Identification of the genes associated with EGFR-mutant lung cancer Case Set
2018-03-20
JGAS000130 Molecular Profiling and Sequential Somatic Mutation Shift in Hypermutator Tumors Harboring POLE Mutations Tumor vs. Matched-Normal
2018-03-28
JGAS000131 Chromatin remodeler CHD7 regulates the stem cell identity of human neural progenitors ChIP Sequencing
2018-04-03
JGAS000132 Transcriptome analysis of Williams syndrome Case-Control
2018-04-05
JGAS000134 Clonal structure and oncogenic potential of liver cirrhosis tissues. Tumor vs. Matched-Normal
2018-05-10
JGAS000135 Treg cell subset-specific gene expression patterns in human head and neck cancer Transcriptome Sequencing
2018-05-22
JGAS000136 Research for drug discovery and elucidation of pathophysiology using disease-specific iPS cells Exome Sequencing
2018-05-29
JGAS000137 Whole genome sequencing and mutation rate analysis of Vietnamese trios with paternal dioxin exposure Whole Genome Sequencing
2018-05-29
JGAS000138 DNA methylation array analysis of pediatric T-cell acute lymphoblastic leukemia DNA methylation array
2018-06-05
JGAS000139 Development of the prevention and therapy of CRC using patient derived culture tissues. Case-Control
2018-06-13
JGAS000140 Target sequencing of 11 hereditary breast cancer genes in Japanese Case-Control
2018-06-06
JGAS000141 Global Architecture of anti-Tumor B-Cell Immunity against Gastric Cancer Transcriptome sequencing (Tumor only)
2018-07-02
JGAS000142 Identification of RNA biomarkers in Parkinson's disease iPSC-derived neuronal cells Case-Control
2018-07-04
JGAS000144 A multicenter study of susceptibility genes to type 1 diabetes Case-Control
2018-07-17
JGAS000145 Na?ve Treg-specific genomic DNA hypomethylation for autoimmune disease susceptibility Whole Genome Sequencing
2018-08-01
JGAS000146 DNA demethylation is associated with malignant progression of low-grade gliomas Tumor vs. Matched-Normal
2018-08-06
JGAS000147 Transcriptome sequencing, DNA methylation analysis, and SNP array analysis of acute lymphoblastic leukemia in Down syndrome Transcriptome Sequencing
2018-08-21
JGAS000149 The exploratory research of diagnositic biomarker and therapeutic targets of renal cell carcinoma. Transcriptome Sequencing
2018-09-12
JGAS000150 Genetic and transcriptional landscape of plasma cells in POEMS syndrome Transcriptome Sequencing
2018-09-15
JGAS000151 WGS analysis of Japanese liver cancer Tumor vs. Matched-Normal
2018-06-18
JGAS000153 Gene expression analysis for nasal polyps Transcriptome Sequencing
2018-10-17
JGAS000155 Whole genome sequencing analysis of esophageal squamous cell carcinoma Tumor vs. Matched-Normal
2018-10-25
JGAS000156 Whole genome sequencing analysis of hepatoblastoma Tumor vs. Matched-Normal
2018-10-26
JGAS000157 Whole genome sequencing analysis of colorectal cancers Tumor vs. Matched-Normal
2018-10-23
JGAS000158 Prediction of response to preoperative chemoradiotherapy in rectal cancer based on whole-exome sequencing and transcriptomic analysis Tumor vs. Matched-Normal
2018-10-29
JGAS000159 3.5KJPNv2, an allele frequency panel of 3,552 Japanese individuals Cohort
2018-12-04
JGAS000160 Susceptibility loci for tanning ability in Japanese population identified by genome-wide association study GWAS
2018-12-05
JGAS000162 Whole exome sequencing of familial MDS, Two patients Exome Sequencing
2018-12-17
JGAS000164 Comprehensive assay for the molecular profiling of cancer by target enrichment from formalin-fixed paraffin-embedded specimens Target sequencing
2019-02-04
JGAS000165 Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [ ChIP-Seq ] Control Set
2019-02-13
JGAS000166 OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients. Case Set
2019-03-26
JGAS000169 Whole exome sequencing of uterine adenomyosis Exome Sequencing
2019-03-25
JGAS000170 Transcriptome analysis of Familial dysautonomia patient cells treated with splice-regulating compounds Transcriptome Sequencing
2019-04-07
JGAS000171 C-MACH reduced-representation bisulfite sequencing (RRBS) RRBS
2019-04-04
JGAS000172 Comprehensive sequencing analyses of uterine and ovarian carcinosarcoma Tumor vs. Matched-Normal
2019-04-09
JGAS000173 Building a Database of Genomic Structural Variants in Japanese population Control Set
2019-04-17
JGAS000174 Development of actionable molecular targets and/or biomarkers for prognostication and patient stratification in gynecological cancer based on whole-exome sequencing and epigenomic analysis Tumor vs. Matched-Normal
2019-04-21
JGAS000176 Genomic Structural Variants in Japanese Malignant mesothelioma patients Case Set
2019-04-27
JGAS000177 Integrated Exome and RNA Sequencing of Dedifferentiated Liposarcoma Tumor vs. Matched-Normal
2019-05-09
JGAS000178 Comprehensive genomic analysis of patient derived orthotopic xenograft model in primary central nervous system lymphoma Exome Sequencing
2019-05-17
JGAS000179 Identification of driver oncogenes in scirrhous-type gastric cancer cell lines Exome Sequencing
2019-05-22
JGAS000180 Nanopore whole-genome sequencing of sample RK067 and variant-call data (SNVs and intermediate-sized deletions) of 174 Japanese samples. Whole Genome Sequencing
2019-05-28
JGAS000182 Analysis of genomic alterations in dedifferentiated liposarcoma Tumor vs. Matched-Normal
2019-06-09
JGAS000186 Shotgun metagenome sequencing of saliva samples using PromethION Control Set
2019-06-20
JGAS000188 Integrated multi-omics analysis of pediatric hepatoblastoma Transcriptome Sequencing
2019-06-26
JGAS000189 Target sequencing of ROS1-rearranged lung cancer patients Target capture sequencing
2019-07-10
JGAS000190 Whole-genome sequencing on hepatocellular carcinoma with nodule-in-nodule appearance reveals stepwise cancer evolution Whole Genome Sequencing
2019-07-12
JGAS000191 CLDN14 mutation identifed from Japanese sensorineural hearing loss patient. Case Set
2019-07-21
JGAS000192 Mutational Spectrums and Clinical Features of Patients with LOXHD1 Variants Identified in a 8,074 Hearing Loss Patient Cohort. Case Set
2019-07-22
JGAS000194 Viral integration analysis of hepatocellular carcinoma using virus capture sequence. Virus Capture Sequencing
2019-07-23
JGAS000196 Targeted sequencing of cell free DNA samples from oligometastatic colorectal cancer patients Case Set
2019-08-05
JGAS000197 Whole-genome bisulfite sequencing for high-grade glioma Whole-genome bisulfite sequencing
2019-07-07
JGAS000198 Identification of therapeutic target molecules for prostate cancer by using next generation sequencer Transcriptome Sequencing
2019-08-26
JGAS000199 Somatic inflammatory gene mutations accumulate in human ulcerative colitis epithelium Exome Sequencing
2019-08-29
JGAS000200 Mid-frequency hearing loss is a characteristic clinical feature of OTOA-associated hearing loss Case Set
2019-09-01
JGAS000201 The prevalence and clinical characteristics of TECTA-associated autosomal dominant hearing loss. Case Set
2019-09-01
JGAS000202 Genomic Profiling Reveals Heterogeneous Populations of Ductal Carcinoma In Situ Tumor vs. Matched-Normal
2019-09-09
JGAS000203 Target sequencing of 8 hereditary prostate cancer genes in Japanese Case-Control
2019-09-04
JGAS000204 Comprehensive genetic analysis of pediatric germ cell tumors Transcriptome Sequencing
2019-10-02
JGAS000205 Elucidation of disease state by multi-layered omics analysis Population
2019-10-02
JGAS000206 Establishment of an integrated database for clinical and genomic data in cancer Targeted capture sequence
2019-10-07
JGAS000207 Epigenomic analysis of human androgenetic trophoblast stem cells derived from complete hydatidiform mole Transcriptome Sequencing
2019-10-22
JGAS000211 Elucidation of genomic pathology of a patient with concurrent acute myeloid leukemia and mediastinal germ cell tumor Exome Sequencing
2019-12-17
JGAS000214 comprehensive genetic analysis and database construction for head and neck cancer Exome Sequencing
2020-01-05
JGAS000215 Comprehensive molecular and clinicopathological profiling of lung adenocarcinoma in Japanese never or light smokers Exome Sequencing
2020-01-07
JGAS000216 Whole exome sequencing of surgically resected lung adenocarcinomas and gastric adenocarcinomas. Exome Sequencing
2020-01-20
JGAS000217 Sequence analysis of colorectal serrated lesions Case Set
2020-01-26
JGAS000218 Expression profiling of Gorlin iPSCs in the osteoblast induction culture Case-Control
2020-02-13
JGAS000220 Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases Transcriptome Sequencing
2020-03-23
JGAS000221 The genetic analysis of circulating tumor DNA in blood of the digestive cancer patients to investigate the prognostic factors of metastasis and reccurence. Tumor vs. Matched-Normal
2020-03-25
JGAS000222 Ten colorectal cancer patients with locally advanced primary tumors who underwent primary tumor resection following neoadjuvant chemotherapy (NAC). Tumor vs. Matched-Normal
2020-03-25
JGAS000223 Influence of pre-analytical processing on blood protein profiles (AMED-Metabolites) Quantitative proteomics
2020-03-26
JGAS000224 Identification of responsible genes and development of standardized medicine for familial breast cancer by genetic analysis with NGS technology Tumor vs. Matched-Normal
2020-03-26
JGAS000225 Transcriptome analysis of Fabry disease iPSC-derived cardiomyocytes treated with splice-regulating compound; RECTAS Transcriptome Sequencing
2020-04-02
JGAS000226 Mortality and risk of progression to adult T-cell leukemia/lymphoma in patients with HTLV-1-associated myelopathy/tropical spastic paraparesis Tumor vs. Matched-Normal
2020-04-02
JGAS000227 Whole exome sequencing of patients with esophageal squamous cell carcinoma receiving chemoradiotherapy Tumor vs. Matched-Normal
2020-04-06
JGAS000228 Defined Lifestyle and Germline Factors Predispose Asian Populations to Gastric Cancer Exome Sequencing
2020-04-09
JGAS000229 Defined Lifestyle and Germline Factors Predispose Asian Populations to Gastric Cancer Exome Sequencing
2020-04-12
JGAS000230 Identification and characterization of molecular markers in aging and neuronal disorders Transcriptome Sequencing
2020-04-29
JGAS000231 Analysis of mutational and proteomic heterogeneity of gastric cancer to monitor post-treatment tumor burden using circulating tumor DNA Tumor vs. Matched-Normal
2020-05-26
JGAS000232 The analysis of gene mutations in Hematology malignancy Exome Sequencing
2020-06-10
JGAS000233 Genome and gene analysis of gastrointestinal cancer and elucidation of its clinicopathological significance Exome Sequencing
2020-05-17
JGAS000234 Genomic and transcriptomic analysis on hepatocarcinogenesis after HCV eradication Case-Control
2020-06-15
JGAS000236 Paediatric Hepatic International Tumour Trial (JPLT2: PHITT) Exome Sequencing
2020-06-18
JGAS000237 An Organoid Biobank of Rare Human Neuroendocrine Neoplasms Enables Genotype-Phenotype Mapping Whole Genome Sequencing
2020-06-25
JGAS000238 Demographic History and Local Adaptation in Asian Population Population
2020-07-09
JGAS000239 TMM whole genome analysis of 4566 Japanese individuals Cohort
2020-07-15
JGAS000240 Inherited chromosomally-integrated human herpesvirus 6A/B (HHV-6A/B) genome sequences in the Japanese population Whole Genome Sequencing
2020-07-19
JGAS000241 Genomic profiling identified ERCC2 helicase domain mutations respond to platinum-based neoadjuvant therapy in urothelial bladder cancer Tumor vs. Matched-Normal
2020-07-20
JGAS000242 Immunogenomic analysis of tumor infiltrating B cells in gastric cancer Repertoire sequencing (Tumor vs. Matched-Normal)
2020-07-20
JGAS000243 Frequent post-treatment monitoring of colorectal cancer using individualized ctDNA validated by multi-regional molecular profiling Tumor vs. Matched-Normal
2020-07-27
JGAS000244 Whole exome sequencing of solid tumors which received PD-1 blockade therapy Exome Sequencing
2020-07-28
JGAS000245 Identifying aberrant splicing isoforms and potential neoantigens in non-small cell lung cancer Tumor vs. Matched-Normal
2020-07-27
JGAS000246 Multi-omics analysis of pediatric high-risk neuroblastoma Transcriptome Sequencing
2020-07-30
JGAS000248 CAGE-seq analysis of osteoblast derived from cleidocranial dysplasia human induced pluripotent stem cells Transcriptome Sequencing
2020-08-27
JGAS000249 Pilot study of adoptive cell therapy using cultured tumor infiltrating lymphocytes for Japanese melanoma patients refractory to immune-checkpoint inhibitors Exome Sequencing
2020-09-07
JGAS000253 Development of hunanized mice for human hematopoisis and immunity research Transcriptome Sequencing
2020-09-18
JGAS000256 Gene expression data of 2D duodenum organoids with or without continuous flow RNA Sequencing
2020-10-11
JGAS000257 Cell-free DNA sequencing using newly developed single-strand DNA library preparation Whole Genome Sequencing
2020-10-13
JGAS000258 Whole genome sequence analysis in patients with primary central nervous system lymphomas Exome Sequencing
2020-10-25
JGAS000259 Japanese Reference Genome JG1 Whole Genome Sequencing
2020-11-03
JGAS000260 Elucidation of disease state by multi-layered omics analysis Population
2020-11-23
JGAS000262 Hi-C analysis of patient-derived pancreas neoplasm organoids Hi-C
2020-12-07
JGAS000263 Whole exome sequencing and RNA sequencing of patient-derived pancreas neoplasm organoids Exome Sequencing
2020-12-07
JGAS000264 ATAC-seq and ChIP-seq analysis of patient-derived normal pancreas and pancreas neoplasm organoids ATAC sequencing
2020-12-07
JGAS000265 Long-read methylation analysis of breast cancer using the enzymatic base conversion and the nanopore sequencing Tumor vs. Matched-Normal
2020-12-14
JGAS000267 Identification of biomarkers for prediction of efficacy of microtubule inhibitors and antifolates in non-small cell lung cancer Case Set
2021-01-17
JGAS000269 Comprehensive analyses of genetic aberrations in gastroenterological tumors Exome Sequencing
2021-01-12
JGAS000270 Comprehensive molecular and clinicopathological profiling of desmoid tumors Exome Sequencing
2021-01-21
JGAS000272 Clinical and neuroimaging study on preclinical Alzheimer's disease. Longitudinal
2021-01-17
JGAS000273 Whole exome sequencing of 69 trios with bipolar disorder Exome Sequencing
2021-03-02
JGAS000274 PanCancer genome analysis in 5143 Japanese cancer patients Tumor vs. Matched-Normal
2021-03-03
JGAS000276 Comprehensive genomic analysis for AYA with acute lymphoblastic leukemia Transcriptome Sequencing
2021-03-11
JGAS000277 Brain Mapping by Integrated Neurotechnologies for Disease Studies: Human Brain Aging Imaging Study Clinical Trial
2021-03-09
JGAS000278 Phase II clinical trial of adult Philadelphia chromosome-negative precursor B-cell acute lymphocytic leukemia with combination chemotherapy Transcriptome Sequencing
2021-03-11
JGAS000279 Whole exome sequencing of colorectal cancer Exome Sequencing
2021-03-15
JGAS000280 Proteogenomic discovery of a novel class of cancer antigens by HLA ligandome analysis of colon cancer tissues Transcriptome Sequencing
2021-03-28
JGAS000281 Single B cell analysis in pemphigus patients Transcriptome Sequencing
2021-03-31
JGAS000282 NGS-based targeted exome sequencing of osteosarcoma Tumor vs. Matched-Normal
2021-04-04
JGAS000285 Whole exome sequencing, RNA sequencing and single-cell RNA sequencing of 4 melanoma patients Exome Sequencing
2021-04-19
JGAS000286 Building a Database of Genomic Structural Variants in Japanese population Control Set
2021-03-15
JGAS000288 Total NF1 sequence in the patients with neurofaibromatosis type1 Case Set
2021-05-06
JGAS000289 The single plasma-cell transcriptional landscape in POEMS syndrome Transcriptome Sequencing
2021-04-04
JGAS000290 Efficient prediction of a spatial transcriptomics profile better characterizes breast cancer tissue sections without costly experimentation Case Set
2021-05-06
JGAS000292 Comprehensive analysis of the abnormality of the genes in juvenile myelomonocytic leukemia Methylation analysis
2021-05-16
JGAS000293 Combined landscape of single-nucleotide variants and copy-number alterations in clonal hematopoiesis Population
2021-05-18
JGAS000294 Whole Transcriptome Sequencing of NXF1 or CRM1 depleted Cell Transcriptome Sequencing
2021-05-18
JGAS000295 Sensitive gene analysis of hereditary cardiovascular disease Case Set
2021-05-17
JGAS000296 Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases Transcriptome Sequencing
2021-06-01
JGAS000297 Comprehensive molecular profiling of pulmonary pleomorphic carcinoma Exome Sequencing
2021-06-02
JGAS000300 Phylogenetic analysis of combined lobular and ductal carcinoma of the breast Tumor vs. Matched-Normal
2021-06-06
JGAS000301 Genetic drivers define transcriptomic characteristics and clonal hierarchy within intratumoral heterogeneity in adult T-cell leukemia-lymphoma Tumor vs. Matched-Normal
2021-06-09
JGAS000303 Analysis of genes related to the oncogenesis, progression or effectiveness of drug therapies of urological tumors . Single Cell RNA Sequencing
2021-06-15
JGAS000304 Mutational anysis of breast cancer stem cells Case Set
2021-06-17
JGAS000305 Single cell RNA seq of breast cancer stem cells Population
2021-06-17
JGAS000307 Genetics of diffuse large B-cell lymphoma in Japan targeted DNA sequencing
2021-06-21
JGAS000308 Development of a diagnostic gene panel for Gorlin syndrome and its application to liquid biopsy Gene panel sequencing
2021-06-23
JGAS000309 Single cell transcriptome analysis of breast invasive carcinoma Transcriptome Sequencing
2021-06-27
JGAS000310 Genome sequence comparison of human iPS cell lines Whole Genome Sequencing
2021-07-06
JGAS000311 Elucidation of molecular mechanism of NAFLD-HCC Case-Control
2021-07-06
JGAS000312 CCR8-targeted specific depletion of clonally expanded Treg cells in tumor tissues evokes potent tumor immunity with long-lasting memory Transcriptome Sequencing
2021-07-06
JGAS000313 Whole-exome sequencing of Helicobacter pylori-uninfected normal gastric gland Control Set
2021-07-08
JGAS000314 KIR imputation panel Control Set
2021-07-14
JGAS000316 Elucidation of disease state by multi-layered omics analysis Population
2021-07-29
JGAS000317 Mechanisms on relapse after allogeneic hematopoietic cell transplantation in CMML Transcriptome Sequencing
2021-07-29
JGAS000318 Identification of RNA biomarkers in Parkinson's disease iPSC-derived neuronal cells Case-Control
2021-07-30
JGAS000320 Whole Genome Sequencing Analysis of Adult T-cell Leukemia/Lymphoma Whole Genome Sequencing
2021-08-04
JGAS000321 Comprehensive analysis of interaction between human gene expression and environmental metagenomes. Cohort
2021-08-10
JGAS000323 Prevalence and Clinical Characteristics of hearing loss caused by MYH14 mutation Case Set
2021-08-01
JGAS000325 Targeted sequencing of vascular malformations tissues and paired blood samples Tumor vs. Matched-Normal
2021-08-18
JGAS000327 Target sequencing of 27 cancer-predisposing genes in Japanese pancreatic cancer patients Case-Control
2021-08-26
JGAS000330 Development of blood-based biomarkers for precision medicine in castration-resistant prostate cancer Cohort
2021-09-06
JGAS000335 Exploration of predictive biomarkers for postoperative recurrence of stage II/III colorectal cancer using genomic sequencing Exome Sequencing
2021-09-15
JGAS000341 Response to Hepatitis B vaccine Case-Control
2021-09-26
JGAS000346 Target sequencing of 27 cancer-predisposing genes in Japanese colorectal cancer patients Case-Control
2021-09-05
JGAS000347 Impact of germline pathogenic variants in 27 cancer-predisposing genes on the risk of lymphoma Case-Control
2021-09-05
JGAS000348 Whole-genome analysis of a healthy man with common trichromatic vision Whole Genome Sequencing
2021-09-27
JGAS000349 Analysis of chromosomal background of cancerous mutations using a long-read sequencer Tumor vs. Matched-Normal
2021-09-28
JGAS000350 The characterization of gene expression pattern of anticancer agent-resistant cancer stem cells using RNA sequencing analysis. Transcriptome Sequencing
2021-09-30
JGAS000359 Elucidation of molecular mechanisms of tumorigenesis and development of diagnoses and treatments based on comprehensive genomic analyses in pancreatic tumors, duodenal tumors and biliary tumors Tumor vs. Matched-Normal
2021-10-06
JGAS000360 Different malignant tumor samples including lung cancer, colon cancer and breast cancer. Tumor vs. Matched-Normal
2021-10-07
JGAS000361 Whole genome analysis of liver cancer by long-read sequencing Whole Genome Sequencing
2021-10-10
JGAS000367 Whole exome sequencing and RNA-seq of esophageal squamous cell carcinoma Tumor vs. Matched-Normal
2021-10-17
JGAS000368 Comprehensive molecular profiling for breast cancer patients and high-risk individuals. Target sequencing
2021-10-21
JGAS000370 Discovering novel mechanisms of taxane resistance in human breast cancer by whole-exome sequencing Exome Sequencing
2021-10-25
JGAS000377 Comprehensive molecular profiling of subsequent solid cancers after allogenic hematopoietic cell transplantation Exome Sequencing
2021-11-03
JGAS000378 The RNA, ChIP and whole exome sequencing analysis of human colorectal cancer organoids and normal colon organoids treated with (+)-JQ1 Transcriptome Sequencing
2021-11-03
JGAS000379 Filtered variants including SLC12A2 in patients with hearing loss Parent-Offspring Trios
2021-11-04
JGAS000381 Biobank Japan WGS data of myocardial infarction and dementia Whole Genome Sequencing
2021-11-08
JGAS000382 Transcriptome analysis of iPSC-derived hepatocytes from Wilson's Disease patients and healthy controls Case-Control
2021-10-21
JGAS000383 Analysis of the relationship between disease phenotype and genotype in patients with Alzheimer's disease Case Set
2021-11-18
JGAS000385 Multi-omics characterization of KMT2A-rearranged infant acute lymphoblastic leukemia Transcriptome Sequencing
2021-11-18
JGAS000387 Semibulk RNA-seq analysis as a convenient method for measuring gene expression statuses in a local cellular environment Tumor vs. Matched-Normal
2021-11-23
JGAS000389 Genome sequencing of biliary tract cancers Whole Genome Sequencing
2021-11-24
JGAS000412 Biobank Japan genotype data Biobank
2021-11-23
JGAS000413 Genetic analysis of non-small cell lung cancer patients and PDX tumor harboring driver gene alteration Exome Sequencing
2021-11-30
JGAS000414 Target sequencing of 27 cancer-predisposing genes and 13 renal cell carcinoma-related genes in Japanese renal cell carcinoma patients Case-Control
2021-12-06
JGAS000415 Whole gut virome analysis of 476 Japanese revealed a link between phage and autoimmune disease Population
2021-12-08
JGAS000416 Non-invasive human skin transcriptome analysis using mRNA in skin surface lipids Transcriptome Sequencing
2021-12-12
JGAS000417 Non-invasive human skin transcriptome analysis using mRNA in skin surface lipids Transcriptome Sequencing
2021-12-12
JGAS000418 Non-invasive human skin transcriptome analysis using mRNA in skin surface lipids Transcriptome Sequencing
2021-12-12
JGAS000454 The impact of CCR8+ regulatory T cells on cytotoxic T cell function in human lung cancer Transcriptome Sequencing
2021-12-14
JGAS000480 Single cell sequences in patients with malignant tumors single cell RNA sequence
2021-12-14
JGAS000482 Myasthenia gravis-specific aberrant neuromuscular gene expression by medullary thymic epithelial cells in thymoma Transcriptome Sequencing
2021-12-16
JGAS000483 Target sequencing of refractory adult Ph-negative B-ALL 1 patient Case Set
2021-12-20
JGAS000485 Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases Transcriptome Sequencing
2021-12-21
JGAS000486 Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases Transcriptome Sequencing
2021-12-22
JGAS000487 Common and rare germline variants in Japanese prostate cancer patients Cohort
2021-12-22
JGAS000488 exploration of biomarkers discriminating squamous cell carcinoma from other lung cancers Transcriptome Sequencing
2022-01-10
JGAS000489 exploration of biomarkers in colorectal cancer Transcriptome Sequencing
2022-01-10
JGAS000490 Mutation screening in a large series of Japanese hearing loss patients using massively parallel DNA sequencing analysis. Case Set
2022-01-10
JGAS000504 Genetic architecture of microRNA expression and its link to complex diseases in the Japanese population Population
2022-02-02
JGAS000505 Building a Database of Genomic Structural Variants in Japanese population Control Set
2022-02-02
JGAS000507 Whole exome sequence and transcliptomic analysis of tumor tissues with hepatocellular carcinoma and metastatic liver cancer Exome Sequencing
2022-02-09
JGAS000508 Microarray genotyping of idiopathic hypersomnia patients (11 orexin mutation-positive patients, 85 orexin mutation-negative patients) Case Set
2022-02-18
JGAS000510 A study on personalized medicine in genitourinary cancers using genetic biomarkers Tumor vs. Matched-Normal
2022-03-02
JGAS000514 HNF1B induced three-dimentional genome analysis of patient-derived pancreas neoplasm organoids Transcriptome Sequencing
2022-03-21
JGAS000515 Bisulfite sequencing of cell-free DNA in NMOSD patients Case-Control
2022-03-23
JGAS000516 Comprehansive analysis of somatic mutations and genetic variations with whole genome sequencing RNA-seq
2022-03-27
JGAS000520 An efficient procedure for the recovery of DNA from formalin-fixed paraffin-embedded tissue sections Whole Genome Sequencing
2022-04-13
JGAS000522 Next-generation sequencing-based comprehensive genetic analysis of undiagnosed disease Exome Sequencing
2022-04-18
JGAS000523 Elucidation of molecular mechanism of NAFLD-HCC Tumor vs. Matched-Normal
2022-04-18
JGAS000528 Single cell RNA sequencing of human cord Blood CD34 Cells Mutiomics
2022-05-15
JGAS000529 Molecular profiling for a patient with lipoblastoma-like tumor of the vulva Whole Genome Sequencing
2022-05-15
JGAS000530 Metagenome shotgun sequencing of the Inflammatory Bowel Disease Case-Control
2022-05-18
JGAS000531 Reconstruction of the microbial genomes from the Japanese gut metagenome Population
2022-05-19
JGAS000532 Identification of potential blood biomarkers for early diagnosis of Alzheimer���s disease through immune landscape analysis Case-Control
2022-05-19
JGAS000533 Genomic features of renal cell carcinoma developed in end-stage renal disease and dialysis Whole Genome Sequencing
2022-05-09
JGAS000534 Comprehensive molecular and clinicopathological profiling of salivary duct carcinoma Tumor vs. Matched-Normal
2022-05-19
JGAS000535 Immuno-genomic Profiling of Biopsy Specimens Predicts Neoadjuvant Chemotherapy Response in Esophageal Squamous Cell Carcinoma Tumor vs. Matched-Normal
2022-05-22
JGAS000537 Analysis of ATL progression by CD30 signaling and its biomarkers (2) Exome Sequencing
2022-05-22
JGAS000538 Immunohistochemical and molecular pathological search in gastrointestinal tumors Tumor vs. Matched-Normal
2022-05-15
JGAS000540 New classification of occlusive cerebrovascular diseases by combining diagnostic imaging and genetic analysis of RNF213 Case-Control
2022-06-12
JGAS000541 Biobank Japan genotype data Biobank
2022-04-19
JGAS000543 Single-cell RNA-sequencing for peripheral blood mononuclear cells from COVID-19 patients and healthy controls of Japanese Case-Control
2022-07-14
JGAS000544 Whole genome, whole exome and transcriptome sequencing of 10 ccRCC with Von Hippel-Lindau disease Whole Genome Sequencing
2022-07-14
JGAS000545 Analytical study of protein function and RNA expression involved in predicting treatment efficacy and adverse event development in lung cancer radiotherapy. Cohort
2022-07-14
JGAS000546 Multimodal single-cell analyses of peripheral blood mononuclear cells in COVID-19 patients Case Set
2022-07-18
JGAS000548 Targeted Capture DNA Sequencing Targeted Capture DNA Sequencing
2022-07-21
JGAS000549 Loss of presentation of estimated neoantigens from mutated genes in ctDNA was essential for fostering primary to recurrent tumors in postoperative colorectal cancer cases Case Set
2022-07-21
JGAS000550 single-cell RNA-sequencing of human/mouse colonic crypts Transcriptome Sequencing
2022-07-25
JGAS000551 Single cell RNA sequencing of human umbilical cord blood lymphoid progenitors single cell RNA sequencing
2022-07-28
JGAS000553 Durable clinical impacts and mechanisms of action and resistance in histone K27 methylation-targeting epigenetic therapy Tumor vs. Matched-Normal
2022-08-17
JGAS000557 Research for biological features by gene expression analysis and biomarkers at diagnosis/therapeutics in lung cancer Multi-omics data
2022-08-29
JGAS000558 Target sequencing of a case of concurrent Langerhans Cell Histiocytosis and Acute Myeloid Leukemia Case Set
2022-09-19
JGAS000559 Novel compound heterozygous mutations in UHRF1 are associated with atypical immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome with distinctive genome-wide DNA hypomethylation Whole Genome Bisulfite Sequencing
2022-09-19
JGAS000561 NMR metabolic biomarkers in Biobank Japan generated by Nightingale Health Japan Biobank
2022-09-20
JGAS000562 A study of resistance to novel coronavirus infection in health care workers Cohort
2022-09-25
JGAS000563 Observational study on the immune responses acquired by COVID-19 convalescent individuals Transcriptome Sequencing
2022-09-29
JGAS000564 Analysis of genes related to the oncogenesis, progression or effectiveness of drug therapies of urological tumors . Whole Genome Sequencing
2022-10-03
JGAS000568 NGS sequencing for genes from the patients of OU Genome Project Case Set
2022-10-06
JGAS000569 The role of gut microbiota in metabolic diseases Transcriptome Sequencing
2022-10-07
JGAS000570 Whole-genome sequencing analysis for understanding of the stepwise progression of lung adenocarcinoma Whole Genome Sequencing
2022-10-06
JGAS000572 Metabolome analysis of persons with type 2 diabetes with or without diabetic complications Case-Control
2022-11-01
JGAS000573 Induction of fetal meiotic oocytes from embryonic stem cells in cynomolgus monkeys Whole Genome Sequencing
2022-11-03
JGAS000574 16S metagenomics on NASH patients complicated with diabetes Case-Control
2022-11-03
JGAS000575 Genomic features of Helicobacter pylori-na��ve diffuse-type gastric cancer. Tumor vs. Matched-Normal
2022-11-03
JGAS000578 Autoimmune-wide landscape of circulating CD4+ T cells unveils disease-specific heritability and phenotypic changes Transcriptome Sequencing
2022-11-21
JGAS000579 Target resequencing of LQTS-related 100 genes in Japanese patients Case Set
2022-11-23
JGAS000580 Building a Database of Genomic Structural Variants in Japanese population Control Set
2022-11-24
JGAS000582 Whole exome sequencing and RNA sequencing of cervical cancer Exome Sequencing
2022-11-30
JGAS000585 Establishment of xenogfafts and cultured cell lines from clinical samples Target Capture Sequencing
2022-12-15
JGAS000586 Whole exome sequencing and RNA sequencing of cervical cancer Exome Sequencing
2022-12-18
JGAS000587 Whole genome sequencing of AML with FUS-ERG Whole Genome Sequencing
2022-12-23
JGAS000588 Comprehensive biomarker analysis from phase II study of nivolumab in patients with thymic carcinoma Clinical Trial
2022-12-25
JGAS000591 Highly prevalent NF-kappa B signaling pathway-activating somatic mutations in intracranial aneurysms Case-Control
2023-01-22
JGAS000592 Germline pathogenic variant and gastric cancer risk Case-Control
2023-01-15
JGAS000593 Single-cell RNA-sequencing for peripheral blood mononuclear cells from COVID-19 patients and healthy controls of Japanese Case-Control
2023-01-30
JGAS000596 Building a Database of Genomic Structural Variants in Japanese population Control Set
2023-02-23
JGAS000597 Comprehensive analyses of genetic aberrations in cholangiolocarcinoma Exome Sequencing
2023-02-26
JGAS000598 Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases Transcriptome Sequencing
2023-02-27
JGAS000599 Comprehensive analyses of clinicopathological features and genomic mutations of combined hepatocellular-cholangiocarcinoma Exome Sequencing
2023-02-28
JGAS000600 Reconstruction of the personal information from human genome reads in gut metagenome sequencing data Population
2023-02-28
JGAS000602 Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases Transcriptome Sequencing
2023-03-08
JGAS000604 Whole genome sequencing, DNA methylation, and gene expression data from gastrointestinal stromal tumor 30 patients Whole Genome Sequencing
2023-03-12
JGAS000605 A capture methyl-seq protocol with improved efficiency and cost-effectiveness using pre-pooling and enzymatic conversion methylome analysis
2023-03-21
JGAS000609 Research for biological features by gene expression analysis and biomarkers at diagnosis/therapeutics in lung cancer Multi-omics data
2023-05-01
JGAS000610 Research for biological features by gene expression analysis and biomarkers at diagnosis/therapeutics in lung cancer Multi-omics data
2023-05-01
JGAS000611 Mitochondrial DNA Mutations at Low-level Heteroplasmy in Chronic Kidney Disease Amplicon Sequencing
2023-05-08
JGAS000617 Transcriptome sequencing of fibroblast-dependent alveolar organoids derived from patient-specific iPS cells with SFTPC^Y104H variant and their gene-corrected (monoallelic wild type SFTPC) ones. Transcriptome Sequencing
2023-06-12
JGAS000618 Development of cell lines and mouse models of bone and soft tissue sarcoma to establish novel treatment Exome Sequencing
2023-06-20
JGAS000619 Exploratory novel biomarker and resistance mechanism of milademetan, an MDM2 inhibitor, in MDM2 amplified intimal sarcoma from an open-label phase 1b/2 trial ���NCCH1806/MK004��� Case Set
2023-06-25
JGAS000621 Gene expression signatures associated with chronic endometritis revealed by RNA sequencing Transcriptome Sequencing
2023-06-29
JGAS000622 Variant allele frequency changes in TP53 predict pembrolizumab response in patients with metastatic urothelial carcinoma Target sequencing
2023-06-29
JGAS000623 Research on the identification of cancer stem cells for peidatric and adult malignancies. Case Set
2023-06-29
JGAS000625 Investigation of molecular diagnosis by molecular biological analysis using next-generation sequencer for actionable endocrine diseases (including neoplastic diseases) Parent-Offspring Trios
2023-07-12
JGAS000626 Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases Transcriptome Sequencing
2023-07-17
JGAS000627 Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases Transcriptome Sequencing
2023-07-17
JGAS000628 RNA sequencing of skin tissue and peripheral blood mononuclear cells from patients with atopic dermatitis and healthy controls. Transcriptome Sequencing
2023-07-17
JGAS000638 Study for establishment for effective screening and diagnosis of Lynch syndrome Cohort hereditary tumor
2023-09-26
JGAS000640 single-cell RNA sequencing and RNA sequencing of normal uterine cervix Transcriptome Sequencing
2023-10-11
JGAS000643 CRISPR-screening identifies mechanisms of resistance to KRASG12C and SHP2 inhibitor combinations in non-small cell lung cancer Transcriptome Sequencing
2023-10-30
JGAS000645 Whole exome sequencing of external auditory canal squamous cell carcinoma (EACSCC) Exome Sequencing
2023-10-31
JGAS000646 Genetic alterations that deregulate RB and PDGFRA signaling pathways drive tumor progression in IDH2-mutant astrocytoma Exome Sequencing
2023-11-05
JGAS000647 Asian Genome Project(BioBank Japan genotype data) Whole Genome Sequencing
2023-10-30
JGAS000648 Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases Transcriptome Sequencing
2023-11-06
JGAS000651 RNA sequencing of genetically modified human iPSCs modeling patients with autism spectrum disorders (ASD) Transcriptome Sequencing
2023-11-13
JGAS000657 Establishing stable brain tumor stem cell lines and translational research for new treatments Whole Genome Sequencing
2023-12-14
JGAS000659 CRISPR screening in human trophoblast stem cells reveals both shared and distinct aspects of human and mouse placental development Whole Genome Sequencing
2023-12-24
JGAS000661 Discovery of genetic factors associated with thiopurine-induced severe adverse events GWAS
2023-12-26
JGAS000668 Case-control study with RNA-seq transcriptome between ASD patients and non ASD controls. Transcriptome Sequencing
2024-01-29
JGAS000671 Comprehensive molecular and clinicopathological profiling of glioma Transcriptome Sequencing
2024-02-12
phs000001 National Eye Institute (NEI) Age-Related Eye Disease Study (AREDS) Case-Control
2012-01-04
phs000007 Framingham Cohort Longitudinal
2021-07-07
phs000016 International Multi-Center ADHD Genetics Project Parent-Offspring Trios
2009-11-23
phs000017 Whole Genome Association Study of Bipolar Disorder Case-Control
2008-07-13
phs000018 Search for Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (GoKinD study participants), GAIN Case-Control
2014-09-17
phs000019 Collaborative Association Study of Psoriasis Case-Control
2008-01-06
phs000020 Major Depression: Stage 1 Genomewide Association in Population-Based Samples Case-Control
2008-09-21
phs000021 Genome-Wide Association Study of Schizophrenia Case-Control
2010-10-21
phs000048 Mayo-Perlegen LEAPS (Linked Efforts to Accelerate Parkinson's Solutions) Collaboration Case-Control
2008-01-06
phs000086 Diabetes Control and Complications Trial (DCCT) and Epidemiology of Diabetes Interventions and Complications Study (EDIC) Clinical Trial
2014-08-06
phs000088 Search for Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (GoKinD study participants and parents), NIDDK Case-Control
2008-01-15
phs000089 NINDS-Genome-Wide Genotyping in Parkinson's Disease: First Stage Analysis and Public Release of Data Case-Control
2010-03-29
phs000090 The Atherosclerosis Risk in Communities (ARIC) Study Case-Cohort
2008-01-14
phs000091 GENEVA Genes and Environment Initiatives in Type 2 Diabetes (Nurses' Health Study/Health Professionals Follow-up Study) Nested Case-Control
2009-06-29
phs000092 Study of Addiction: Genetics and Environment (SAGE) Case-Control
2008-01-14
phs000093 A Genome Wide Scan of Lung Cancer and Smoking Case-Control
2009-10-07
phs000094 International Consortium to Identify Genes and Interactions Controlling Oral Clefts Case Set
2008-01-14
phs000095 Dental Caries: Whole Genome Association and Gene x Environment Studies Case-Control
2021-06-14
phs000096 Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study - Maternal Glycemia and Birthweight GEI Study Prospective
2011-08-29
phs000100 The Finland-United States Investigation of NIDDM Genetics (FUSION) Study Case-Control
2011-04-10
phs000101 Mega-GWAS ALS I Case-Control
2018-03-01
phs000102 Ischemic Stroke Genetics Study (ISGS) Case-Control
2008-01-06
phs000103 Genome-Wide Association Studies of Prematurity and Its Complications Nested Case-Control
2008-01-14
phs000122 Whole Genome Association Study of Systemic Lupus Erythematosus Case-Control
2008-01-15
phs000124 Neuroblastoma Genome-Wide Association Study (NBL-GWAS) Case-Control
2010-12-09
phs000125 CIDR: Collaborative Study on the Genetics of Alcoholism Case Control Study Case-Control
2008-02-25
phs000126 CIDR: Genome Wide Association Study in Familial Parkinson Disease (PD) Case-Control
2016-02-08
phs000127 A Genome-Wide Association Study of Sporadic ALS in an Irish Population (SIALS) and Sequencing and Analysis of an Irish Human Genome Case-Control
2010-09-02
phs000128 GAW16 Framingham and Simulated Data Longitudinal
2010-07-20
phs000130 NIDDK IBD Genetics Consortium Crohn's Disease Genome-Wide Association Study Case-Control
2008-03-16
phs000138 GWAS for Genetic Determinants of Bone Fragility in European-American Premenopausal Women Quantitative Cross-Sectional
2010-04-28
phs000139 International Multiple Sclerosis Genomics Consortium (IMSGC) Genome Wide Association Study of Multiple Sclerosis Parent-Offspring Trios
2008-05-13
phs000140 A Whole Genome Association Search for Type 2 Diabetes Genes in African Americans Case-Control
2008-06-26
phs000142 A Whole Genome Association Scan for Myopia and Glaucoma Endophenotypes using Twin Studies Twin
2008-07-17
phs000143 Starr County Health Studies' Genetics of Diabetes Study Case-Control
2008-07-14
phs000144 National Human Genome Research Institute Tumor Sequencing Project (TSP) - Lung Adenocarcinoma Tumor vs. Matched-Normal
2008-08-17
phs000145 POPRES: Population Reference Sample Population
2013-03-05
phs000147 Cancer Genetic Markers of Susceptibility (CGEMS) Breast Cancer Genome-wide Association Study (GWAS) - Primary Scan: Nurses' Health Study - Additional Cases: Nurses' Health Study 2 Case-Control
2015-02-18
phs000153 FHS-Net Social Networks Longitudinal
2015-07-05
phs000159 Genomics of Acute Myeloid Leukemia Tumor vs. Matched-Normal
2022-12-29
phs000160 National Institute on Aging (NIA) Late-Onset Alzheimer's Disease Genetics Initiative: The Multiplex Family Study Family
2008-10-16
phs000166 National Heart, Lung, and Blood Institute SNP Health Association Asthma Resource Project (SHARP) Longitudinal
2009-07-20
phs000167 Molecular Genetics of Schizophrenia - nonGAIN Sample (MGS_nonGAIN) Case-Control
2008-11-03
phs000168 National Institute on Aging - Late Onset Alzheimer's Disease Family Study: Genome-Wide Association Study for Susceptibility Loci Family
2012-03-28
phs000169 Whole Genome Association Study of Visceral Adiposity in the Health Aging and Body Composition (Health ABC) Study Longitudinal
2008-12-15
phs000170 A Genome-Wide Association Study on Cataract and HDL in the Personalized Medicine Research Project Cohort Case-Control
2012-08-01
phs000171 A Case-Controlled Study for Genotype-Phenotype Associations in Multiple Sclerosis (MS) Case-Control
2009-02-02
phs000178 National Institutes of Health The Cancer Genome Atlas (TCGA) Tumor vs. Matched-Normal
2019-12-02
phs000179 Genetic Epidemiology of COPD (COPDGene) Funded by the National Heart, Lung, and Blood Institute Case-Control
2017-11-14
phs000180 Type 1 Diabetes Genetics Consortium (T1DGC): Genome-Wide Association Study in Type 1 Diabetes, 2008 Case Set
2014-07-31
phs000181 Genomewide Association Study of Alcohol Use and Alcohol Use Disorder in Australian Twin-Families (OZ-ALC GWAS) Twin
2009-02-26
phs000182 Age related Macular Degeneration (AMD)-- Michigan, Mayo, AREDS, Pennsylvania (MMAP) Cohort Study: A Joint Genome Wide Association Study Case-Control
2010-03-21
phs000185 Genetic Studies in the Hutterites Cross-Sectional
2021-10-24
phs000187 High Density SNP Association Analysis of Melanoma: Case-Control and Outcomes Investigation Case-Control
2009-04-01
phs000188 Vanderbilt Genome-Electronic Records (VGER) Project: QRS Duration Case Set
2009-04-27
phs000196 Genome-Wide Association Study of Parkinson Disease: Genes and Environment Case-Control
2015-03-19
phs000199 Children's Hospital of Philadelphia (CHOP) Control Copy Number Variation (CNV) Study Control Set
2009-06-11
phs000200 Women's Health Initiative Clinical Trial and Observational Study Partial Factorial Randomized
2018-05-31
phs000201 Acquired Copy Number Alterations in Adult Acute Myeloid Leukemia Genomes Tumor vs. Matched-Normal
2014-04-07
phs000202 OMRF SLEGEN GWAS Data from European-American Women with Lupus Case-Control
2009-06-15
phs000203 A Genome-Wide Association Study of Peripheral Arterial Disease Case-Control
2009-06-16
phs000204 Genetic Analysis of Limb Malformation Disorders: Freeman Sheldon Syndrome Exome Sequencing Study (LMD-FSS) Exome Sequencing
2009-06-23
phs000205 International Standards for Cytogenomic Arrays Clinical Genetic Testing
2015-01-20
phs000206 Whole Genome Scan for Pancreatic Cancer Risk in the Pancreatic Cancer Cohort Consortium and Pancreatic Cancer Case-Control Consortium (PanScan) Case-Control
2015-07-09
phs000207 Cancer Genetic Markers of Susceptibility (CGEMS) Prostate Cancer Genome-Wide Association Study (GWAS) - Primary Scan (Stage 1) - PLCO Screening Trial Nested Case-Control
2009-07-21
phs000209 Multi-Ethnic Study of Atherosclerosis (MESA) Cohort Longitudinal
2014-04-30
phs000210 A Genome-Wide Association Study in Patients Experiencing Musculoskeletal Adverse Events on NCIC CTG Trial MA.27 Evaluating Aromatase Inhibitors as Adjuvant Therapy in Early Breast Cancer. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine. Nested Case-Control
2009-08-17
phs000211 National Institute of General Medical Sciences (NIGMS) Human Genetic Cell Repository Human Variation Panels including 100 African-Americans (HD100AA), 100 Caucasians (HD100CAU), 100 Han People of Los Angeles (HD100CHI) and 100 Mexican American Community of Los Angeles (HD100MEX) Population-Based Control Set
2009-08-23
phs000215 Genome-Wide Association Analysis of Biomarkers in the InCHIANTI and BLSA Population
2013-05-19
phs000216 International Consortium on the Genetics of Systemic Lupus Erythematosus (SLEGEN) Case-Control
2009-09-14
phs000217 Genome-Wide Association Study of Leprosy and Dapsone Hypersensitivity Syndrome (DHS) in Chinese population Case-Control
2018-11-07
phs000218 National Cancer Institute (NCI) TARGET: Therapeutically Applicable Research to Generate Effective Treatments Cohort
2023-02-15
phs000219 Multi-Site Collaborative Study for Genotype-Phenotype Associations in Alzheimer's disease and Longitudinal follow-up of Genotype-Phenotype Associations in Alzheimer's disease and Neuroimaging component of Genotype-Phenotype Associations in Alzheimer's disease Case-Control
2009-09-30
phs000220 Population Architecture using Genomics and Epidemiology (PAGE): Multiethnic Cohort (MEC) Cohort
2013-05-16
phs000221 NHLBI Family Heart Study (FamHS-Visit1 and FamHS-Visit2) Family
2009-10-25
phs000222 PREDICT-HD Huntington Disease Study Observational
2017-10-26
phs000223 Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Atherosclerosis Risk in Communities (ARIC) Longitudinal
2009-11-02
phs000224 VitGene Generalized Vitiligo Genetics Study-Phase 2 Case-Control
2016-02-10
phs000225 A Population Genomics Study Using a Disease-Targeted Cell model: Integration of eQTL
2009-11-03
phs000226 STAMPEED: Cardiovascular Health Study (CHS) GWAS to identify genetic variants associated with aging and CVD risk factors and events Longitudinal
2011-05-26
phs000228 NIH Human Microbiome Project - Core Microbiome Sampling Protocol A (HMP-A) Population-Based Control Set
2017-03-20
phs000233 Genome Wide Association Study of Asthma Case-Control
2009-12-01
phs000234 Development and Use of Network Infrastructure for High-Throughput GWA Studies Case-Control
2015-11-11
phs000235 National Cancer Institute Cancer Genome Characterization Initiative (CGCI) Cohort
2022-12-14
phs000236 Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Coronary Artery Risk Development in Young Adults (CARDIA) Longitudinal
2009-12-17
phs000237 Northwestern NUgene Project: Type 2 Diabetes Case-Control
2010-01-19
phs000238 National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study Case-Control
2010-01-31
phs000239 Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis Case-Control
2010-07-20
phs000240 National Eye Institute (NEI) Ocular Hypertension Treatment Study (OHTS) Clinical Trial
2010-02-22
phs000244 Genetic Analysis of Limb Malformation Disorders: Miller Syndrome Sequencing Study (LMD-MS) Exome Sequencing
2010-03-08
phs000245 Whole Genome Sequencing of a Triple Negative Breast Cancer Patient: Matched Primary Tumor, Normal, Metastasis and Xenograft samples Tumor vs. Matched-Normal
2010-03-11
phs000247 The Neonatal Microbiome and Necrotizing Enterocolitis Case-Control
2017-05-18
phs000248 Genetic Determinants of Viral Clearance in HCV-Infected Populations Case-Control
2010-03-25
phs000249 Abundant Quantitative Trait Loci Exist for DNA Methylation and Gene Expression in Human Brain Control Set
2013-12-05
phs000250 CALGB 80303:Genome-Wide Association Study of Advanced Pancreatic Cancer Patients - A Randomized Phase III trial of Gemcitabine Plus Bevacizumab versus Gemcitabine Plus Placebo in Patients with Advanced Pancreatic Cancer Clinical Trial
2010-03-31
phs000251 Human Microbiome Project Demonstration Study of Cutaneous Microbiome in Psoriasis Case-Control
2013-09-18
phs000252 Diet, Genetic Factors, and the Gut Microbiome in Crohn's Disease Cross-Sectional
2011-01-05
phs000253 Human Liver Cohort (HLC) Population
2010-04-18
phs000254 ARRA - NHLBI Lung Cohorts Sequencing Project: Genetic modifiers of Cohort
2012-10-03
phs000255 Effect of Crohn's Disease Risk Alleles on Enteric Microbiota Case-Control
2010-04-25
phs000256 The Vaginal Microbiome: Disease, Genetics and the Environment Twin
2019-05-13
phs000257 Metagenomic Analysis of the Structure and Function of the Human Gut Microbiota in Crohn's Disease Twin
2012-10-24
phs000258 The Thrifty Microbiome: The Role of the Gut Microbiota in Obesity in the Amish Longitudinal
2011-01-05
phs000259 Urethral Microbiome of Adolescent Males Longitudinal
2011-01-17
phs000260 Foregut Microbiome in Development of Esophageal Adenocarcinoma Case-Control
2015-09-09
phs000261 The Microbial Ecology of Bacterial Vaginosis: A Fine Scale Resolution Metagenomic Analysis Cohort
2020-10-07
phs000262 Ulcerative Colitis Human Microbiome Project (UCHMP) Longitudinal
2013-01-07
phs000263 Metagenomic study of the human skin microbiome associated with acne Case-Control
2010-05-02
phs000264 The Human Virome in Children and its Relationship to Febrile Illness Prospective
2011-03-03
phs000265 The Human Gut Microbiome and Recurrent Abdominal Pain in Children Case-Control
2011-05-03
phs000266 Skin Microbiome in Disease States: Atopic Dermatitis and Immunodeficiency Longitudinal
2013-08-21
phs000267 Autism Genome Project (AGP) Consortium - Whole Genome Association Study of over 1,500 Parent-Offspring Trios - Stage I and II Parent-Offspring Trios
2016-03-01
phs000268 Genotyping NIGMS CEPH Samples from the United States, Venezuela, and France Family
2010-05-06
phs000269 Genotyping NIGMS Chromosomal Aberration and Inherited Disorder Samples Cohort
2010-05-06
phs000272 National Institute of Arthritis and Musculoskeletal and Skin Diseases and Istanbul Faculty of Medicine Genome-wide Association Study of Behçet's Disease (Turkish) Case-Control
2010-05-18
phs000273 High-Throughput LINE-1 Retrotransposon Discovery in Humans Marker Discovery
2010-05-19
phs000274 Genome-Wide Association Study of Celiac Disease Case-Control
2010-05-20
phs000275 Brigham and Women's Hospital Multiple Sclerosis Genetic Collection Case-Control
2010-05-26
phs000276 STAMPEED: Northern Finland Birth Cohort 1966 (NFBC1966) Longitudinal
2012-12-13
phs000277 A Genome-Wide Association Study of Heroin Dependence Case-Control
2019-09-23
phs000279 NHLBI GO-ESP: Early-Onset Myocardial Infarction (Broad EOMI) Longitudinal
2012-10-10
phs000280 Atherosclerosis Risk in Communities (ARIC) Cohort Cohort
2021-07-20
phs000284 NHLBI Cleveland Family Study (CFS) Candidate Gene Association Resource (CARe) Longitudinal
2017-02-13
phs000285 Coronary Artery Risk Development in Young Adults (CARDIA) Study - Cohort Longitudinal
2013-04-18
phs000286 Jackson Heart Study (JHS) Cohort Cohort
2016-08-11
phs000287 Cardiovascular Health Study (CHS) Cohort: an NHLBI-funded observational study of risk factors for cardiovascular disease in adults 65 years or older Longitudinal
2017-12-04
phs000288 Ciliopathies Exome Sequencing Initiative Case-Control
2014-12-16
phs000289 National Human Genome Research Institute (NHGRI) GENEVA Genome-Wide Association Study of Venous Thrombosis (GWAS of VTE) Case-Control
2011-05-25
phs000290 NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Pulmonary Arterial Hypertension) Case-Control
2010-06-29
phs000291 NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Lung Health Study of Chronic Obstructive Pulmonary Disease) Longitudinal
2012-05-02
phs000292 Gene Environment Association Studies (GENEVA): Genetics of Early Onset Stroke (GEOS) Study Case-Control
2010-07-08
phs000293 The Familial Intracranial Aneurysm Linkage Study (FIA) Family Linkage
2010-07-19
phs000294 STAMPEED: Myocardial Infarction Genetics Consortium (MIGen) Case-Control
2010-07-19
phs000295 Next Generation Mendelian Genetics: Kabuki Syndrome Exome Sequencing
2017-12-10
phs000297 eMERGE Network Study of the Genetic Determinants of Resistant Hypertension Case-Control
2010-07-25
phs000298 Autism Sequencing Consortium (ASC) Case-Control
2017-12-04
phs000299 Whole genome and transcriptome sequencing of lung cancer patients and cell lines at Genentech Case Set
2012-09-30
phs000302 Genetic Study on Nephropathy in Type-2 Diabetes Case-Control
2010-08-15
phs000303 Genetic Epidemiology of Refractive Error in the KORA (Kooperative Gesundheitsforschung in der Region Augsburg) Study Cohort
2010-08-30
phs000304 Genes and Blood Clotting Study (GABC) Sibling Cohort
2018-05-01
phs000305 A Genome-Wide Association Study in Participants Experiencing Breast Cancer Events in High-Risk Postmenopausal Women Receiving Selective Estrogen Receptor Modulators on NSABP Trials P-1 and P-2. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine Nested Case-Control
2010-09-09
phs000306 A Multiethnic Genome-wide Scan of Prostate Cancer Nested Case-Control
2014-04-07
phs000308 The Primary Open-Angle Glaucoma Genes and Environment (GLAUGEN) Study Case-Control
2010-09-20
phs000309 Coronary Artery Risk Development in Young Adults (CARDIA) Study - Gene Environment Association Studies Initiative (GENEVA) Longitudinal
2011-10-18
phs000310 Discovery of Non-ETS Gene Fusions in Human Prostate Cancer using Next Generation RNA Sequencing Cohort
2010-10-19
phs000311 FusionSeq: a modular framework for finding gene fusions by analyzing Paired-End RNA-Sequencing data Cohort
2010-10-19
phs000313 SardiNIA Medical Sequencing Discovery Project Family
2014-03-05
phs000314 Genetic Associations in Idiopathic Talipes Equinovarus (Clubfoot) - GAIT Multiplex Families
2010-11-02
phs000327 NHLBI GO-ESP: Heart Cohorts Exome Sequencing Project (Siblings with Ischemic Stroke Study, SWISS) Affected Sib Pairs
2010-11-16
phs000328 Genome-Wide Analysis of Diffuse Large B-Cell Lymphoma (De Novo and Derived from the High Grade Transformation of Follicular Lymphoma) Case-Control
2021-03-30
phs000330 The Genomic Complexity of Primary Human Prostate Cancer Cohort
2010-12-05
phs000331 A Genome-Wide Association Study in Patients Experiencing Drug-Induced Long-QT Syndrome and/or Torsades de Pointes; A Collaboration Between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine Case-Control
2023-04-24
phs000332 Genome-Wide Association Study of Preterm Birth Case-Control
2016-01-27
phs000333 Family Investigation of Nephropathy and Diabetes (FIND) Study Case-Control
2010-12-08
phs000335 Genome-Wide associations of Lung Health Study (LHS) Cohort
2014-07-23
phs000336 A Genome-Wide Association Study of Lung Cancer Risk Case-Control
2010-12-26
phs000337 Genetic Basis of Developmental Disabilities Case Set
2010-12-26
phs000338 National Institute on Aging (NIA) SardiNIA Study Family
2011-01-26
phs000339 Targeted MitoExome Sequencing of Mitochondrial OXPHOS Diseases (Massachusetts General Hospital) Case Set
2013-02-04
phs000340 The genomic complexity of early T-cell progenitor acute lymphoblastic leukemia Whole Genome Sequencing
2014-04-08
phs000341 The Genetic Basis of Hypodiploid ALL Case Set
2012-09-30
phs000343 The Genomics and Randomized Trials Network (GARNET) Vitamin Intervention Stroke Prevention (VISP) Trial Clinical Trial
2020-10-07
phs000344 Genome-Wide Association Study of Amyotrophic Lateral Sclerosis in Finland Case-Control
2011-03-01
phs000345 NIDDK IBD Genetics Consortium Ulcerative Colitis Genome-Wide Association Study Case-Control
2011-03-01
phs000346 Genome-wide association study for Bladder Cancer Risk Case-Control
2014-08-17
phs000347 NHLBI GO-ESP: Family Studies (Thoracic aortic aneurysms leading to acute aortic dissections) Cohort
2011-03-07
phs000348 Towards a Genomic Understanding of Myeloma Tumor
2014-02-19
phs000349 SNPs and Extent of Atherosclerosis (SEA) Study Cross-Sectional
2011-03-13
phs000350 Fred Hutchinson Cancer Research Center - Whole-Exome Sequencing of Hereditary Prostate Cancer Families Family
2011-03-15
phs000351 National Cancer Institute Genome-Wide Association Study of Renal Cell Carcinoma Cohort
2011-03-21
phs000352 The genomic complexity of sporadic and inherited retinoblastoma with a matched orthotopic xenograft Case Set
2011-03-21
phs000353 Genome-Wide Association Studies of Prematurity and Its Complications (African American) Case-Control
2011-03-27
phs000354 NHLBI GO-ESP Family Studies: Pulmonary Arterial Hypertension Longitudinal
2011-03-27
phs000355 Genome Wide Association for Asthma and Lung Function Case-Control
2011-04-03
phs000356 Population Architecture using Genomics and Epidemiology (PAGE) Cross-Sectional
2014-08-14
phs000357 Genome-Wide Association Study in Systemic Sclerosis Case-Control
2014-02-04
phs000358 The PUWMa ( Parent-Offspring Trios
2011-04-18
phs000359 Exome sequencing and disease analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis Case Set
2011-04-27
phs000360 eMERGE Network Genome-Wide Association Study of Red Cell Indices, White Blood Count (WBC) Differential, Diabetic Retinopathy, Height, Serum Lipid Levels, Specifically Total Cholesterol, HDL (High Density Lipoprotein), LDL (Low Density Lipoprotein), and Triglycerides, and Autoimmune Hypothyroidism. Case-Control
2015-11-11
phs000361 Genome-Wide Association Studies in Upper Gastrointestinal Cancers (Asian) Case-Control
2011-05-01
phs000362 NHLBI GO-ESP: Family Studies (Familial Atrial Fibrillation) Cohort
2011-05-12
phs000364 High density copy number analysis and whole exome sequencing of unselected chronic lymphocytic leukemia cases and of paired chronic lymphocytic leukemia and Richter Syndrome cases Tumor vs. Matched-Normal
2011-09-11
phs000365 Exome Sequencing for Diseases of the Immune System: X-linked Immunodeficiency with Magnesium Defect, EBV Infection, and Neoplasia (XMEN) Case-Control
2011-05-31
phs000366 NHLBI: Genetic modifiers of sickle cell anemia severity and fetal hemoglobin expression in the Cooperative Study of Sickle Cell Disease (CSSCD) Longitudinal
2011-06-01
phs000367 NIDDK⁄CIDR Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease Family
2011-06-19
phs000368 Polycystic Ovary Syndrome (PCOS) Genetics Case-Control
2011-06-19
phs000369 Sequence Analysis of Mutations and Translocations Across Breast Cancer Subtypes Case Set
2011-06-20
phs000370 The Mutational Landscape of Head and Neck Squamous Cell Carcinoma Case Set
2014-04-09
phs000371 Genetic Modifiers of Huntington's Disease Cohort
2016-08-29
phs000372 Alzheimer's Disease Genetics Consortium (ADGC) Genome Wide Association Study -NIA Alzheimer's Disease Centers Cohort Case-Control
2011-06-29
phs000373 Osteoporotic Fractures in Men (MrOS) Cohort
2011-06-29
phs000374 Whole Genomic Sequencing of Nine Primary Colorectal Adenocarcinoma Tumor/Germline Pairs Case Set
2011-06-30
phs000375 Genome-Wide Association of Native and Post Aspirin Platelet Function Phenotypes Family
2011-06-30
phs000376 Whole Exome Sequencing in Familial Parkinson Disease Family
2011-07-05
phs000378 Epidemiological study comparing rates and risk factors for dementia in African Americans in Indianapolis and Yoruba living in Ibadan, Nigeria Community
2011-07-05
phs000379 Genetic Epidemiology Network of Arteriopathy (GENOA) Sibling Cohort
2011-07-06
phs000380 eMERGE Genome-Wide Association Studies of Obesity (Metabochip) Case Set
2011-07-06
phs000381 eMERGE Geisinger eGenomic Medicine (GeM) - MyCode Project Controls Control Set
2011-07-06
phs000382 CIDR Whole Exome Sequencing in Joubert Syndrome Cohort
2014-08-11
phs000383 Genome-Wide Association Study of Breast Cancer in the African Diaspora - the ROOT study Case-Control
2011-07-14
phs000384 Genentech whole genome and transcriptome sequencing of four hepatocellular carcinoma patients Case Set
2011-07-24
phs000385 Epigenetic Profiling of Human Colorectal Cancer Case Set
2011-07-27
phs000387 eMERGE Geisinger eGenomic Medicine (GeM) Abdominal Aortic Aneurysm Project (AAAP) Case Set
2011-08-02
phs000388 Charles R. Bronfman Institute for Personalized Medicine (IPM) BioBank Genome Wide Association Study of Cardiovascular, Renal and Metabolic Phenotypes Case-Control
2011-08-02
phs000389 GEnetics of Nephropathy - an International Effort (GENIE) GWAS of Diabetic Nephropathy in the UK GoKinD and All-Ireland Cohorts Case-Control
2011-08-02
phs000390 Genomic Wide Scans for Female Osteoporosis Genes Cohort
2011-08-03
phs000391 Determining Genetic Role in Treatment Response to Anti-Platelet Interventions (The PAPI Study) Interventional
2011-08-03
phs000392 Exome sequencing of autosomal recessive progressive external ophthalmoplegia (arPEO) Exome Sequencing
2011-08-04
phs000393 deCODE Genetics study on genes contributing to nicotine dependence in humans Case Set
2011-08-08
phs000394 Autopsy-Confirmed Parkinson Disease GWAS Consortium (APDGC) Case-Control
2011-08-09
phs000395 California Pacific Medical Center Research Breast Health Cohort Nested Case-Control
2011-08-21
phs000396 Division of Cancer Epidemiology and Genetics (DCEG) Imputation Reference Dataset Reference Set
2011-08-09
phs000397 National Institute on Aging (NIA) Long Life Family Study (LLFS) Family
2020-06-10
phs000398 National Heart Lung and Blood Institute (NHLBI) GO-ESP: Heart Cohorts Component of the Exome Sequencing Project (ARIC) Case-Cohort
2011-08-10
phs000400 National Heart Lung and Blood Institute (NHLBI) GO-ESP: Heart Cohorts Component of the Exome Sequencing Project (CHS) Case-Cohort
2011-08-11
phs000401 National Heart Lung and Blood Institute (NHLBI) GO-ESP: Heart Cohorts Component of the Exome Sequencing Project (FHS) Case-Cohort
2011-08-11
phs000402 National Heart Lung and Blood Institute (NHLBI) GO-ESP: Heart Cohorts Component of the Exome Sequencing Project (JHS) Case-Cohort
2011-08-11
phs000404 The Genetic Architecture of Smoking and Smoking Cessation Case-Control
2011-08-28
phs000405 Next Generation Mendelian Genetics: Malignant Hyperthermia Case Set
2011-08-29
phs000406 Spatiotemporal Transcriptome of the Human Brain Control Set
2011-08-30
phs000407 International Multi-Center ADHD Gene Project (IMAGE) II Case Sample Case Set
2011-08-31
phs000408 eMERGE Genome-Wide Association Studies of Obesity Case Set
2011-08-31
phs000409 The Genomic Analysis of Medulloblastoma Case Set
2011-09-12
phs000410 Whole Exome Sequencing for Colorectal Cancer Case-Control
2011-09-12
phs000413 Analysis of Somatic Mutations in Pediatric AML FAB-M7 Subtype by Whole Transcriptome Sequencing Case Set
2012-10-03
phs000414 Whole genome sequencing of core-binding factor leukemia Case Set
2011-09-15
phs000415 Whole Exome and Targeted Sequencing in Tourette Syndrome Multiplex Families Extended Pedigrees
2011-09-20
phs000416 Genetics of Cerebral Hemorrhage with Anticoagulation (GOCHA) Case-Control
2017-08-20
phs000417 BrainCloud: Data from human postmortem brain procurement for the neuropathology section Control Set
2012-01-26
phs000418 Temporal Dissection of Tumorigenesis in Primary Cancers Tumor vs. Matched-Normal
2014-04-07
phs000419 A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma Family
2011-10-03
phs000421 A Genome-Wide Association Study of Fuchs' Endothelial Corneal Dystrophy (FECD) Case-Control
2011-10-06
phs000422 NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Asthma): Genetic variants affecting susceptibility and severity Case Set
2011-10-06
phs000423 Genome wide association study for early onset coronary disease and related phenotypes (ADVANCE) Case-Control
2011-10-18
phs000424 Common Fund (CF) Genotype-Tissue Expression Project (GTEx) Reference Set
2022-04-25
phs000425 Alcohol Dependence GWAS in European- and African Americans Case-Control
2011-10-23
phs000426 SLCO1B1 Variants and Methotrexate Clearance Cohort
2011-10-25
phs000428 Health and Retirement Study (HRS) Longitudinal
2013-10-17
phs000430 Hepatitis C Antiviral Long-term Treatment Against Cirrhosis (HALT-C) Randomized Controlled Clinical Trial
2011-11-06
phs000431 GWAS for IgA Nephropathy Case-Control
2022-05-09
phs000433 The Sea Islands Genetic Network (SIGNET): Identifying genetic contributors to diabetes and dyslipidemia in African Americans Case-Control
2011-11-06
phs000434 Next Generation Mendelian Genetics: Atypical Werner Syndrome Case Set
2011-11-08
phs000435 Whole Exome Sequencing of Chronic Lymphocytic Leukemia Case Set
2015-10-18
phs000436 University of Miami Study on Genetics of Autism and Related Disorders (AutismDisorders) Multiplex Families
2011-11-16
phs000437 Next Generation Mendelian Genetics: Auriculocondylar syndrome (ACS) Parent-Offspring Trios
2011-11-16
phs000438 A Genome-Wide Association Analysis in Angiotensin-Converting Enzyme (ACE) Inhibitor-Associated Angioedema and ACE Inhibitor-Exposed Controls; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Center for Genomic Medicine Case-Control
2011-11-24
phs000439 A Genome-Wide Association Comparative Analysis of Response of AF Patients to Rate Control Therapy; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine Case-Control
2011-11-24
phs000440 Center for Craniofacial and Dental Genetics: Study of Dental Caries and Cleft Lip/Palate in Guatemala Nuclear Families
2011-11-24
phs000442 Drug Resistant Hypertension in African Americans' Exome Longitudinal
2011-12-06
phs000443 Transcriptome sequencing across a prostate cancer cohort identifies PCAT-1, an unannotated lincRNA implicated in disease progression Cohort
2011-12-20
phs000444 Italian Primary Biliary Cirrhosis Study Case-Control
2011-12-20
phs000445 Genome Variation among HIV-Resistant People with Hemophilia Case-Control
2012-01-05
phs000447 Prostate Cancer Genome Sequencing Project Case Set
2012-01-11
phs000448 Genetics of Schizophrenia in an Ashkenazi Jewish Case-Control Cohort Case-Control
2012-01-12
phs000449 Genetic Variation and Signatures of Natural Selection in Diverse Africans Control Set
2012-07-19
phs000450 Whole Exome Sequencing of Primary Mediastinal B-cell Lymphoma Case Set
2021-01-24
phs000451 NHLBI and NIA The New England Centenarian Study (NECS) Case Set
2012-01-30
phs000452 Melanoma Genome Sequencing Project Case Set
2016-12-18
phs000454 Genome-Wide Association Study of HIV-1 Host Genetics Among Injection Drug Users Case-Control
2019-12-09
phs000455 Molecular Genetic Studies of Developmental Brain Disorders Cohort
2012-02-13
phs000456 Risk Assessment of Cerebrovascular Events (RACE) Study Case-Control
2012-02-15
phs000458 NEI CIDR Methylation Profiling of Primary Open Angle Glaucoma in NEIGHBOR Samples Case-Control
2012-02-15
phs000459 Whole exome sequencing in multiplex cleft families from a consortium Case Set
2012-02-16
phs000460 Genetics of 24 hour urine composition Longitudinal Cohort
2012-02-16
phs000461 NEI CIDR Methylation Profiling of Primary Open Angle Glaucoma in GLAUGEN Samples Case-Control
2012-02-22
phs000462 T2D-GENES Project 2: San Antonio Mexican American Family Studies Family
2012-02-28
phs000472 Estrogen Receptor Positive Breast Cancer: Aromatase Inhibitor Response Study Tumor vs. Matched-Normal
2016-10-03
phs000473 Sweden-Schizophrenia Population-Based Case-Control Exome Sequencing Case-Control
2015-07-20
phs000474 Biology and Molecular Analysis of Human Hematopoiesis Genetics Probands
2015-10-21
phs000475 The molecular basis of inherited reproductive disorders Probands
2012-03-11
phs000476 Molecular defects in pseudohypoparathyroidism or related disorders Probands
2012-03-11
phs000477 Genetic defects in familial renal disorders Probands
2012-03-11
phs000478 Strabismus, CCDD and other anomalies Probands
2012-03-11
phs000479 National Heart Lung and Blood Institute Exome sequencing in SCID Parent-Offspring Trios
2012-03-14
phs000480 Identification of Cancer Predisposition Genes in Breast Cancer Families Family
2012-03-14
phs000481 Cholesterol and Pharmacogenetics (CAP) Study Clinical Trial
2016-07-11
phs000482 Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations Parent-Offspring Trios
2012-03-21
phs000483 Massachusetts General Hospital/Eisai National Institute of Mental Health (NIMH) Genetics Initiative Alzheimer's Disease GWAS - Affymetrix GeneChip Human Mapping 500K Array Set Family
2012-03-21
phs000484 Molecular genetic analysis of inherited kidney dysfunction Probands
2012-03-25
phs000485 Gene mutation and rescue in congenital diaphragmatic hernia Probands
2012-03-25
phs000486 Integration of Genomics and Transcriptomics in unselected Twins and in Major Depression Cohort
2012-03-27
phs000487 Functionally Active Copy Number Variants Associated with Prostate Cancer Risk Case-Control
2014-04-06
phs000488 Genomic Sequencing of Lung Adenocarcinoma Case Set
2016-10-06
phs000490 A Study of the Genetic Causes of Complex Pediatric Disorders Case Set
2012-04-09
phs000491 Whole-Genome and Exome Sequencing in clear-cell Renal Cell Carcinoma (ccRCC) Case Set
2012-04-12
phs000492 Genetics of Human Developmental Brain Disorders Family
2023-01-10
phs000493 Genetic Association Studies in the Solomon Islanders Case-Control
2012-04-17
phs000494 Better Outcomes for Children: GWAS from Cincinnati Children's Hospital Medical Center (CCHMC) - eMERGE Phase II data - (dbGaP Deposit 1) Cohort
2012-04-17
phs000495 The Gene Partnership (TGP) - eMERGE Data Longitudinal
2012-04-19
phs000496 Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease Case-Control
2012-04-19
phs000497 Genetic analysis of Hirschsprung disease Probands
2016-07-31
phs000500 Non-invasive whole genome sequencing of a human fetus Parent-Offspring Trios
2012-05-20
phs000501 Compilation of Aggregate Genomic Data for General Research Use Aggregate Genomic Data
2012-05-22
phs000502 Genome-Wide Analysis of Splenic Marginal Zone Lymphoma Case-Control
2012-05-28
phs000504 Medulloblastoma exome sequence analysis Case Set
2013-10-23
phs000505 Gene Fusion Discovery through RNA Sequencing of Human Glioblastoma Stem Cell Lines RNA Sequencing
2013-07-18
phs000507 NHLBI and NIDDK Sponsored GWAS in Benign Ethnic Neutropenia/Leukopenia (BEN) in African-Americans (age >45 yrs old) from the REGARDS Case-Control
2018-10-25
phs000508 Genomic Sequencing of Pediatric Rhaboid Cancers Case Set
2014-04-06
phs000509 Genome Sequencing of Hepatocellular Carcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM) Case Set
2012-06-25
phs000510 Study of Osteoporotic Fractures (SOF) Cohort
2012-06-28
phs000511 Treatment of genetic screening of hypertriglyceridemia type I, III, and V - HTG Amsterdam Probands
2012-07-05
phs000513 Rearrangements of the MAST Kinase and Notch Gene Families in Breast Cancer Cohort
2012-07-09
phs000514 Identification of Genes Involved in Familial Coronary Artery Disease Probands
2012-07-09
phs000516 Genome Sequencing of Pancreatic Ductal Adenocarcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM) Case Set
2015-02-12
phs000517 GWAS in African Americans, Latinos and Japanese Case-Control
2015-04-30
phs000518 NHLBI GO-ESP Family Studies: Idiopathic Bronchiectasis of unknown etiology that is not related to cystic fibrosis or classic primary ciliary dyskinesia or immune deficiency or any other known causes Cohort
2012-07-23
phs000519 Study of Melanoma Risk in Australia and the United Kingdom Case Set
2012-07-23
phs000521 Episodic Ataxia Syndrome: Longitudinal Study Longitudinal
2019-07-17
phs000522 Hyperdiploid Acute Lymphoblastic Leukemia RNA-Seq Case Set
2012-07-31
phs000524 National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Chronic Renal Insufficiency Cohort Study (CRIC) Cohort
2012-08-01
phs000525 Expressed Pseudogenes in the Transcriptional Landscape of Human Cancers Cohort
2012-08-06
phs000535 Whole Genome and Exon Capture Sequencing of Bladder Cancers Cohort
2012-08-12
phs000536 Somatic L1 Retrotransposition in Colorectal Tumors Case-Control
2015-07-28
phs000537 Next Generation Mendelian Genetics: Familial Hemophagocytic Lymphohistiocytosis Cohort
2012-08-23
phs000538 Next Generation Mendelian Genetics: Familial Combined Hyperlipidemia Family
2012-08-27
phs000539 Next Generation Mendelian Genetics: Congenital Hyperinsulinism Case Set
2012-08-28
phs000540 Next Generation Mendelian Genetics: Ehlers-Danlos Syndrome Type VIII Case-Control
2012-08-28
phs000541 Next Generation Mendelian Genetics: Muscle Hypertrophy Case Set
2012-08-28
phs000542 Next Generation Mendelian Genetics: Neonatal Diabetes Case Set
2012-08-28
phs000543 Exome Sequencing of Pleuropulmonary Blastoma Case Set
2012-08-28
phs000545 Predicting Chemotherapy-Induced Mucositis with Genetic and Clinical Factors Case-Control
2012-09-03
phs000546 NHLBI GO-ESP: Heart Cohorts Exome Sequencing Project (Ischemic Stroke Genetic Study, ISGS) Case-Control
2012-09-11
phs000547 A Genome-Wide Association Study in Breast Cancer Patients from the Prospectively Randomized SUCCESS Trial Prospective
2012-09-11
phs000548 Phase I Clinical Trial Describing the Pharmacogenomics of Aspirin Cohort
2012-09-27
phs000549 Clonal Evolution of Pre-Leukemic Hematopoietic Stem Cells Precedes Human Acute Myeloid Leukemia Case Set
2012-09-27
phs000550 Genome-Wide Characterization of Pancreatic Adenocarcinoma Patients Using Next Generation Sequencing Case Set
2012-09-27
phs000551 Gene Expression Signatures in CATHGEN Case-Control
2012-09-30
phs000552 Genomic Characterization of Meningiomas Case Set
2014-04-06
phs000553 Familial Exome Sequencing in Rare Pediatric Phenotypes Parent-Offspring Trios
2012-10-02
phs000554 Mutational Landscape of Lethal Castrate Resistant Prostate Cancer Tumor vs. Matched-Normal
2012-10-02
phs000556 NHLBI GO-ESP: Family Studies (JHMI-Molecular Genetics of Atypical Cystic Fibrosis (CF) Study) Case-Control
2012-10-08
phs000558 National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study: Whole Exome Resequencing in Glaucoma Case Set
2012-10-11
phs000559 Population Architecture Using Genomics and Epidemiology (PAGE): Epidemiologic Architecture for Genes Linked to Environment (EAGLE) - BioVU Cancer Project Case-Control
2012-10-15
phs000560 Ecological Stressors, PTSD, and Drug Use in Detroit: The Detroit Neighborhood Health Study (DNHS) Cohort
2021-04-28
phs000561 Metabolism and Genetics of Hypobetalipoproteinemia Probands
2012-10-25
phs000562 The Genetic Landscape of Mutations in Burkitt Lymphoma Tumor vs. Matched-Normal
2012-10-25
phs000563 The Genomics of Pilocytic Astrocytoma Formation in Neurofibromatosis Type 1 Case Set
2022-12-12
phs000564 Rapid Whole Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units Case Set
2014-11-16
phs000565 Copy Number Variation in Congenital Kidney Malformations Case Set
2012-11-05
phs000567 Identification of Recurrent NAB2-STAT6 Gene Fusions in Solitary Fibrous Tumor by Integrative Sequencing Case Set
2012-11-29
phs000568 Genomic Sequencing of Solitary Fibrous Tumors Case Set
2012-12-03
phs000571 National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Pediatric Cardiac Genetics Consortium (PCGC) Cohort
2015-07-29
phs000572 Alzheimer's Disease Sequencing Project (ADSP) Case-Control
2016-06-08
phs000573 Genetic Heterogeneity of Diffuse Large B Cell Lymphoma Case-Control
2012-12-18
phs000574 Angelman, Rett, Prader-Willi Syndrome Consortium (ARP) Rett Syndrome Natural History Protocol Case Set
2012-12-27
phs000575 Prader-Willi Syndrome and Early-onset Morbid Obesity Natural History Protocol Case Set
2020-02-11
phs000576 Angelman, Rett, Prader-Willi Syndromes Consortium (ARP) Angelman Syndrome Natural History Protocol Case Set
2019-07-21
phs000577 Longitudinal Study of Urea Cycle Disorders Longitudinal
2012-12-30
phs000578 Non Dystrophic Myotonias: Genotype-Phenotype Correlation and Longitudinal Longitudinal
2013-01-02
phs000579 Small Intestine Neuroendocrine Tumors (Carcinoid Tumors) Case Set
2013-01-03
phs000580 Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Strong Heart Study (SHS) and Strong Heart Family Study (SHFS) Longitudinal Cohort
2013-01-07
phs000581 NHLBI GO-ESP: Family Studies (Dilated Cardiomyopathy) Case Set
2013-01-07
phs000582 NHLBI GO-ESP: Family Studies (Familial Interstitial Pneumonia) Family
2013-01-07
phs000583 Asian Indian Diabetic Heart Study (AIDHS) /Sikh Diabetes Study (SDS) Case-Control
2013-01-09
phs000584 The Longevity Genes Project Case-Control
2013-01-09
phs000585 International Consortium for Blood Pressure (ICBP) Meta-Analysis
2016-08-02
phs000586 Genome Wide Association Studies in Alopecia Areata Case Set
2013-01-23
phs000587 NHLBI GO-ESP: Family Studies (Mendelian Lipid Disorders) Case Set
2013-01-28
phs000588 VCRC - Giant Cell Arteritis Longitudinal Study Longitudinal
2013-01-29
phs000589 Rare Diseases Clinical Research Network (RDCRN) Vasculitis Clinical Research Consortium (VCRC) Longitudinal Protocol for Takayasu's Arteritis Longitudinal
2013-01-29
phs000590 Rare Diseases Clinical Research Network (RDCRN) Vasculitis Clinical Research Consortium (VCRC) Longitudinal Protocol for Polyarteritis Nodosa Longitudinal
2013-01-30
phs000592 Screening Protocol and Longitudinal Study of Bone Marrow Failure Syndromes and Cytopenias Longitudinal
2013-01-30
phs000594 A Phase 2 Study of Tipifarnib in Large Granular Lymphocyte (LGL) Leukemia Interventional
2013-01-31
phs000595 Mucociliary Clearance Consortium (MCC) Rare Genetic Disorders of the Airways: Cross-section Comparison of Clinical Features, and Development of Novel Screening and Genetic Test Cross-Sectional
2013-01-31
phs000596 Mucociliary Clearance Consortium (MCC) Longitudinal Study of Primary Ciliary Dyskinesia: Participants 5-18 Years of Age Longitudinal
2019-07-17
phs000597 DNA Methylation Analysis of Prostate Cancer Cell Lines and Tissues Using Next Generation Sequencing Case-Control
2013-01-31
phs000598 Exome Sequencing of Esophageal Adenocarcinoma Case Set
2013-10-21
phs000600 Genomic Sequencing of Cervical Cancers Case-Control
2013-02-14
phs000601 Filtering and Annotation of Variants That Are Rare (FAVR) Family
2013-02-14
phs000602 Identification of Targetable FGFR Gene Fusions in Diverse Cancers Case Set
2014-04-07
phs000603 Rare Genetic Steroid Disease Consortium (GSD) Apparent Mineralocorticoid Excess (AME) Syndrome Natural History Clinical Protocol Case Set
2013-02-27
phs000604 Mapping Genes for Mammographic Density Population
2013-03-10
phs000605 Multicenter International Lymphangioleiomyomatosis Efficacy of Sirolimus Trial (The MILES Trial) Clinical Trial
2013-03-11
phs000606 The Incidence of Thromboembolic Events in Patients with Antibodies to Heparin-PF4 after Cardiac Bypass Longitudinal
2013-03-11
phs000607 Neurodevelopmental Genomics: Trajectories of Complex Phenotypes Cohort
2018-03-07
phs000608 Whole Genome Profiling to Detect Schizophrenia Methylation Markers Case-Control
2013-03-25
phs000609 RNA-Seq studies of Gene Expression in Cells and Networks in FI and ACC in Autism Case-Control
2013-03-28
phs000611 Whole Genome Comparisons of Breast Cancers and their Xenotransplants Case Set
2013-04-03
phs000612 The mutational characterization of adenoid cystic carcinoma Case-Control
2013-04-16
phs000614 Genomic Analysis of Pediatric Low Grade Gliomas Case Set
2013-04-17
phs000615 The National Institute of Neurological Disorders and Stroke (NINDS) Stroke Genetics Network (SiGN) Case-Control
2013-04-22
phs000616 CIP: Obesity-Diabetes Familial Risk, Viva La Familia Study Cohort
2015-04-14
phs000617 PGRN-Leducq: Identification of the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes Case-Control
2013-04-29
phs000618 Genome-Wide Association Study of Hypertriglyceridemia in Mexicans Case-Control
2013-05-07
phs000619 DNA Methylation Analysis of Peripheral Blood Cells from Siblings Discordant for ASD Case-Control
2013-05-09
phs000620 Minnesota Center for Twin and Family Research (MCTFR) Genome-Wide Association Study of Behavioral Disinhibition Longitudinal
2013-05-16
phs000621 Genome Wide Association Studies in ECOG 2997 Trial Clinical Trial
2013-05-16
phs000622 FaceBase Study of Facial Shape in Tanzania: CIDR Clinical Trial
2013-05-16
phs000623 Rare Mendelian Disease in Old Order Amish and Mennonite Patients Case Set
2013-05-19
phs000624 The Lung Genomics Research Consortium (LGRC) Cohort
2013-05-22
phs000625 Targeted Sequencing of GWAS Loci in Cleft Lip and Palate Parent-Offspring Trios
2013-05-30
phs000626 CD4+ cell transcriptional profiling by RNA sequencing Control Set
2013-06-12
phs000627 University of North Carolina at Chapel Hill (UNC) Hepatocellular Carcinoma Study by Exome Sequencing (HCCSES) Case Set
2013-06-13
phs000628 Characterization of a Metastatic Cervical Cancer Patient and HPV18 Integration Using Next Generation Sequencing Case Set
2013-06-13
phs000629 Genetic Epidemiology of Lung Cancer Consortium GWAS of Familial Lung Cancer Case-Control
2013-06-24
phs000630 Exome Chip Study of NIMH Controls Control Set
2013-06-25
phs000631 ARDSnet and the iSPAAR Consortium: Genomic Basis of Susceptibility and Outcomes in Patients with the Acute Respiratory Distress Syndrome (ARDS) Case-Control
2013-06-25
phs000632 NHLBI GO-ESP: Family Studies (Hematological Cancers) Family
2013-06-26
phs000633 Enrichment of Lung Microbiome with Supraglottic Taxa which is Associated with Increased Pulmonary Inflammation Cross-Sectional
2013-06-26
phs000634 National Cancer Institute (NCI) Genome Wide Association Study (GWAS) of Lung Cancer in Never Smokers Case-Control
2013-06-27
phs000636 Whole Exome Sequencing for Familial Intracranial Aneurysm (FIA I-II) Study Family
2013-07-11
phs000637 Methotrexate Clearance GWAS in Acute Lymphoblastic Leukemia (ALL) Patients Cohort
2013-07-21
phs000638 Genome-Wide Association Study of Relapse of Childhood Acute Lymphoblastic Leukemia Cohort
2013-07-21
phs000639 Human Autism Genetics Case-Control
2023-04-05
phs000640 HeLa Cell Genome Sequencing Studies Whole Genome Sequencing
2020-10-12
phs000641 Whole Exome Sequencing Identifies Family
2013-07-22
phs000644 The Effect of the Menstrual Cycle on DNA Expression in the Normal Human Breast Epithelium Observational
2013-07-24
phs000645 Location and Function of NSun2-Mediated Cytosine-5 Methylation in RNA and its Effect on Translation Case-Control
2019-03-20
phs000646 Breakpoint detection using long insert whole genome sequencing Case Set
2013-08-01
phs000647 Study of Adaptation to Hypoxia in Ethiopian Highlanders via Whole Genome Sequencing Cohort
2013-08-04
phs000648 Pancreatic Cancer Case Control Association Study Case-Control
2013-08-05
phs000649 Pharmacogenomic Evaluation of Antihypertensive Responses (PEAR and PEAR-2) Prospective
2016-10-12
phs000650 Pediatric Investigation of Genetic Factors Linked with Renal Progression (PediGFR): Chronic Kidney Disease in Children Cohort (CKiD) Cohort
2013-08-11
phs000652 Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan) Cohort
2013-08-12
phs000653 Epi4K: Gene Discovery in 4,000 Epilepsy Genomes Parent-Offspring Trios
2016-08-02
phs000655 Genetics of Inherited Muscle Disease Probands
2016-01-14
phs000656 Genetic measurement of memory B-cell recall using antibody repertoire sequencing Longitudinal
2013-08-22
phs000657 A Pilot Study Using Next Generation Sequencing in Advanced Cancers: Feasibility and Challenges Case Set
2013-08-25
phs000658 MDD2000AFFY Case Set
2013-08-26
phs000659 Characterization of the Gut-Associated Microbiome in Inflammatory Pouch Complications Following Ileal Pouch-Anal Anastomosis Case-Control
2013-08-28
phs000660 Chinese Alternating Hemiplegia of Childhood (AHC) Disease Study Parent-Offspring Trios
2013-08-29
phs000661 Germline Sequencing for Aggressive Prostate Carcinoma Case Set
2013-09-05
phs000662 National Children's Study Vanguard Study Formative Research Study (NCS) Cohort
2013-09-10
phs000663 Drug-Induced Liver Injury Network (DILIN) Case Set
2021-08-05
phs000664 Characterization of Autosomal CNV Among the Negrito from Peninsular Malaysia Population
2013-09-19
phs000666 B and T Cell Determinants of Influenza Vaccine Responses in the Elderly Longitudinal
2013-09-26
phs000669 The African American Breast Cancer Epidemiology and Risk (AMBER) Consortium Study Case-Control
2013-09-29
phs000670 Pharmacogenomics Research Network Antidepressant Medication Pharmacogenomic Study (PGRN-AMPS) Prospective
2013-09-29
phs000671 Somatic Mutations in Variant and IGHV4-34 Expressing Hairy Cell Leukemia Case Set
2013-10-17
phs000672 National Institute of Dental and Craniofacial Research (NIDCR) Sjögren's International Collaborative Clinical Alliance (SICCA): Center for Inherited Disease Research (CIDR) Genome-Wide Genotyping Multicenter
2013-10-17
phs000673 University of Michigan Clinical Sequencing Exploratory Research (CSER) Case Set
2019-02-27
phs000674 Resource for Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort
2013-10-22
phs000676 Sequence-Based Analysis of Human Breast Tumors Tumor vs. Matched-Normal
2016-07-26
phs000677 An APOBEC Cytidine Deaminase Mutagenesis in Human Cancers Meta-Analysis
2013-10-31
phs000678 The Two Sister Study: A Family-Based Study of Genes and Environment in Young-Onset Breast Cancer Family
2013-11-04
phs000679 Genome-Wide Association Study of Anorexia Nervosa (Price Foundation, Klarman Family Foundation, Center for Applied Genomics at the Children's Hospital of Philadelphia, Scripps Translational Sciences Institute Clinical Translational Science Award) Case-Control
2013-11-04
phs000681 Common Variation in Candidate Genes in the Diabetes Prevention Program Clinical Trial
2018-03-19
phs000682 Genetics of Neuropsychiatric and Neurodevelopmental Disorders Multiplex Families
2013-11-11
phs000684 Age related Macular Degeneration (AMD) - Michigan, Mayo, AREDS, Pennsylvania (MMAP) Cohort Study: Association and Sequencing Studies Case-Control
2013-11-20
phs000687 Bulgarian Trio Sequencing Study to Identify de Novo Mutations in Schizophrenia Parent-Offspring Trios
2013-11-25
phs000689 Genomic Analysis of Peripheral T-Cell Lymphomas Case-Control
2013-12-11
phs000690 Whole-Genome Sequencing in Multiplex Epilepsy Families Family
2013-12-11
phs000691 CIP: Differential Response to Hydroxyurea and Incidence of Stroke in Sickle Cell Disease Case-Control
2014-12-01
phs000692 A Pharmcogenetic Study of Bipolar Disorder in a Taiwanese Han Chinese Population (TWBP) Case Set
2013-12-15
phs000693 University of Washington Center for Mendelian Genomics (UW-CMG) Mixed
2019-02-28
phs000694 Clinical Cancer Sequencing Case Set
2017-08-06
phs000695 A Phase I/II Trial of Sirolimus (Rapamune®) and Cyclosporine in Patients with Refractory Aplastic Anemia Clinical Trial
2014-01-05
phs000697 Mechanism and Response of Thymoglobulin in Patients with Myelodysplastic Syndrome (MDS) Clinical Trial
2014-01-06
phs000698 QUANTitative Chest Computed Tomography UnMasking Emphysema Progression in Alpha-1 Antitrypsin Deficiency Clinical Trial
2014-01-06
phs000699 Osteosarcoma Genomics Case Set
2014-01-06
phs000700 NIH Roadmap Epigenomics Program - Broad Institute Epigenetics
2019-09-23
phs000701 Efficacy of a Therapeutic Treatment Trial in Angelman Syndrome Prospective
2014-01-06
phs000703 CATHeterization GENetics (CATHGEN) Longitudinal
2014-01-12
phs000706 Genome Sequencing Reveals That RAD50 Hypomorphism Results in Enhanced Sensitivity to Checkpoint Kinase Inhibition Combined with Chemotherapy Case Set
2014-01-21
phs000707 Next Generation Mendelian Genetics: Hereditary Neurological Disorders Case Set
2016-11-03
phs000708 Warfarin Pharmacogenetics: Pharmacogenetic Optimization of Anticoagulant Response (POAT) and Genetic and Environmental Determinants of Warfarin Response (GEDWR) Cohort
2014-01-23
phs000709 Genomic and Transcriptomic Landscape of Fibrolamellar Hepatocellular Carcinoma Cohort
2014-01-26
phs000710 1000 Genomes Used for Cloud Testing Reference Set
2014-02-04
phs000711 Baylor Hopkins Center for Mendelian Genomics (BH CMG) Mixed
2020-12-20
phs000712 University of Illinois at Chicago (UIC) Autism Centers of Excellence (ACE) Exome Sequencing Analysis Parent-Offspring Trios
2014-02-10
phs000713 Glial Cell Line-Derived Neurotrophic Factor (GDNF) Polymorphisms and Anxiety, Depression Cross-Sectional
2014-02-11
phs000714 NICHD Genomic and Proteomic Network for Preterm Birth Research (GPN) Case-Control
2014-02-11
phs000715 NINDS Deep Sequencing for the Detection of Viral Sequences in Primary Progressive Multiple Sclerosis Brains Case-Control
2014-02-13
phs000716 Genome-Wide Association Study of Lung Cancer Susceptibility in Never-Smoking Women in Asia Case-Control
2014-02-13
phs000717 Genomics of Circulating Tumor Cells Case Set
2014-02-13
phs000718 Trisomy21: Risk Factors for Chromosome Nondisjunction (T21NDJ) Parent-Offspring Trios
2014-02-16
phs000719 Genetic Basis of Pulmonary Non-tuberculous Mycobacterial Infections Family
2014-02-16
phs000720 Genomic sequencing of Pediatric Rhabdomyosarcoma Case Set
2021-03-15
phs000721 NIH Undiagnosed Diseases Program (UDP) Genotypic and Phenotypic Study Parent-Offspring
2014-02-20
phs000722 Whole Exome Sequencing of Colorectal Cancer Patients from the Nurses' Health Study (NHS) and Health Professionals Follow-up Study (HPFS) Case Set
2020-10-07
phs000723 Sequencing of Cervical Cancer Case-Control
2014-03-04
phs000725 Rare Cancer Tumors Project Cohort
2017-01-23
phs000726 Genome-wide Association Study of Myasthenia Gravis Case-Control
2014-03-11
phs000727 Profiles of extracellular miRNA in cerebrospinal fluid and serum from patients with Alzheimer's or Parkinson's disease correlate with disease status and features of pathology Case-Control
2014-03-16
phs000728 The Genetics of Lung Cancer Susceptibility in Smokers Family
2014-03-17
phs000729 Solution-based exome capture and HiSeq2000-based massively parallel sequencing of Follicular Lymphoma Case Set
2014-03-17
phs000730 Genomics of Brain Metastases Case Set
2014-03-18
phs000732 L1-Seq and Genome-Wide SNP Genotyping in a Multiethnic Asian Population Cohort
2014-03-24
phs000733 The International Consortium for Prostate Cancer Genetics Genome Wide Association Study of Familial Prostate Cancer Case-Control
2014-03-26
phs000734 A Genome-wide Association Study (GWAS) of Risk for Osteosarcoma Case Set
2014-03-31
phs000735 The Placenta Harbors a Unique Microbiome Case-Cohort
2014-04-06
phs000737 The National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Genetics of Genetic Epidemiology of Metabolic Syndrome in an Island Population Cross-Sectional
2014-04-15
phs000738 Exome Sequencing in Schizophrenia Families Parent-Offspring Trios
2014-04-16
phs000739 Identification of Recurrent SMO and BRAF Mutations in Ameloblastomas Cohort
2014-04-16
phs000740 Whole Genome Sequencing of Waldenstrom's Macroglobulinemia Case-Control
2014-04-20
phs000741 Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) Lipidomics Study Longitudinal
2015-10-26
phs000742 The Epilepsy Phenome/Genome Project Parent-Offspring Trios
2014-04-29
phs000743 METSIM (METabolic Syndrome In Men) Study Cohort
2017-02-06
phs000744 Yale Center for Mendelian Genomics (YCMG) Mixed
2021-06-15
phs000745 ADCC Pilot RNAseq Study on Posterior Cingulate Astrocytes in Alzheimer's Disease Case-Control
2014-05-06
phs000747 Whole Exome and Transcriptome Sequencing in Sporadic ALS Case-Control
2017-05-11
phs000748 Relating Clinical Outcomes in Multiple Myeloma to Personal Assessment of Genetic Profile Longitudinal
2018-12-30
phs000750 Genomic Origins and Admixture in Latinos (GOAL) Parent-Offspring Trios
2014-05-22
phs000751 GWAS in Fibrosing Interstitial Lung Disease Case-Control
2014-05-22
phs000753 High Density SNP Association Analysis of Lung Cancer Case-Control
2014-05-28
phs000755 BrainSpan Atlas of the Human Brain Control Set
2018-11-13
phs000756 Exome Sequencing to Identify Medically Relevant Associations in Finnish Sub-Isolate Samples from the FINRISK Cohort Longitudinal
2014-06-05
phs000757 Ataxia Gene Identification by Integrated Genomic Analysis Family
2014-06-09
phs000758 Family Genomics of Congenital Heart Defects Family
2014-06-10
phs000759 The spectrum of somatic mutations in high-risk acute myeloid leukemia with -7/del(7q) Tumor vs. Matched-Normal
2014-06-11
phs000760 Human Responses to Influenza Vaccination Case-Control
2014-06-15
phs000761 Orofacial Pain: Prospective Evaluation and Risk Assessment (OPPERA) Case-Control
2014-06-19
phs000763 The Collaborative Study on the Genetics of Alcoholism (COGA) Family
2014-06-19
phs000766 GEI Studies - Psoriasis Case-Control
2014-06-24
phs000767 The UC San Diego Chronic Lymphocytic Leukemia (CLL) Study Tumor vs. Matched-Normal
2014-06-24
phs000768 Genomic sequencing of Ewing's Sarcoma Case Set
2016-10-02
phs000769 National Heart, Lung, and Blood Institute (NHLBI) Data Coordinating Center, Microbiome of the Lung and Respiratory Track, Lung HIV Microbiome Project (LHMP) Observational
2014-06-25
phs000770 Somatic Mutation Profile by Next Generation Sequencing in HER2+ Breast Cancer Cohort
2014-06-29
phs000771 Bladder Chemotherapy Responders Case-Control
2017-10-23
phs000772 Genetic Predictors of Adverse Radiotherapy Effects (Gene-PARE) Cohort
2014-06-29
phs000774 Center for Craniofacial and Dental Genetics (CCDG): Genetics of Orofacial Clefts and Related Phenotypes Parent-Offspring
2017-10-16
phs000775 Transcriptome study of differential expression in schizophrenia Case-Control
2014-07-06
phs000776 Consanguinity and rare mutations outside of MCCC genes underlie non-specific phenotypes of MCC Deficiency Case-Control
2014-07-08
phs000777 National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Gene Discovery in Autosomal Dominant Focal Segmental Glomerulosclerosis (FSGS) Case Set
2014-07-10
phs000778 National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK): Identification of VUR genes by exome sequencing Case Set
2014-07-16
phs000779 Ontario Familial Colon Cancer Registry Single Nucleotide Polymorphisms and CpG Methylation (OFCCR SNP-CpG) Case-Control
2014-07-21
phs000781 Children's Hospital of Philadelphia: GWAS of Left-Sided Cardiac Defects Parent-Offspring Trios
2014-07-28
phs000782 Post-liver transplant recurrent human hepatocellular carcinoma study (RHCCS) Longitudinal
2014-07-29
phs000783 Whole Exome Sequencing of Congenital Diaphragmatic Hernia Patients and Trios Case Set
2017-03-16
phs000784 Genetic Epidemiology Network of Salt Sensitivity (GenSalt) Family
2019-11-14
phs000785 Exome Sequencing Analysis of Cutaneous Squamous Cell Carcinoma Cohort
2014-08-12
phs000787 Immunosenescence: Immunity in the Young and Aged Cohort
2014-08-13
phs000788 Research Program on Genes, Environment and Health (RPGEH) Cohort
2017-10-15
phs000789 Collaborative Study of Genes, Nutrients and Metabolites (CSGNM) Control Set
2014-08-17
phs000790 Comparative Sequence Analysis Between Primary and Metastatic Colorectal Cancer Lesions Cohort
2014-08-19
phs000791 Integrated Epigenetic Maps of Human Embryonic, Extraembryonic and Adult Cells Control Set
2019-12-09
phs000792 Oncogenomics of Malignant Peripheral Nerve Sheath Tumors Case Set
2014-08-24
phs000793 Paired Acute Myeloid Leukemia (AML) Epigenetics Study on Epialleles and Clonality Cohort
2014-08-26
phs000794 Longitudinal genome-wide analysis of progressive chronic lymphocytic leukemia under uniform front-line therapy of pentostatin, cyclophosphamide, and rituximab Longitudinal
2014-09-02
phs000795 Gastric Cancer Genetic Analysis of Metastasis Case-Control
2014-09-02
phs000796 Genome Wide Association Study of Chronic TMD: Discovery Phase Case-Control
2014-09-02
phs000797 Immune Dysregulation in Human Subjects with Heterozygous Germline Mutations in Case Set
2014-09-02
phs000798 Performance Characteristics of Selective Targeted Enrichment in Genetic Diagnostic Testing Control Set
2014-09-04
phs000799 Shanghai Breast Cancer Genetics Study (SBCGS) Case-Control
2014-09-10
phs000801 National Cancer Institute (NCI) Non-Hodgkin Lymphoma Genome-wide Association Study (GWAS) Cohort
2016-01-04
phs000803 Gastrointestinal Cancer Treatment Responders Longitudinal
2016-11-13
phs000804 Genomic Sequencing of Ewing Sarcoma Whole Genome Sequencing
2014-09-22
phs000806 Myocardial Infarction Genetics Exome Sequencing Consortium: Ottawa Heart Study Case-Control
2014-09-25
phs000807 Study on longer adjuvant chemotherapy in Women with Early Breast Cancer Cohort
2014-09-28
phs000808 PGRN/PAT: The genomic basis for susceptibility to drug-induced long QT syndrome (diLQTS) Case-Control
2014-09-30
phs000809 Autosomal Recessive PGM3 Mutations Link Glycosylation Defects to Atopy, Immune Deficiency, Autoimmunity, and Neurocognitive Impairment Parent-Offspring Trios
2014-09-30
phs000810 Hispanic Community Health Study /Study of Latinos (HCHS/SOL) Cohort
2014-10-02
phs000811 Comparison of Custom Capture for Targeted Next Generation DNA Sequencing Mixed
2014-10-02
phs000812 The Breast and Prostate Cancer Cohort Consortium (BPC3) GWAS of Aggressive Prostate Cancer and ER- Breast Cancer Case-Control
2014-10-05
phs000813 CIDR, NCI, NIDA Sequencing of Targeted Genomic Regions Associated with Smoking Case-Control
2014-10-06
phs000814 Myocardial Infarction Genetics Exome Sequencing Consortium: Italian Atherosclerosis Thrombosis and Vascular Biology Case-Control
2014-10-07
phs000815 Gene Expression and Regulatory Networks in Human Leukocytes - Immunological Variation Consortium Control Set
2020-01-29
phs000816 Characterization of X Chromosome Inactivation Using Integrated Analysis of Whole-Exome and mRNA Sequencing Parent-Offspring Trios
2016-04-18
phs000817 Responses to Varicella Zoster Virus Vaccination Cohort
2014-10-15
phs000819 The Normal Human Tissue Sequencing Project: Non-Diseased, Non-Malignant Tissues Control Set
2014-10-16
phs000820 The Cleveland Clinic Foundation's (CCF) Lone Atrial Fibrillation (AFIB) GWAS Study Case Set
2023-01-10
phs000821 DNA Methylation age and mortality in the Lothian Birth Cohorts of 1921 and 1936 Longitudinal Cohort
2014-10-20
phs000822 Genome-Wide Discovery of Novel Breast Cancer Predisposing Mutations Case Set
2014-10-20
phs000823 Discovery of Novel Melanoma Predisposing Mutations by Exome Sequencing Case Set
2014-10-21
phs000824 Genome-Wide Discovery of Novel Colon Cancer Predisposing Mutations Case Set
2014-10-21
phs000825 Whole Genome Sequencing of Harvard University Embryonic Stem Cell Lines 63 and 64 Control Set
2014-10-23
phs000826 Prediction of Trastuzumab Benefit in Adjuvant Breast Cancer: Gene Expression Profiling in NSABP B31 Clinical Trial
2014-10-27
phs000827 North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing (NCGENES) Case Set
2016-08-31
phs000828 Genomic Analysis of Fibrolamellar Hepatocellular Carcinoma Case Set
2014-11-03
phs000830 Xeroderma Pigmentosum, Complementation Group C, (XPC) and Non-XPC Cutaneous Squamous Cell Carcinoma (cSCC) Mutation Rate Study Cohort
2014-11-05
phs000831 Sporadic Amyotrophic Lateral Sclerosis (ALS): Parent-Offspring and Twin Sequencing Study Parent-Offspring Trios
2014-11-12
phs000832 Sensitivity to the Subjective Effects of Amphetamine Cohort
2014-11-12
phs000833 Single Cell Analysis Program - Transcriptome (SCAP-T) Case Set
2017-08-03
phs000837 Whole Genome Sequencing of Two Family Trios with 22q.11.2 Deletion Syndrome Parent-Offspring Trios
2014-11-16
phs000838 Ghana Prostate Study Case-Control
2014-11-16
phs000839 Efficacy of Bitter Taste Blockers on Flavor Acceptance in a Human Population Control Set
2014-11-17
phs000840 The Genetics of Type 2 Diabetes Consortium (GoT2D): Low-Pass Sequencing and High-Density SNP Genotyping for Type 2 Diabetes Case-Control
2014-11-20
phs000841 Sanger sequencing of catalytic-domain encoding exons of tyrosine kinase genes from human endometrial tumor DNAs Case Set
2014-11-25
phs000842 Pediatric Investigation for Genetic Factors Linked with Renal Progression (PediGFR) Cohort
2017-10-15
phs000845 Genomic Factors Involved in Chromosome Rearrangements Cohort
2014-11-30
phs000846 Whole Genome Bisulfite Sequencing of Circulating Cell-Free (CCF) DNA and its Cellular Contributors Cross-Sectional
2014-12-01
phs000847 T2D-GENES Consortium: San Antonio Mexican American Family Studies (SAMAFS) Family
2016-08-03
phs000848 Autosomal recessive Case-Control
2014-12-02
phs000851 African American Breast Cancer GWAS Case-Control
2015-01-04
phs000852 GEDI: A Developmental Model of Gene-Environment Interplay in SUDs: Combined Genotype Dataset from the "Great Smoky Mountains Study" and the "Caring for Children in the Community Study". Case-Control
2015-01-04
phs000853 Normative Aging Study (NAS) Longitudinal Cohort
2022-01-26
phs000855 Resistance studies in Lung Cancer Case-Control
2015-01-07
phs000856 Chromothripsis in Patient WHIM-09 Single Patient
2015-01-11
phs000857 Primary ER-positive Breast Cancer Treated with Neoadjuvant Letrozole Clinical Trial
2015-01-12
phs000858 Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing Parent-Offspring Trios
2015-01-13
phs000862 Lysosomal Disease Network (LDN6719) Immune Response to Intrathecal Enzyme Therapy in Mucopolysaccharidosis 1 Patients Observational
2015-01-26
phs000863 National Cancer Institute (NCI) Genome-Wide Association Study (GWAS) of Renal Cell Carcinoma in African Americans Case-Control
2015-01-26
phs000864 Genomic Predictors of Combat Stress Vulnerability and Resilience Longitudinal Cohort
2015-02-01
phs000866 Family Genomics of Bipolar Disorder Family
2015-02-03
phs000867 The Finland-United States Investigation of NIDDM Genetics (FUSION) Study Case-Control
2015-02-05
phs000868 Transcriptome Sequencing of Pediatric Neuroblastoma Case Set
2015-02-09
phs000869 Barrett's and Esophageal Adenocarcinoma Genetic Susceptibility Study (BEAGESS) Case-Control
2015-02-10
phs000870 Characterization of Human Transcriptome by Computational and HTS Approaches Control Set
2015-02-19
phs000871 Whole Exome Sequencing of Pancreatic Neuroendocrine Tumors at The Human Genome Sequencing Center, Baylor College of Medicine (HGSC-BCM) Cohort
2015-02-23
phs000872 Autism Post-Mortem Brain RNA-Sequencing: SRRM4 Splicing Study Case-Control
2015-02-23
phs000873 Exome Sequencing of a family with thrombocytopenia, red cell macrocytosis, and lymphoblastic leukemia predisposition Family
2015-02-24
phs000874 Genetic and Environmental Risk Factors for Hemorrhagic Stroke (GERFHS) Case-Control
2015-02-25
phs000876 Transdisciplinary Research Into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing Case-Control
2018-09-04
phs000879 Dana-Farber Cancer Institute (DFCI) Brown Lab CLL Sequencing Study Cohort
2020-06-29
phs000882 National Cancer Institute (NCI) Prostate Cancer Genome-Wide Association Study for Uncommon Susceptibility Loci (PEGASUS) Case-Control
2015-03-08
phs000883 Myocardial Infarction Genetics Exome Sequencing Consortium: Precocious Coronary Artery Disease Study Case-Control
2015-03-11
phs000884 Gut microbiome profiles according to sex, body mass index and dietary fiber intake Control Set
2015-03-16
phs000885 CAGE Profiling of ncRNAs in Hepatocellular Carcinoma Reveals a Strong Activation of Retroviral LTR Promoters in Virus-Induced Tumors Case-Control
2015-03-17
phs000886 An Omics View of Asthma through Monozygotic Twins Case-Control
2015-03-17
phs000888 eMERGE Network Imputed GWAS for 41 Phenotypes Case-Control
2015-03-18
phs000892 Clinical Proteomic Tumor Analysis Consortium (CPTAC) Proteogenomic Confirmatory Study of Breast, Colon, Lung, and Ovarian Tumors Case Set
2017-02-06
phs000893 Genome-Wide Association Study of Endometrial Cancer in the Epidemiology of Endometrial Cancer Consortium (E2C2) Case-Control
2015-03-26
phs000894 Genome Wide Association Study of Serum Creatinine during Vancomycin Therapy and Vancomycin Pharmacokinetics Cohort
2015-03-30
phs000895 Integrated Genomic Analysis of Periampullary Tumors at The Human Genome Sequencing Center, Baylor College of Medicine (HGSC-BCM) Cohort
2015-03-31
phs000896 Functional Dynamics of the Elderly Gut Microbiome During Probiotic Consumption Longitudinal
2015-04-01
phs000897 Mayo Clinic and Illumina Collaborative Early Stage Ovarian Cancer (ESOC) Study Case Set
2015-04-02
phs000898 Megabase-scale Haplotyped Genomic Analysis of Normal and Cancer Genomes Case Set
2022-12-12
phs000899 National Institute of Mental Health (NIMH) Amish Mennonite Bipolar Genetics Study (AmBiGen) Family
2015-04-06
phs000900 Functionally-defined Therapeutic Targets in Diffuse Intrinsic Pontine Glioma (DIPG) Cohort
2015-04-08
phs000901 University of Washington Cerebrospinal Fluid Biomarker Study for Parkinson disease Case-Control
2015-04-16
phs000902 Myocardial Infarction Genetics Exome Sequencing Consortium: Registre Gironi del Cor Case-Control
2015-04-19
phs000903 OCD Collaborative Genetic Association Study (OCGAS) Parent-Offspring Trios
2015-04-21
phs000904 Novel APC Promoter and Exon 1B Deletion and Allelic Silencing in Three Mutation-Negative Classic Familial Adenomatous Polyposis Families Mendelian
2015-04-21
phs000906 eMERGE Network's Multi-Center Pilot of Pharmacogenetic Sequencing in Clinical Practice Cohort
2015-04-26
phs000907 Next Generation Sequencing of Stage IV Squamous Cell Lung Cancers Reveals an Association of PI3K Aberrations and Evidence of Clonal Heterogeneity in Patients with Brain Metastases Case Set
2015-04-27
phs000908 University of Miami Udall Center of Excellence Identification of Rare Variants in PD through Whole Exome Sequencing Case-Control
2015-04-29
phs000909 Molecular Basis of Neuroendocrine Prostate Cancer (Trento/Cornell/Broad 2015) Cohort
2015-04-30
phs000910 Type 1 Diabetes Genetics Consortium (T1DGC): Copy Number Variant (CNV) Study Affected Sib Pairs
2015-05-03
phs000911 Type 1 Diabetes Genetics Consortium (T1DGC): ImmunoChip Study Case-Control
2015-05-03
phs000912 San Francisco Bay Area Latina Breast Cancer Study Case-Control
2015-05-03
phs000913 Genomic Analysis of Mycosis Fungoides and Sézary Syndrome Identifies Recurrent Alterations in TNFR2 Tumor vs. Matched-Normal
2015-05-05
phs000914 Genome-wide Association Study of Adiposity in Samoans Cross-Sectional
2015-05-05
phs000915 Stand Up To Cancer East Coast Prostate Cancer Research Group Case Set
2016-04-18
phs000916 Myocardial Infarction Genetics Exome Sequencing Consortium: German Heart Center in Munich Case-Control
2015-05-18
phs000917 Myocardial Infarction Genetics Exome Sequencing Consortium: Pakistan Risk Of Myocardial Infarction Study Case-Control
2015-05-18
phs000918 International Parkinson's Disease Genomics Consortium (IPDGC), NeuroX Dataset Case-Control
2015-05-18
phs000920 NHLBI TOPMed - NHGRI CCDG: Genes-Environments and Admixture in Latino Asthmatics (GALA II) Case Set
2020-10-07
phs000921 NHLBI TOPMed: Study of African Americans, Asthma, Genes and Environment (SAGE) Case-Control
2019-11-17
phs000922 Genetic Aberrations and Subclonal Structure Impact Chronic Lymphocytic Leukemia Longitudinal
2021-05-13
phs000923 Molecular Characterization of Germ Cell Tumors Cohort
2015-05-28
phs000924 NextGen Consortium: The iPSCORE (iPSC Collection for Omic Research) Resource for Studying the Impact of Genetic Variation on Molecular Phenotypes Control Set
2019-07-18
phs000925 PAGE: The Charles Bronfman Institute for Personalized Medicine (IPM) BioMe BioBank Longitudinal Cohort
2015-05-31
phs000926 Rare Disease Susceptibility Alleles in Children with Crohn Disease Family
2015-06-02
phs000927 CSER: Clinical Implementation of Carrier Testing Using Next Generation Sequencing (NextGen) Randomized
2015-06-04
phs000928 Transcriptomic Profile of Whole Blood Cells from Elderly Subjects fed Probiotic Bacteria Lactobacillus rhamnosus GG ATCC 53103 (LGG) in a Phase I Open Label Study Longitudinal
2015-06-04
phs000929 High-Risk Breast Cancer GWAS Case-Control
2015-06-08
phs000930 CHARGE (Cohorts for Heart and Aging Research in Genomic Epidemiology) Consortium Summary Results from Genomic Studies Cohort
2022-01-01
phs000931 DMET Genes, Nicotine Metabolism and Prospective Abstinence Family
2015-06-10
phs000932 A Somatic Reference Standard for Cancer Genome Sequencing Tumor vs. Matched-Normal
2015-06-14
phs000933 Genomic Profiling of Melanoma Case Set
2021-11-03
phs000934 Antibody Repertoires in CVID Case-Control
2015-06-15
phs000935 The CHOP Pediatric Genetic Sequencing (PediSeq) Project : Applying Genomic Sequencing in Pediatrics Cross-Sectional
2015-06-15
phs000936 NHLBI GO-ESP: Early-Onset Myocardial Infarction Exome Chip (Broad EOMI) Case-Control
2015-06-15
phs000937 The Landscape of Antisense Gene Expression in Human Cancers Cohort
2015-06-15
phs000938 Evaluation of Hybridization Capture versus Amplicon-based Methods for Whole Exome Sequencing Control Set
2015-06-15
phs000939 Detection of Enhancer-Associated Rearrangements Reveals Mechanisms of Oncogene Dysregulation in B-cell Lymphoma Case Set
2017-08-14
phs000941 Phylogenetic Analyses of Melanoma Reveal Complex Patterns of Metastatic Dissemination Tumor vs. Matched-Normal
2015-06-22
phs000942 Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic Cohort
2015-06-23
phs000944 eMERGE Phase III Clinical Center at Partners HealthCare Cross-Sectional
2015-06-28
phs000945 Genomic Characterization of African-American Prostate Cancer Cohort
2015-06-29
phs000946 NHLBI TOPMed: Boston Early-Onset COPD Study Probands
2022-11-17
phs000947 Genome-Wide Assessment of DNA Methylation in Systemic Lupus Erythematosus-Related Autoantibodies Case Set
2015-06-30
phs000948 Genetic Discovery and Application in a Clinical Setting: Continuing a Partnership (eMERGE Phase II) Cohort
2015-06-30
phs000949 Genetic Analysis of Normal Human Facial Variation Control Set
2015-07-01
phs000950 Surveillance, Epidemiology and End Results (SEER) Formalin Fixed Paraffin Embedded (FFPE) Tissue Feasibility Study Case Set
2015-07-05
phs000951 NHLBI TOPMed: Genetic Epidemiology of COPD (COPDGene) Case-Control
2020-10-07
phs000952 Substance Dependence GWAS in European- and African - Americans Case-Control
2015-07-09
phs000953 Microdissected Pancreatic Cancer Whole Exome Sequencing Longitudinal Cohort
2015-07-09
phs000954 NHLBI TOPMed: The Cleveland Family Study (CFS) Longitudinal
2020-10-07
phs000955 Genetic Components of Knee Osteoarthritis (GeCKO) Study: The Osteoarthritis Initiative Longitudinal
2015-07-09
phs000956 NHLBI TOPMed: Genetics of Cardiometabolic Health in the Amish Family
2020-10-07
phs000957 Geisinger Health System - MyCode, eMERGE III Exome Chip Case-Control
2015-07-15
phs000958 National Human Genome Research Institute (NHGRI) Clinical Sequencing Exploratory Research (CSER) The MedSeq Project: Integration of Whole Genome Sequencing into Clinical Medicine (HG006500) Case-Control
2015-07-17
phs000959 Exome Sequencing of Schizophrenia Cases and Controls in the South African Xhosa Population Case-Control
2015-07-20
phs000960 Biomarkers in Transplant Recipients Case Set
2020-02-11
phs000961 eMERGE III: Columbia GENIE (Genomic Integration with EHR) Case-Control
2015-07-20
phs000962 Exploring the Genetic Variants Associated with Brain Growth in Children Case Set
2015-07-21
phs000963 PGRN-RIKEN: Genetic Determinants of Clinical Cardiovascular Events in Patients Receiving Statins Case-Control
2015-07-22
phs000964 NHLBI TOPMed: The Jackson Heart Study (JHS) Longitudinal Cohort
2020-10-07
phs000966 National Institute of Neurological Disorders and Stroke (NINDS), Family Study of Essential Tremor (FASET), Identification of Susceptibility Genes for Essential Tremor Multiplex Families
2023-02-15
phs000967 Exome Sequencing of Clear Cell Endometrial Tumors and Paired Non-tumor Samples Case Set
2015-07-28
phs000968 The Cardiopulmonary Effects of Particulate Exposure Longitudinal
2019-11-04
phs000969 Whole Exome Sequencing of One Nuclear Family with Non-syndromic Sensorineural Hearing Loss Parent-Offspring
2015-08-02
phs000970 The Influence of Gut Microbiota on the Speciation and Toxicity of Mercury During Pregnancy Cross-Sectional
2015-08-03
phs000971 The ClinSeq Project: Piloting Large-Scale Genome Sequencing for Research in Genomic Medicine Case Set
2021-05-26
phs000972 NHLBI TOPMed: Genome-Wide Association Study of Adiposity in Samoans Cross-Sectional
2020-10-07
phs000973 The Genomic Landscape of Juvenile Myelomonocytic Leukemia Collection
2015-08-09
phs000974 NHLBI TOPMed: Genomic Activities such as Whole Genome Sequencing and Related Phenotypes in the Framingham Heart Study Cohort
2020-10-07
phs000975 The Nurses' Health Study (NHS) GWAS of Mammographic Density Case-Control
2015-08-12
phs000976 Study on the Genetics of Alcoholism (COGA): African American Family GWAS Family
2020-08-23
phs000977 Genetic Analysis of Desmoplastic Melanoma Tumor vs. Matched-Normal
2015-08-18
phs000978 Whole-Genome Sequencing (WGS) of a Malignant Granular Cell Tumor (GCT) with Metabolic Response to Pazopanib Case-Control
2015-08-20
phs000979 HBCC Postmortem Psychiatric Molecular Studies Case-Control
2019-09-05
phs000980 Mutational Landscape Determines Sensitivity to PD-1 Blockade in Non-Small Cell Lung Cancer Cohort
2015-08-24
phs000981 Lactobacillus rhamnosus GG ATCC (LGG) as an immune adjuvant for influenza vaccination in the elderly Longitudinal
2015-08-25
phs000982 Genetic Analysis of Psoriasis and Psoriatic Arthritis: GWAS of Psoriatic Arthritis Case-Control
2015-08-31
phs000983 Pharmacogenomics of Rheumatoid Arthritis Therapy Case Set
2015-08-31
phs000984 Pharmacogenomics of Metformin Dose Response in T2DM Patients Case Set
2015-08-31
phs000985 Functional Significance of Prostate Cancer Risk-SNPs Cohort
2022-02-15
phs000986 Genetic Basis of Cryptorchidism Case-Control
2015-09-03
phs000987 Whole exome sequencing of 184 unrelated subjects with 22q11.2 deletion syndrome (DiGeorge syndrome/velo-cardio-facial syndrome) Case Set
2015-09-07
phs000988 NHLBI TOPMed: The Genetic Epidemiology of Asthma in Costa Rica Parent-Offspring Trios
2020-10-07
phs000989 Cellular Diversity of the Developing Human Cerebral Cortex Cohort
2023-05-21
phs000990 Myocardial Infarction Genetics Exome Sequencing Consortium: University of Lubeck Case-Control
2015-09-17
phs000991 VESPA: Vanderbilt Electronic Systems for Pharmacogenomic Assessment Cohort
2015-09-21
phs000993 NHLBI TOPMed: Heart and Vascular Health Study (HVH) Case Set
2021-05-09
phs000994 The Mutational Landscape of CTCL and Sezary Syndrome Longitudinal Cohort
2015-09-23
phs000996 Genome-Wide Environment Interaction Study on Neurodevelopment in Children from Mexico and Bangladesh Cohort
2019-08-12
phs000997 NHLBI TOPMed - NHGRI CCDG: The Vanderbilt AF Ablation Registry Case Set
2021-05-09
phs000998 RNA Sequencing of Pulmonary Arterial Endothelial Cells in Pulmonary Hypertensive Patients and Controls Case-Control
2016-05-01
phs000999 Clinical Sequencing Exploratory Research (CSER): Clinical sequencing in cancer: Clinical, ethical, and technological studies Longitudinal
2019-11-21
phs001000 Myocardial Infarction Genetics Exome Sequencing Consortium: U. of Leicester Case-Control
2015-09-30
phs001001 Massachusetts General Hospital (MGH) Atrial Fibrillation Study Case Set
2015-09-30
phs001002 A Genome-Wide Association Study of CALGB 90401: Randomized, Double-Blind, Placebo-Controlled Phase III Trial Comparing Docetaxel and Prednisone with or without Bevacizumab in Men with Metastatic Castration-Resistant Prostate Cancer Cohort
2015-10-07
phs001003 Prospective Procurement of Solid Tumor Tissue to Identify Novel Therapeutic Targets Cohort
2022-02-23
phs001004 Genetic Analysis of Parkinson's Disease Parent-Offspring Trios
2015-10-13
phs001005 Identification of Putative Neoantigens in Stage III Melanoma Case Set
2016-01-03
phs001006 Lobular Carcinomas In Situ Display Intra-Lesion Genetic Heterogeneity and Clonal Evolution in the Progression to Invasive Disease Prospective
2015-10-14
phs001007 The Genetic Landscape of Metastasis and Recurrence in Head and Neck Squamous Cell Carcinoma Case Set
2015-10-19
phs001008 GUARDIAN: The Insulin Resistance Atherosclerosis Family Study (IRASFS) Family
2015-10-19
phs001009 Determinants of Asthma Following RSV Bronchiolitis in Early Life Prospective
2015-10-21
phs001011 Cincinnati Children's Hospital Medical Center (CCHMC) - eMERGE Phase IIIA Data Cohort
2020-07-20
phs001012 The Diabetes Heart Study (DHS) Cross-Sectional
2015-10-26
phs001013 Heart and Vascular Health Study (HVH) Case-Control
2017-08-20
phs001014 GUARDIAN: The Insulin Resistance Atherosclerosis Study (IRAS Classic) Cohort
2015-10-26
phs001015 Genome Wide Association Study of Subjects with Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS) Case-Control
2015-10-26
phs001016 Fixed single-cell transcriptomic characterization of human radial glial diversity Single Cell Analysis
2015-10-27
phs001017 Breast Cancer Susceptibility Case Set
2015-10-27
phs001018 Molecular Characterization of Clinical Renal Tumors Cohort
2015-10-27
phs001020 Genomic Psychiatry Cohort (GPC) Whole Genome Sequencing and Genotyping Study Case-Control
2019-08-07
phs001021 CHDWB Rare Regulatory Alleles and Gene Expression Study Cohort
2015-10-28
phs001022 PsychENCODE Consortium: Epigenetic and Transcriptional Dysregulation in Autism Spectrum Case-Control
2015-10-28
phs001023 Male Infertility: Genetics of Spermatogenic Failure Case-Control
2015-10-28
phs001024 NHLBI TOPMed: Partners HealthCare Biobank Case Set
2022-11-14
phs001025 GWAS in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture Case-Control
2015-11-01
phs001026 Baylor College of Medicine Advancing Sequencing in Childhood Cancer Care (BASIC3) Clinical Exome Sequencing Study - Clinical Sequencing Exploratory Research Consortium Longitudinal
2015-11-01
phs001027 Epigenomics Studies in Acute Myeloid Leukemia (AML) Cohort
2021-06-08
phs001028 Complete Genomics Deep Whole-Genome Sequencing of Circulating Tumor Cells from a Patient with Metastatic Breast Cancer Case Set
2015-11-05
phs001030 Viral Respiratory Pathogens Genetics Cohort
2015-11-08
phs001032 NHLBI TOPMed: The Vanderbilt Atrial Fibrillation Registry (VU_AF) Case Set
2021-05-10
phs001033 PAGE: Global Reference Panel Control Set
2015-11-15
phs001034 New England-Based Case-Control Study of Ovarian Cancer Case-Control
2015-11-16
phs001036 Comprehensive Genomic Characterization of Acral Melanoma Tumor vs. Matched-Normal
2015-11-23
phs001037 The Environmental Determinants of Diabetes in the Young Study (TEDDY) Longitudinal
2015-11-24
phs001038 Inhibiting DNA Methylation Causes an Interferon Response in Cancer via dsRNA Including Endogenous Retroviruses Case Set
2015-12-02
phs001039 International Age-Related Macular Degeneration Genomics Consortium - Exome Chip Experiment Case-Control
2015-12-02
phs001040 NHLBI TOPMed: Novel Risk Factors for the Development of Atrial Fibrillation in Women Case Set
2022-11-15
phs001041 Genetic Basis for Clinical Response to CTLA-4 Blockade in Melanoma Longitudinal Cohort
2015-12-13
phs001043 A Genome-Wide Association Study in Patients Experiencing Breast Events While Receiving Adjuvant Aromatase Inhibitors for Early Breast Cancer on NCIC CTG Trial MA.27 Case-Control
2015-12-14
phs001044 Breast Cancer Risk Pathways Case-Control
2015-12-16
phs001045 Molecular Epidemiology of Colorectal Cancer (MECC) Metastasis Study: A Germline Variant on Chromosome 4q31.1 Associates with Susceptibility to Developing Colon Cancer Metastasis Case Set
2015-12-16
phs001046 Genomic Architecture of Progression and Treatment Response in AMD Case-Control
2015-12-17
phs001048 The Finland-United States Investigation of NIDDM Genetics (FUSION) Tissue Biopsy Study Cohort
2018-12-30
phs001049 Genomics of Relapsed Small Cell Lung Cancer Progression Case Set
2015-12-21
phs001050 Breast Cancer Genome Guided Therapy Study (BEAUTY) Case Set
2015-12-21
phs001052 Modelling Multi-Dimensional ClinOmics for Precision Therapy of Children and Adolescent Young Adults with Relapsed and Refractory Cancer: A Report from the Center for Cancer Research Cohort
2019-12-12
phs001053 National Eye Institute (NEI) Exfoliation Genotyping Study Case Set
2015-12-22
phs001054 Genomic Characterization of Pediatric Low-Grade Gliomas Case Set
2015-12-27
phs001055 Whole Genome Study for De Novo Mutation Rates Parent-Offspring Trios
2015-12-29
phs001057 Population Genetics Analysis Program: Immunity to Vaccines/Infections - Smallpox Vaccination (NIAID/NIH) Cohort
2016-01-04
phs001058 Myocardial Infarction Genetics Exome Sequencing Consortium: BioImage Study Case-Control
2016-01-05
phs001059 Maternal Plasma Folate and DNA Methylation in Epigenome-Wide Meta-Analysis of Newborns Longitudinal
2016-01-12
phs001062 NHLBI TOPMed - NHGRI CCDG: Massachusetts General Hospital (MGH) Atrial Fibrillation Study Case Set
2021-05-10
phs001063 Genomic Characterization of Patient-Derived Xenograft Models to Improve Targeted Therapy for HER2+ Breast Cancer Brain Metastases Treatments Case Set
2016-01-28
phs001064 Whole Exome Sequencing of Six Signet Ring/Plasmacytoid Variant Bladder Tumors Cohort
2016-01-28
phs001065 Coenzyme Q10 (CoQ) in Huntington's Disease (HD) (2CARE) Multicenter
2016-01-28
phs001066 Whole Genome, Exome, Transcriptome and Validation Sequencing of an Acute Lymphoblastic Leukemia Case Set
2016-01-28
phs001067 Metagenomic Deep Sequencing in Meningitis and Encephalitis Case Set
2016-01-31
phs001071 NINDS Family-Based Whole-Genome Sequencing to Find Modifiers of Age of Onset in Huntington's Disease Case-Control
2016-02-09
phs001072 Mechanisms of Therapy Driven Clonal Evolution in Oncogenic RAS Mutant Relapsed Acute Lymphoblastic Leukemia Cohort
2016-02-11
phs001073 Epigenetic Analysis of Malnutrition Clinical Trial
2022-01-30
phs001074 GeneSTAR (Genetic Study of Atherosclerosis Risk) NextGen Consortium: Functional Genomics of Platelet Aggregation Using iPS and Derived Megakaryocytes Longitudinal Cohort
2016-02-21
phs001075 Sequencing to Guide Cancer Care (CanSeq) Case Set
2016-02-22
phs001076 Inflammatory Bowel Disease Exome Sequencing Study Case Set
2016-02-22
phs001078 Common Variant GWAS, Genetics & Epidemiology of Colorectal Cancer Consortium (GECCO) Case-Control
2016-02-25
phs001079 Transcriptional Profiling of PD-1+ and PD-1- Teff and Treg Cells in Glioblastoma and Health Case-Control
2017-08-23
phs001080 Genome Studies in Hereditary Spastic Paraplegia Case Set
2016-02-29
phs001082 Zostavax vaccination-induced changes in the T cell receptor repertoire to varicella zoster virus Longitudinal
2016-03-01
phs001083 99 Cases of Small Cell Lung Cancer Study Case Set
2016-03-01
phs001084 Differential Mutations in Matched Primary and Metastatic Colorectal Cancers Case Set
2016-03-03
phs001085 Genetic History of Neandertal and Denisovan Introgression into Melanesian Individuals Population
2016-03-03
phs001087 Common Deleterious Germline Variants Shape the Urothelial Cancer Genome Case Set
2020-02-10
phs001088 Shanghai Breast Cancer Genetics Study (SBCGS) Case-Control
2016-03-13
phs001089 HudsonAlpha Institute for Biotechnology Clinical Sequencing Exploratory Research (CSER): Genomic Diagnosis in Children with Developmental Delay Family
2021-01-18
phs001090 Genome-wide Association Study for Non-syndromic Clefts in the African Population: CIDR Case-Control
2016-03-17
phs001091 Clonal Evolution in Patients with Chronic Lymphocytic Leukemia Longitudinal
2016-03-17
phs001093 Type 2 Diabetes Genetic Exploration by Next-generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: London Life Sciences Population Study (LOLIPOP) UK South Asian Case-Control
2016-03-24
phs001095 Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: Ashkenazi Case-Control
2016-03-27
phs001096 Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: KARE Case-Control
2016-03-27
phs001097 Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: Singapore Case-Control
2016-03-27
phs001101 Myocardial Infarction Genetics Exome Sequencing Consortium: Malmo Diet and Cancer Study Case-Control
2016-03-28
phs001105 NHGRI-Mayo Clinic Whole Genome Sequencing of Aggressive Prostate Tumors Case-Control
2016-04-06
phs001106 Genomics of Hepatocellular Carcinoma Case Set
2016-04-07
phs001107 Patient-Specific Factors Influence Somatic Variation Patterns in Von Hippel-Lindau Disease Renal Tumors Tumor vs. Matched-Normal
2016-04-10
phs001108 Assessing Neural Mechanisms of Injury in Inborn Errors of Urea Metabolism Using Structural MRI, Functional MRI, and Magnetic Resonance Spectroscopy Case-Control
2016-04-12
phs001109 Addictions: Genotypes, Polymorphisms, and Function/Human Genetic Correlates of Addictive Diseases Case-Control
2020-02-24
phs001110 Kids First: Pediatric Research Project on the Genomic Analysis of Congenital Diaphragmatic Hernia Parent-Offspring Trios
2020-08-25
phs001111 A Multi-Gene Mutation Classification of 468 Colorectal Cancers Reveals a Prognostic Role for APC Case Set
2016-04-21
phs001112 Chromosome X Mosaicism Methylation Study Case Set
2016-05-02
phs001115 Melanoma and Cancer-Associated Fibroblast Short-Term Cultures Derived from Patient Metastases Case Set
2016-05-02
phs001119 Subpopulations and Intermediate Outcome Measures in COPD Study (SPIROMICS) Longitudinal Cohort
2016-05-09
phs001120 ELLIPSE Prostate Cancer Meta-Analysis and Genotyping Case-Control
2020-12-07
phs001121 Integrated Genetic and Pharmacologic Interrogation of Rare Cancers Cohort
2016-05-12
phs001122 Genome-wide Identification of Variants Affecting Early Human Brain Development Cohort
2016-05-15
phs001123 Consortium on Asthma among African-ancestry Populations in the Americas (CAAPA) Population Genomics
2019-02-20
phs001124 Mechanisms of Risk for Sulfonamide Hypersensitivity Case-Control
2016-05-17
phs001127 Genomic Analysis of Paired Endometrial Cancer Primaries and Metastases Case Set
2016-05-19
phs001130 NIDDM-Atherosclerosis Study (NIDDM-Athero) Cohort
2016-05-22
phs001133 Follow-up of Ovarian Cancer Genetic Association and Interaction Studies (FOCI) Case-Control
2016-05-23
phs001134 Radiation-Related Genomic Profile of Papillary Thyroid Cancer after the Chernobyl Accident Case Set
2022-10-25
phs001135 Starting Treatment with Agonist Replacement Therapies (START): A Randomized Trial of Methadone vs Buprenorphine/Naloxone for the Treatment of Opioid Dependence Longitudinal
2020-02-26
phs001138 National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Gabriella Miller Kids First Pediatric Research Program of the Pediatric Cardiac Genetics Consortium (PCGC) Cohort
2021-09-01
phs001139 NextGen Consortium: GENESiPS Study: Identifying the Gene Networks of Insulin Resistance Case-Control
2016-06-06
phs001140 ALCHEMIST Study Case Set
2016-06-06
phs001141 PROstate Cancer Medically Optimized Genome Enhanced ThErapy (PROMOTE) of Castration Resistant Prostate Cancer (CRPC) Patients Treated with Abiraterone Acetate Case Set
2022-08-02
phs001143 NHLBI TOPMed: The Genetics and Epidemiology of Asthma in Barbados Family
2020-10-07
phs001145 Exceptional Responders Initiative Case-Control
2016-06-08
phs001146 Expression Quantitative Trait Locus Mapping Studies in Mid-Secretory Phase Endometrial Cells Identifies HLA-F and TAP2 as Fecundability-Associated Genes eQTL
2016-06-08
phs001151 Region-specific Transcriptome Analysis of the Human Retina and Retinal Pigment Epithelium (RPE)/Choroid Control Set
2016-06-13
phs001152 Somatic Mutational Analysis by Exome Sequencing Endometrial Carcinosarcomas Case Set
2016-06-15
phs001153 Somatic Mutational Analysis by Exome Sequencing Late-Stage Endometrioid Endometrial Carcinoma Case Set
2016-06-15
phs001154 Indexing Genes Impacted by Copy Number Variation in Developmental Disorders Case-Control
2016-06-15
phs001156 The EVE Asthma Genetics Consortium: Building Upon GWAS Case-Control
2017-08-20
phs001157 Wisconsin Longitudinal Study on Aging Longitudinal Cohort
2016-06-20
phs001158 Human Dorsal Root Ganglion RNA Landscape Profiling for Neuropathic and Chronic Pain Case-Control
2019-01-30
phs001159 Genomic Profiling of Sequentially Acquired Metastatic Sites from an "Exceptional Responder" Lung Adenocarcinoma Patient Reveals Extensive Genomic Heterogeneity and Novel Somatic Variants Case Set
2016-06-21
phs001163 CRU-Ukrainian National Research Center for Radiation Medicine Trio Study Parent-Offspring Trios
2016-06-26
phs001164 The Role of Germline Mutation and Parental Age in Autism Spectrum Disorders Parent-Offspring Trios
2016-06-29
phs001165 eMERGE: Genetics of Complex Pediatric Disorders from the Center for Applied Genomics Longitudinal Cohort
2016-06-30
phs001166 Type 2 Diabetes Starr County GWAS and Exome Sequencing Case-Control
2016-07-05
phs001167 Type 2 Diabetes in African Americans, GWAS and Exome Sequencing Case-Control
2016-07-05
phs001168 Kids First: Genomic Studies of Orofacial Cleft Birth Defects Parent-Offspring Trios
2019-02-25
phs001169 Integrative Analysis of Lung Adenocarcinoma in EAGLE (Version 2) Case Set
2020-03-30
phs001172 National Institute of Neurological Disorders and Stroke (NINDS) Parkinson's Disease Case-Control
2016-07-19
phs001173 National Cancer Institute (NCI) Head and Neck Cancer Study Case-Control
2016-07-19
phs001174 Female Infertility: Primary Ovarian Insufficiency Case Set
2016-07-20
phs001175 CTSP: Clinical Trial Sequencing Project Case Set
2018-12-13
phs001176 Gene-Environment Interactions (GxE) and Complex Traits Reference Set
2019-08-26
phs001177 Rare germline sequence variants, copy number variations, expression alterations, methylation variations and disease susceptibility in familial melanoma Family
2017-08-01
phs001178 Disorders/Differences of Sex Development (DSD) Study Performed at UCLA in Collaboration with the DSD-Translational Research Network (DSD-TRN), with the Support of the Gabriella Miller Kids First Pediatric Research Program Parent-Offspring Trios
2016-07-26
phs001179 Foundation Medicine Adult Cancer Clinical Dataset (FM-AD) Case Set
2016-07-28
phs001180 Genes-Environments and Admixture in Latino Asthmatics (GALA II) Study Case-Control
2019-12-10
phs001181 Single-Cell DNA and RNA Sequencing over A 29-Year Period of A CLL Patient Demonstrating Evolution of Multiple Cell Clones Case Set
2016-08-02
phs001182 National Institute of Environmental Health (NIEHS) Sciences Study of Somatic Mutation Load in Clones of Single Human Cells Control Set
2020-08-23
phs001185 Genome-Wide Scan for Genetic Variants Associated with Early-Onset Prostate Cancer Case-Control
2016-08-08
phs001187 Epigenomics of Human CD8 T cell Differentiation and Aging Case-Control
2016-08-09
phs001188 The Finland-United States Investigation of NIDDM Genetics (FUSION) Study - Islet Expression and Regulation by RNAseq and ATACseq Control Set
2019-02-26
phs001189 NHLBI TOPMed: Cleveland Clinic Atrial Fibrillation (CCAF) Study Case Set
2021-05-18
phs001191 eMERGE: Northwestern (NUgene) WGS Longitudinal
2016-08-14
phs001192 Thoracic Patient-Derived Xenografts Case Set
2016-08-15
phs001193 National Cancer Institute (NCI) Adding Hispanics to Ongoing GWAS in Colorectal Cancer GWAS
2016-08-15
phs001194 National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Pediatric Cardiac Genetics Consortium (PCGC) Study Parent-Offspring Trios
2019-01-01
phs001195 A Study to Assess the Cardiovascular, Cognitive, and Subjective Effects of Atomoxetine in Combination with Intravenous Methamphetamine Case-Control
2016-08-21
phs001196 NIMH (National Institute of Mental Health) De Novo Mutation Identification in Taiwanese Schizophrenia Trios Case-Control
2016-08-22
phs001197 Neural Systems, Inhibitory Control, and Methamphetamine Dependence Case-Control
2016-08-22
phs001198 Early Methamphetamine Abstinence: fMRI and Brain Function Case-Control
2016-08-22
phs001199 TIGER-LC OncoVar Sequencing Case Set
2016-08-22
phs001200 Neutralizing Antibodies against West Nile Virus Identified Directly from Human B Cells by Single-Cell Analysis and Next Generation Sequencing Case Set
2016-08-25
phs001201 ASsessing and Predicting Infant RSV Effects and Severity (AsPIRES) Study Longitudinal
2018-05-10
phs001202 OncoArray: Oral and Pharynx Cancer Case-Control
2022-08-02
phs001203 Stockholm-Tartu Atherosclerosis Reverse Network Engineering Task (STARNET) Case Set
2023-04-25
phs001205 Region-Specific Neural Stem Cell Lineages Revealed by Single-Cell RNA-Sequences from Human Embryonic Stem Cells Single Cell Analysis
2016-08-31
phs001206 Blepharospasm in a Multiplex African-American Pedigree Multiplex Families
2016-08-31
phs001207 NHLBI TOPMed: African American Sarcoidosis Genetics Resource Affected Sib Pairs
2021-02-01
phs001208 Study on the Genetics of Alcoholism (COGA): Smoke screen and exome sequencing Family
2019-05-20
phs001209 Accurate Immune Repertoire Sequencing Reveals Malaria Infection Driven Antibody Lineage Diversification in Young Children Cohort
2016-09-08
phs001210 National Cancer Institute (NCI) Study of Lung Cancer and Smoking Phenotypes in African-American Cases and Controls Case-Control
2016-09-11
phs001211 NHLBI TOPMed - NHGRI CCDG: Atherosclerosis Risk in Communities (ARIC) Case-Control
2020-10-07
phs001212 NextGen Consortium: Globin Gene Expression in Sickle Cell Genotype-Specific iPS Cells Case Set
2016-09-11
phs001213 Molecular Genetics of Heroin Dependence in China Affected Sib Pairs
2020-02-23
phs001214 DNA and RNA Profiling Using Simultaneous Sequencing (Simul-seq) Case Set
2016-09-14
phs001215 NHLBI TOPMed: San Antonio Family Heart Study (SAFHS) Family
2020-10-07
phs001216 A Genome-Wide Association Study for Post-bronchodilator Lung Function in Children with Asthma Cohort
2016-09-18
phs001217 NHLBI TOPMed: Genetic Epidemiology Network of Salt Sensitivity (GenSalt) Cohort
2020-10-07
phs001218 NHLBI TOPMed: Genetic Study of Atherosclerosis Risk (GeneSTAR) Family
2020-10-07
phs001219 Detection of Genes Predisposing to Hematologic Malignancies Family
2016-09-21
phs001221 ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer Cohort
2016-09-29
phs001222 Centers for Common Disease Genomics (CCDG) - Whole Genome Sequencing in Type 1 Diabetes (T1DGC) Case-Control
2016-10-05
phs001223 Analysis of AR Gene Rearrangements in Prostate Cancer Case Set
2016-10-05
phs001224 Platinum Genomes Control Set
2016-10-06
phs001226 Regulatory Genomics of Human Embryonic Development Control Set
2016-10-11
phs001227 Washington University Coronary Artery Disease Study Case-Control
2016-10-11
phs001228 Gabriella Miller Kids First (GMKF) Pediatric Research Program in Susceptibility to Ewing Sarcoma Based on Germline Risk and Familial History of Cancer Parent-Offspring Trios
2016-10-16
phs001229 Sequencing Lymphoma Single Cell Analysis
2016-10-16
phs001230 Estonian Biobank | Estonian Genome Center, University of Tartu Cohort
2016-10-18
phs001231 The Library of Integrated Network-Based Cellular Signatures (LINCS) - NeuroLINCS Case-Control
2017-05-31
phs001232 Clinical and Genetic Evaluation of Individuals with Undiagnosed Disorders through the Undiagnosed Diseases Network (UDN) Cross-Sectional
2022-07-06
phs001233 Disease Severity in Familial Dysautonomia Case Set
2016-10-20
phs001234 Targeted Sequencing of Primary ER-positive Breast Tumors Treated with 5 Years of Tamoxifen Case Set
2016-10-24
phs001235 Susceptibility to Respiratory Infections Due to Autosomal Recessive IFIH1 Mutations Case-Control
2016-10-27
phs001237 NHLBI TOPMed: Women's Health Initiative (WHI) Longitudinal
2020-10-07
phs001238 Genetic Epidemiology Network of Arteriopathy (GENOA) Sibling Cohort
2018-06-13
phs001239 Integrative Analysis of Lung Adenocarcinoma in EAGLE (Phase 2) Case Set
2016-11-06
phs001241 Clonal Architectures and Driver Mutations in Metastatic Melanomas Case Set
2016-11-07
phs001242 Small Genomic Insertions Form Enhancers that Misregulate Oncogenes Sequencing
2016-11-09
phs001243 Genetic Basis of Breast Cancer Resistance in BRCA1 Mutation Carrier Case Set
2016-11-09
phs001244 Nasopharynx Cancer Whole Exome Sequencing Cohort
2016-11-13
phs001245 Autosomal recessive CD70 deficiency is associated with combined immunodeficiency and EBV viremia Case-Control
2016-11-13
phs001246 Genetic Basis of Isolated Arhinia and Bosma Arhinia Microphthalmia Syndrome Case-Control
2016-11-14
phs001247 GMKF: Kids First Pediatric Research Program on Congenital Cranial Dysinnervation Disorders and Related Birth Defects Cohort
2016-11-14
phs001248 Validation of Gene Array to Predict Bacterial Co-infection In Adults Hospitalized with Viral Lower Respiratory Tract Infections (LRTI) Case Set
2016-11-14
phs001249 Chemosensitive Relapse in Small Cell Lung Cancer Patient-Derived Xenografts Case Set
2016-11-15
phs001250 Sequencing of Coding and Non-coding Regions in Primary Breast Cancers and Patient-matched Controls Cohort
2016-11-16
phs001251 Family-Based Study on Ulcerative Colitis with Whole Exome Sequencing Family
2016-11-16
phs001252 Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE) Case-Control
2016-11-16
phs001253 Pharmacogenetics of Efavirenz Discontinuation for Reported Central Nervous System Symptoms Appears to Differ by Race Case-Control
2016-11-21
phs001255 Molecular Evolution of Cancer Tumor vs. Matched-Normal
2016-12-08
phs001256 Genetic Etiology of Hypoplastic Left Heart Syndrome Case-Control
2017-05-11
phs001257 Loss of IFN-gamma Signaling in Tumor Cells Associates with Primary Resistance to Anti-CTLA-4 Therapy Case Set
2017-03-14
phs001258 Total exRNA Profiles from Plasma, Saliva, and Urine of Healthy Subjects Longitudinal
2019-09-18
phs001259 CCDG CVD: VIRGO - Variation in Recover-Role of Gender on Outcomes of Young Acute Myocardial Infarction (AMI) Patients Observational
2016-12-15
phs001260 Metagenomic Epidemiology of Antibiotic Resistance in Infectious Diarrhea Cohort
2016-12-21
phs001261 Palindromic Amplification of The ERBB2 Oncogene in HER2-Positive Breast Cancer Case Set
2016-12-26
phs001263 Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) - Genome-Wide Association Study Meta-Analysis Case-Control
2016-12-28
phs001264 A super-enhancer associated with CD47 links pro-inflammatory signaling to CD47 upregulation in breast cancer Xenograft
2017-01-02
phs001265 Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) - OncoArray Genotypes Case-Control
2017-01-04
phs001266 Genome-Wide Analysis for Addiction Susceptibility Genes Affected Sib Pairs
2020-02-26
phs001267 CIDR/NICHD Genetic Basis of Recessive Pediatric Brain Diseases - Group 2 Cohort
2017-01-10
phs001270 Investigating Genetics of Human Natural Short Sleepers (IGHNSS) Longitudinal
2017-01-18
phs001271 Pooled Genome-Wide Analysis of Kidney Cancer Risk (KIDRISK) Case-Control
2017-01-22
phs001272 Broad Institute Center for Mendelian Genomics Cohort
2017-01-23
phs001273 Oncoarray Consortium - Lung Cancer Studies Case-Control
2023-08-26
phs001275 Differential Gene Expression in Cryptorchid Testes Case-Control
2017-01-25
phs001276 Single-cell Profiling of an In Vitro Model of Human Interneuron Development Reveals Temporal Dynamics of Cell Type Production and Maturation Single Cell Analysis
2017-01-25
phs001277 NHGRI Genome Integrity of iPSCs Study Case-Control
2017-01-25
phs001278 Longitudinal Study of the Porphyrias Longitudinal
2017-01-29
phs001279 Cross-Sectional Characterization of Idiopathic Bronchiectasis Cross-Sectional
2019-03-31
phs001280 Exome Sequencing of Chordoma Cases Case Set
2017-01-30
phs001281 Establishing Reliability for Quantitative EEG, Transcranial Doppler, Behavioral Outcomes and Optical Coherence Tomography in SWS: The Next Step toward Biomarker Development Observational
2019-02-14
phs001282 Pathogenesis and Immunity in Endemic Burkitt Lymphoma Case Set
2023-02-18
phs001284 National Cancer Institute (NCI) Waldenstrom Macroglobulinemia Genome-wide Association Study Case-Control
2017-02-01
phs001285 Response and Resistance to ER-Directed Therapy in Metastatic Breast Cancer Case Set
2017-02-01
phs001286 The Prostate, Lung, Colon, Ovary Screening Trial (PLCO) Cohort
2022-07-10
phs001287 CPTAC Proteogenomic Study Case Set
2023-06-05
phs001288 Longitudinal Study of Genetic Causes of Intrahepatic Cholestasis Longitudinal
2017-02-05
phs001289 Andersen-Tawil Syndrome: Genotype-phenotype correlation and longitudinal study Longitudinal
2017-02-05
phs001290 CIDR: NCI Genome Wide Predictors of Survival in Colorectal Cancer Clinical Trial
2017-02-05
phs001291 Neoadjuvant Trastuzumab Response in Breast Cancer Case Set
2017-02-05
phs001292 Sleep Abnormalities in Rare Genetic Disorders: Angelman Syndrome, Rett Syndrome, and Prader-Willi Syndrome Case-Control
2019-01-27
phs001293 NHLBI TOPMed: HyperGEN - Genetics of Left Ventricular (LV) Hypertrophy Family
2021-05-23
phs001295 Development and Validation of a Disability Severity Index for Charcot-Marie-Tooth Disease (CMT) Cross-Sectional
2019-04-17
phs001296 Investigation of Brain Nitrogen Metabolism in Partial Ornithine Transcarbamylase Deficiency (OTCD) Using 1H MRS, DTI, and fMRI Observational
2019-04-17
phs001297 Prematurity and Respiratory Outcome Program: Clinical Research Center Study of Functional and Lymphocytic Markers of Respiratory Morbidity in Hyperoxic Preemies Observational
2017-02-13
phs001298 Fine Mapping of Eight Psoriasis Susceptibility Loci Case-Control
2017-02-15
phs001299 Nicotine Addiction Genetics and Correlates Affected Sib Pairs
2020-02-26
phs001300 NABEC: North American Brain Expression Consortium Control Set
2022-10-31
phs001303 Genome-Wide Association Study of Sporadic and Familial Testicular Germ Cell Tumors Case-Control
2017-02-20
phs001304 National Cancer Institute (NCI) Biospecimen Pre-analytical Variables (BPV) Analysis Case Set
2017-02-21
phs001305 A Randomized, Double-Blind, Crossover Study of Sodium Phenylbutyrate (Buphenyl) and Low-Dose Arginine (100 mg/kg/day) Compared to High-Dose Arginine (500 mg/kg/day) Alone on Liver Function, Ureagenesis and Subsequent Nitric Oxide Production in Patients with Argininosuccinic Aciduria (ASA) Interventional
2017-02-23
phs001306 Large Scale Meta-analysis Characterizes Genetic Architecture for Common Psoriasis-associated Variants Case-Control
2017-02-26
phs001307 Inherited Genetic Variation and Predisposition to Testicular Germ Cell Tumor: UPenn Local TGCT Study Case-Control
2017-02-26
phs001309 Multicenter International Cross-Sectional Evaluation of Pulmonary Alveolar Proteinosis (MICEPAP) Trial Clinical Trial
2017-02-26
phs001310 Early Onset and Progression of Primary Ciliary Dyskinesia Lung Disease Prior to 10 Years of Age Observational
2019-04-17
phs001311 Phase II Therapeutic Trial of Mexiletine in Non-Dystrophic Myotonia (IND #77,021) Case Set
2017-02-26
phs001312 National Eye Institute (NEI) Primary Open-Angle African American Glaucoma Genetics (POAAGG) Study Case-Control
2017-02-26
phs001313 Modifier Genes in 21-hydroxylase Deficiency Clinical Trial
2017-02-26
phs001314 Potential Modulatory Role of Osteoprotegerin in Bone Metabolism of Patients with 21-Hydroxylase Deficiency Case-Control
2017-02-26
phs001315 GECCO: Detecting Common and Rare Genetic Loci and GxE Interactions in Colorectal Cancer Case-Control
2017-02-26
phs001316 Therapeutic Trial of Potassium and Acetazolamide in Andersen-Tawil Syndrome Clinical Trial
2017-02-26
phs001317 Long-Term Outcome in Offspring and Mothers of Dexamethasone-Treated Pregnancies at Risk for Classical Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency Clinical Trial
2017-02-27
phs001318 A Phase I/II Study of Revlimid (lenalidomide) in Combination with Vidaza (azacitidine) in Patients with Advanced Myelodysplastic Syndrome (MDS) Case Set
2017-02-28
phs001319 Glioma International Case Control Study (GICC) Case-Control
2017-02-28
phs001320 Investigating Human Placentation and Pregnancy Using First Trimester Chorionic Villi Prospective
2017-03-01
phs001321 Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) - OncoArray Genotypes Cohort
2017-03-01
phs001322 NINDS Inherited Forms of Motor Neuron Disease Study Cohort
2022-01-31
phs001323 Multiple Myeloma Genomic Study (MMGS) Cohort
2021-10-12
phs001325 NextGen Consortium: The iPSCORE (iPSC Collection for Omic Research) Resource for Studying the Impact of Genetic Variation on Molecular and Physiological Phenotypes - Whole Genome Sequence Family
2023-04-19
phs001326 A Retrospective and Cross-Sectional Analysis of Patients Treated for SCID Since January 1, 1968 Longitudinal
2019-04-21
phs001327 Childhood Cancer Survivor Study (CCSS) Cohort
2020-12-02
phs001328 Longitudinal Studies of Brain Structure and Function in MPS Disorders Longitudinal
2017-03-07
phs001329 The Natural History of Mucolipidosis Type IV Longitudinal
2019-01-01
phs001330 Characterizing the Neurobehavioral Phenotype(s) in MPS III (Pilot Study) Longitudinal
2019-11-06
phs001331 Longitudinal Study of Immune Mediated Disorders After Allogenic Hematopoietic Cell Transplantation (HCT) Longitudinal
2019-08-29
phs001332 Natural History of and Genetic Modifiers in Spinocerebellar Ataxias Observational
2019-11-06
phs001333 Natural History and Structural Functional Relationships in Fabry Renal Disease Longitudinal
2019-08-28
phs001336 Extracorporeal Life Support Survival in a Pediatric Hematopoietic Cellular Transplant Recipient with Presumed Graft Versus Host Disease-Related Fulminant Myocarditis Case Set
2017-03-21
phs001337 AACR Project Genomics, Evidence, Neoplasia, Information, Exchange (GENIE) Case Set
2017-03-21
phs001338 A whole-genome sequencing study for evolutionary history of Tibetans and their genetic adaptations to high altitude Population
2017-03-23
phs001339 Developmental Mechanisms of Human Congenital Heart Disease in Subjects with 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome) Case Set
2017-03-23
phs001340 Identification and Targeting of Inflammatory Macrophage-Fibroblast Crosstalk in Rheumatoid Arthritis Case Set
2017-03-26
phs001341 The National Heart, Lung, and Blood Institute (NHLBI)-funded Next Generation Genetic Association Studies (NextGen) Consortium: Phenotyping Lipid traits in iPS derived hepatocytes Study (PhLiPS Study) Cohort
2017-03-27
phs001342 Exome Sequencing of Statin-Induced Myopathy Cases Case-Control
2017-03-29
phs001343 Whole Exome Sequences of Human Embryonic Stem Cell Lines Control Set
2017-03-30
phs001344 GnRH Agonist-Induced Ovarian Suppression and Ovarian Steroids in PMDD and Controls Case-Control
2017-03-30
phs001345 NHLBI TOPMed: Genetic Epidemiology Network of Arteriopathy (GENOA) Cohort
2020-10-07
phs001346 Human Gene Expression Patterns Associated with Experimental P. falciparum Infection Clinical Trial
2017-03-30
phs001347 Impact of Respiratory Virus Infections and Bacterial Microbiome Shifts on Lymphocyte and Respiratory Function in Infants Born Prematurely or Full Term Observational
2019-02-25
phs001348 Biesecker Lab (NHGRI) Whole Genome Medical Sequencing for Gene Discovery Parent-Offspring Trios
2017-09-14
phs001349 Identification of 22 Novel Loci Associated with Susceptibility to Testicular Germ Cell Tumors Case-Control
2019-10-06
phs001350 Pancreatitis after Treatment for Acute Lymphoblastic Leukemia (SJIRB XPD04-123 and XPD05-078) Cohort
2017-04-05
phs001351 Research Study into The Molecular Genetics of Hereditary Neuropathies Case Set
2017-04-05
phs001352 Metagenomics-Guided Pathogen Discovery in Travelers' Diarrhea Cohort
2017-04-05
phs001357 The Genomic Landscape of Tuberous Sclerosis Complex (TSC) Case-Control
2017-04-12
phs001358 RareBliss: Rare Bipolar Loci Identification Through Sequencing Study Case-Control
2017-04-16
phs001359 NHLBI TOPMed: GOLDN Epigenetic Determinants of Lipid Response to Dietary Fat and Fenofibrate Longitudinal
2021-05-23
phs001360 The National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) Consortium for the Longitudinal Evaluation of African-Americans with Early Rheumatoid Arthritis (CLEAR) Case-Control
2017-04-17
phs001361 National Eye Institute (NEI) Genetic Epidemiology of Age-Related Macular Degeneration in the Old Order Amish Family
2018-12-11
phs001362 Linked Read Sequencing of Gastric Cancer Metastases for Complex SV Resolution Case-Control
2017-04-24
phs001363 The Pioneer 100 Wellness Project (P100) Longitudinal
2017-04-24
phs001364 Mapping the Human Connectome - Structure, Function, and Heritability: Healthy Young Adults (Age 22-35 Years) Including Twins and their Non-Twin Siblings Control Set
2017-04-26
phs001365 Germline genome-wide association studies in women receiving neoadjuvant chemotherapy with or without bevacizumab on NSABP B-40 Case-Control
2017-04-27
phs001366 A prospective pilot study of genome-wide exome and transcriptome profiling in patients with small cell lung cancer progressing after first-line therapy Case Set
2017-04-27
phs001367 Add Health: Longitudinal Study of a Nationally Representative Sample of Adolescents in Grades 7-12 in the United States during the 1994-95 School Year, Followed into Adulthood with Five Interviews/Surveys in 1995, 1996, 2001-02, 2008, and 2016-18 Longitudinal
2017-04-27
phs001368 NHLBI TOPMed: Trans-Omics for Precision Medicine (TOPMed) Whole Genome Sequencing Project: Cardiovascular Health Study Longitudinal
2020-10-07
phs001369 Germline hypomorphic CARD11 mutations in severe atopic disease Case-Control
2017-05-08
phs001370 Whole Exome Sequencing of Uveal Melanoma Cohort
2017-05-14
phs001371 TNF-induced dynamic regulation of mRNA stabilome in rheumatoid arthritis fibroblast-like synoviocytes Case Set
2017-05-15
phs001372 Integrated Single-Cell Genetic and Transcriptional Analysis Suggests Novel Drivers of Chronic Lymphocytic Leukemia Case Set
2017-05-18
phs001373 Brain Cell Type-Specific Enhancer-Promoter Connectivity Maps and Disease Risk Association Case Set
2019-07-25
phs001374 VA APOLLO Project - Research for Precision Oncology (RePOP) Longitudinal Cohort
2019-09-12
phs001375 Slim Initiative in Genomic Medicine for the Americas (SIGMA): Mexico City Diabetes Study (MCDS) Case-Control
2021-03-01
phs001376 Autosomal Recessive CD55 Deficiency is Associated with Protein Losing Enteropathy, Thrombosis, and Complement Dysregulation Case-Control
2017-06-04
phs001377 Epigenetics of Cocaine and Nicotine Addiction Case Set
2017-06-07
phs001378 Single-cell RNA-Seq of human lymphoma reveals malignant B cell diversity and patterns of T cell immune checkpoint co-expression Case-Control
2017-06-08
phs001379 A Joint Linkage/Association Strategy to Interrogate AMD Genetic Susceptibility Case-Control
2017-06-11
phs001380 Genomic Studies of Gilles de la Tourette Syndrome Case-Control
2017-06-12
phs001381 Gut Microbiome and Types of Colorectal Polyps Cross-Sectional
2017-06-15
phs001382 Reproductive Health in Men and Women with Vasculitis Clinical Trial
2017-06-15
phs001383 Birth Defects: Moebius Syndrome and Related Congenital Facial Weakness Disorders Case Set
2017-06-15
phs001384 Time Lapse to Cancer-Defining the Transition from Polyp to Cancer Case Set
2017-06-18
phs001385 Evaluation of Ancestry Admixture among Chileans Case-Control
2017-06-18
phs001386 Smoking and the Vaginal Microbiome Case-Control
2018-01-04
phs001387 NHLBI TOPMed: Rare Variants for Hypertension in Taiwan Chinese (THRV) Cohort
2021-05-24
phs001388 Slim Initiative in Genomic Medicine for the Americas (SIGMA): Diabetes in Mexico Study (DMS) Case-Control
2021-03-01
phs001389 University of Texas at Austin (UTA) Histone Modification and Gene Expression Profiling in 9 Primary Glioblastoma Multiforme, 2 Anaplastic Astrocytomas and Two Meningiomas Case Set
2017-06-21
phs001391 OncoArray: Prostate Cancer Case-Control
2017-06-22
phs001392 A Prospective Natural History Study of Diagnosis, Treatment and Outcomes of Children with SCID Disorders Longitudinal
2019-04-16
phs001394 The Hypertension-Insulin Resistance Family Study (HTN-IR) Cohort
2017-06-26
phs001395 NHLBI TOPMed - NHGRI CCDG: Hispanic Community Health Study/Study of Latinos (HCHS/SOL) Cohort
2020-10-07
phs001396 Genetics of Pigmentation in Eastern and Southern African Populations Study Cohort
2017-06-28
phs001397 The Mexican-American Coronary Artery Disease Study (MACAD) Cohort
2017-06-29
phs001398 Center for Common Disease Genomics [CCDG] - Cardiovascular: The Bangladesh Risk of Acute Vascular Events (BRAVE) Study Cohort
2017-06-29
phs001399 Development of Precision Neoadjuvant-Adjuvant Therapies Case Set
2017-06-29
phs001400 Advanced Genomic Techniques in Sequencing of Colorectal Cancer Case-Control
2017-07-04
phs001402 NHLBI TOPMed: Whole Genome Sequencing of Venous Thromboembolism (WGS of VTE) Case Set
2021-06-02
phs001403 Somatic mutation burden and copy-number variation analysis in neurofibromatosis type 1-associated plexiform neurofibromas Case-Control
2017-07-06
phs001404 Molecular Profiling of Gallbladder Cancer (MPOG) Case Set
2017-07-06
phs001405 LCCC1122: Defining the Triple Negative Breast Cancer Kinome Response to GSK1120212 Clinical Trial
2017-07-06
phs001406 National Institute of Mental Health (NIMH) Duke Cognition Cohort Control Set
2017-07-06
phs001407 HNPCC-Sys: Molecular Characterization of Lynch Syndromes Tumor vs. Matched-Normal
2017-07-09
phs001409 Understanding the genetic risk underlying racial disparities in uterine fibroids Case-Control
2017-07-09
phs001410 Kids First: Pediatric Research Project on Adolescent Idiopathic Scoliosis Cohort
2020-12-16
phs001411 Action to Control Cardiovascular Risk in Diabetes (ACCORD) Clinical Trial Cohort
2017-07-13
phs001412 NHLBI TOPMed: Diabetes Heart Study (DHS) African American Coronary Artery Calcification (AA CAC) Cohort
2020-10-07
phs001413 Large Scale Genotyping of Psychiatric Disorders Case-Control
2017-07-17
phs001415 Uncovering the Genetic Architecture of Colorectal Cancer with Focus of Rare and Less Frequent Variants Case-Control
2017-07-20
phs001416 NHLBI TOPMed: MESA and MESA Family AA-CAC Family
2020-08-17
phs001417 Scalable Whole-Exome Sequencing of Cell-Free DNA Reveals High Concordance with Metastatic Tumors Case Set
2021-03-22
phs001418 Interpreting molecular role of DNA variants associated with Crohn's Disease through integrative analysis of open chromatin, epigenome and transcriptome data in diverse and relevant tissues and cells Case-Control
2017-07-30
phs001419 A Natural History Study of CMT1B, CMT2A, CMT4A and CMT4C Longitudinal
2017-07-30
phs001420 Kids First: Genomics of Orofacial Cleft Birth Defects in Latin American Families Parent-Offspring Trios
2017-08-01
phs001421 Whole exome sequencing and methylation profiling of uveal melanoma Cohort
2017-08-02
phs001422 GEnomics and Transcriptomics of Human INsulinoma (GETHIN) Case-Control
2020-12-03
phs001423 Tourette International Collaborative Genetics (TIC Genetics) Study - NJCTS and NIMH Multiplex Families
2021-01-24
phs001424 Genomic Analysis of Pre-Treatment and Autopsy Glioblastoma Specimens Longitudinal
2017-08-03
phs001425 Integrative Analysis of Tumor Biopsies on Sequential CTLA-4 and PD-1 Blockade Reveals Markers of Response and Resistance Case Set
2017-08-07
phs001426 Type 1 Diabetes Genetics Consortium (T1DGC): Case-only RNA-Seq Study Case Set
2017-08-10
phs001427 Resistance to Checkpoint Blockade Therapy Through Inactivation of Antigen Presentation Longitudinal
2021-01-12
phs001428 Genome-Wide Predictors of Treatment-Related Toxicities in SWOG S0221 Trial Clinical Trial
2017-08-13
phs001430 Smith-Lemli-Opitz Syndrome: A Longitudinal Clinical Study of Patients Receiving Cholesterol Supplementation Longitudinal
2020-01-27
phs001431 Whole Exome and Whole Genome Profiling as well Genome-Wide Methylation Profiling from Early to Advanced Chronic Lymphocytic leukemia (CLL), Genome-Wide Methylation Profiling in Monoclonal B Cell Lymphocytosis (MBL) Case Set
2022-02-08
phs001432 A Pilot Study of Rapid Autopsy and Procurement of Tissue in Thoracic Malignancy Cancer Patients to Investigate Tumor Heterogeneity Case Set
2017-08-16
phs001433 Non-coding RNAs Activated by the Wnt/Beta-catenin Signaling Pathway in Hepatoblastoma Case-Control
2017-08-17
phs001434 NHLBI TOPMed: Defining the Time-Dependent Genetic and Transcriptomic Responses to Cardiac Injury Among Patients with Arrhythmias Case Set
2021-06-07
phs001435 NHLBI TOPMed: Australian Familial Atrial Fibrillation Study Case Set
2021-06-07
phs001436 Discovering the Genetic Basis of Human Neuroblastoma: A Gabriella Miller Kids First Pediatric Research Program (Kids First) Project Parent-Offspring Trios
2017-08-20
phs001437 Pediatric Preclinical Testing Consortium (PPTC) Cohort
2017-08-20
phs001438 The Dynamic Landscape of Open Chromatin During Human Cortical Neurogenesis Collection
2017-08-20
phs001439 University of Utah Pelvic Organ Prolapse Disorder Study Case Set
2017-08-20
phs001441 Admixture Mapping of Staphylococcus aureus Bacteremia Case-Control
2017-08-21
phs001442 The Environmental Determinants of Diabetes in the Young Study (TEDDY) Longitudinal
2022-04-07
phs001444 Genomic Variation in Diffuse Large B Cell Lymphomas Case Set
2019-11-03
phs001446 NHLBI TOPMed: Severe Asthma Research Program (SARP) Case Set
2021-06-13
phs001447 Genomic Resistance Patterns to Second Generation Androgen Blockade in Paired Tumor Biopsies of Metastatic Castrate-Resistant Prostate Cancer Cohort
2017-08-29
phs001448 Subtyping Sub-Saharan Esophageal Squamous Cell Carcinoma by Comprehensive Molecular Analysis Cohort
2017-08-31
phs001451 A Phase I Study with a Personalized Neoantigen Cancer Vaccine in Melanoma Clinical Trial
2022-07-04
phs001454 Genomic Regions Associated with Susceptibility to Barrett's Esophagus and Esophageal Adenocarcinoma in African Americans: The Cross BETRNet Admixture Study Case Set
2017-09-10
phs001455 Screening Cases of Isolated Dystonia for Variants in CIZ1 Case Set
2017-09-11
phs001457 Accelerating Medicines Partnership-Rheumatoid Arthritis (AMP-RA/SLE) Case-Control
2017-09-14
phs001458 Deep Sequencing Studies for Cannabis and Stimulant Dependence Family
2017-09-14
phs001459 Accelerating Medicines Partnership-Systemic Lupus Erythematosus (AMP-RA/SLE) Case-Control
2017-09-14
phs001460 Genomic-Enabled Medicine for Recurrent Glioblastoma Case Set
2020-04-22
phs001461 Temporal and Clonal Progression in Pediatric Ependymoma Longitudinal
2017-09-18
phs001463 Differential Transcription Start Site Usage in Brain-related Samples Control Set
2017-09-19
phs001464 Impaired HLA Class I Antigen Processing and Presentation as a Mechanism of Acquired Resistance to Immune Checkpoint Inhibitors in Lung Cancer Cohort
2017-09-24
phs001465 Multiregion Sequencing of Localized Prostate Cancer Case Set
2017-09-25
phs001466 NHLBI TOPMed: Pharmacogenomics of Hydroxyurea in Sickle Cell Disease (PharmHU) Case Set
2021-06-14
phs001467 NHLBI TOPMed: Study of Asthma Phenotypes and Pharmacogenomic Interactions by Race-Ethnicity (SAPPHIRE) Case-Control
2021-07-08
phs001468 NHLBI TOPMed: Recipient Epidemiology and Donor Evaluation Study-III Brazil Sickle Cell Disease Cohort (REDS-BSCDC) Cohort
2021-09-01
phs001469 High response rate to anti PD-1 therapy in desmoplastic melanoma Cohort
2017-10-09
phs001470 Study of Women's Health Across the Nation (SWAN) Repository Longitudinal
2017-10-15
phs001471 National Heart, Lung, and Blood Institute (NHLBI) Heart Healthy Lenoir (HHL) Genomics Study Interventional
2017-10-15
phs001472 NHLBI TOPMed: Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE) Case-Control
2021-07-05
phs001473 Clonal Evolution and Transcriptomic Analysis of Chronic Lymphocytic Leukemia Treated with Ibrutinib Longitudinal
2021-11-08
phs001474 Single Cell RNA-Seq Reveals Malignant and Stromal Programs Associated with Metastasis in Head and Neck Cancer Cohort
2017-10-23
phs001475 Field Studies of Human Immunity to Amebiasis in Bangladesh (NIH Birth Cohort) and Exploration of the Biologic Basis for Underperformance of Oral Polio and Rotavirus Vaccines in Bangladesh (PROVIDE) Longitudinal Cohort
2017-10-24
phs001479 A Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B is Associated with Leukocytosis, Lymphadenopathy, Splenomegaly, Necrotizing Granulomas, Hyper-IgM and Thrombocytopenia Case-Control
2017-10-26
phs001480 Genetics of Chemotherapy Induced Peripheral Neuropathy in N08C1 and N08CB Case-Control
2017-11-01
phs001481 Etiological Investigation of Cancer Susceptibility in Inherited Bone Marrow Failure Syndromes: A Natural History Study Prospective
2017-11-02
phs001482 Evaluating genetic ancestry and self-reported ethnicity in the context of carrier screening Cohort
2017-11-05
phs001483 Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) - germline whole genome sequencing Case Set
2017-11-07
phs001484 Pharmacogenomics of HIV Therapy - Atazanavir Bilirubin-related Side Effects Case-Control
2017-11-07
phs001485 Somatic Mutations and Cell Lineage in the Human Brain Case Set
2022-04-27
phs001486 NCI Cancer Model Development for the Human Cancer Model Initiative (HCMI) Longitudinal Cohort
2019-10-08
phs001487 Center Common Disease Genomics [CCDG] - CVD - TAICHI Observational
2017-11-15
phs001488 Creatine in Huntington's Disease (HD) (CREST-E) Multicenter
2017-11-16
phs001489 Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Epilepsy: Epi25 Consortium Case-Control
2019-08-14
phs001490 Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Follow-Up Study: BioMe Biobank Program Case-Control
2017-11-28
phs001491 Genetics of Disorders Affecting Tooth Structure, Number, Morphology and Eruption Case-Control
2023-04-10
phs001492 Genome-Wide Association Study on Calcific Aortic Valve Stenosis in Quebec (QUEBEC-CAVS) Case-Control
2017-11-29
phs001493 Genomic Predictors of Response to Immune Checkpoint Therapy Cohort
2018-08-06
phs001494 AIDS Linked to the Intravenous Experience (ALIVE) Cohort Longitudinal
2017-11-30
phs001495 DAXX restoration suppresses alternative lengthening of telomeres in ATRX wild-type cells Case Set
2019-01-29
phs001496 A Genomic Approach to Warfarin Dose Prescription in Admixed Caribbean Hispanics Case-Control
2017-12-04
phs001497 UCSF Adult Glioma Study Case-Control
2021-08-19
phs001498 INSIGHT (Intervention Nurses Start Infants Growing on Healthy Trajectories) Cohort Cohort
2019-04-15
phs001499 Transdisciplinary Studies of Genetic Variation in Colorectal Cancer(CORECT): Meta-analysis Case-Control
2017-12-04
phs001500 National Cancer Institute (NCI) Primary Human Melanocyte QTL Study eQTL
2021-04-22
phs001501 Impact of Race and Genetic Factors on Beta Blocker Effectiveness in Heart Failure Longitudinal Cohort
2017-12-06
phs001502 Center for Common Disease Genomics (CCDG)-Cardiovascular: University of Pennsylvania Cohort Case-Control
2017-12-10
phs001503 Women's Interagency HIV Study (WIHS) Prospective
2017-12-11
phs001504 Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Follow-Up Study: Research Studies in Hong Kong Case-Control
2021-03-01
phs001505 Host Genetic Determinants of the Outcome of Staphylococcus Aureus Bacteremia by Whole Exome Sequencing Case-Control
2017-12-11
phs001507 Columbia-Yale-Bilkent Study: Genetics Study of Essential Tremor Multiplex Families
2017-12-14
phs001508 Genetic Analysis of Metopic Nonsyndromic Craniosynostosis Case Set
2017-12-14
phs001511 Progress in Diabetes Genetics in Youth (ProDIGY) Exome Sequencing Study: SEARCH for Diabetes in Youth Case-Control
2017-12-14
phs001512 Gene Expression Signatures Characterized by Longitudinal Stability and Inter-Individual Variability Delineate Baseline Phenotypic Groups with Distinct Responses to Immune Stimulation Methods Development
2017-12-17
phs001513 Mechanisms of Chemotherapy Resistance in T-ALL Cohort
2017-12-17
phs001514 NHLBI TOPMed: Walk-PHaSST Sickle Cell Disease (SCD) Clinical Trial
2021-06-15
phs001515 NHLBI TOPMed: My Life Our Future (MLOF) Research Repository of Patients with Hemophilia A (Factor VIII Deficiency) or Hemophilia B (Factor IX Deficiency) Cross-Sectional
2021-05-10
phs001516 Phenotype Risk Scores Identify Patients with Unrecognized Mendelian Disease Patterns Cohort
2018-01-02
phs001517 Genetics of Human Inherited Retinal Diseases (GHIRD) Case Set
2022-05-17
phs001518 Translational Research Investigating Underlying disparities in acute Myocardial infarction Patients' Health status (TRIUMPH) Longitudinal Cohort
2018-01-08
phs001519 A Phase I Study With a Personalized Neoantigen Cancer Vaccine in Glioblastoma Multiforme Case Set
2018-01-09
phs001521 Immunoprotective mechanisms and microbiota interplay in Salmonella Typhi infection Longitudinal
2018-01-15
phs001522 Germline Parent-Offspring Trios
2018-01-15
phs001523 Multi-Omic Microbiome Study-Pregnancy Initiative (MOMS-PI) Longitudinal
2018-01-16
phs001524 The Genetic Basis of Aggressive Prostate Cancer, The Role of Rare Variation Case Set
2020-03-02
phs001525 Genome and Transcriptome Assembly Reveals SVA-Mediated Aberrant Splicing in X-Linked Dystonia Parkinsonism Cohort
2021-05-01
phs001526 Next generation sequencing of diffuse intrinsic pontine glioma samples to identify recurrent mutations, variations, and expression patterns to define novel therapies Sequencing
2018-01-22
phs001527 Oral Microbiome in Esophageal Adenocarcinoma Case-Control
2018-01-22
phs001528 Gene Expression of Small Cell Carcinoma of the Ovary-Hypercalcemic Type (SCCOHT) Case Set
2022-10-18
phs001529 Single-cell RNA-seq of rheumatoid arthritis synovial tissue using low-cost microfluidic instrumentation Case Set
2018-01-25
phs001531 Whole exome sequencing to discover genetic variation associated with aortopathy in Turner Syndrome Case-Control
2018-01-30
phs001532 Nicotine dependence GWAS meta-analysis across European and African American ancestries Case-Control
2020-04-15
phs001534 Pathways Study Longitudinal
2018-02-04
phs001535 Offspring Sex Impacts DNA Methylation and Gene Expression in Placentae from Women with Diabetes during Pregnancy Nested Case-Control
2018-02-04
phs001538 North American Mitochondrial Disease Consortium Patient Registry and Biorepository Methods Development
2018-02-05
phs001539 Myocardial Applied Genomics Network (MAGNet) Study Case-Control
2022-07-06
phs001541 Anorexia Nervosa Genetics Initiative (ANGI) Case-Control
2018-02-12
phs001542 NHLBI TOPMed: Genetics of Asthma in Latino Americans (GALA) Case Set
2021-09-16
phs001543 NHLBI TOPMed - NHGRI CCDG: AF Biobank LMU in the context of the MED Biobank LMU Case Set
2021-06-16
phs001544 NHLBI TOPMed - NHGRI CCDG: Malmo Preventive Project (MPP) Case Set
2021-06-16
phs001545 NHLBI TOPMed - NHGRI CCDG: Intermountain INSPIRE Registry Case Set
2021-06-23
phs001546 NHLBI TOPMed: Determining the Association of Chromosomal Variants with Non-PV Triggers and Ablation-Outcome in AF (DECAF) Longitudinal
2021-06-23
phs001547 NHLBI TOPMed - NHGRI CCDG: The GENetics in Atrial Fibrillation (GENAF) Study Case Set
2021-06-23
phs001548 TCR Repertoire Sequencing to Evaluate the Diversity of Follicular Helper T Cells in HIV Infected Lymph Nodes Cohort
2021-12-14
phs001549 Genome-wide Association Study and Meta-Analysis of Ewing Sarcoma Case-Control
2018-02-14
phs001550 The Genetic and Transcriptomic Evolution of Melanoma Tumor
2022-06-13
phs001551 Epilepsy Genetics Initiative Parent-Offspring
2018-02-15
phs001552 Type 2 Diabetes Genetic Exploration by Next-generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Follow up Study: Pakistan Genomic Resource (PGR) Case-Control
2018-02-22
phs001553 Development of CMT Peds Scale for Children with CMT Longitudinal
2018-03-04
phs001554 Detection of Colorectal Cancer Susceptibility Loci Using Genome-Wide Sequencing Case-Control
2022-09-08
phs001555 Determination of Cross-Reactive Immunological Material (CRIM) status and longitudinal follow-up of individuals with Pompe disease Longitudinal
2018-03-05
phs001556 BRAIN Cell EncyclOpeDia of Transcribed Elements (BRAINcode) Control Set
2018-03-05
phs001557 Mosaic Chromosomal Aneuploidies Detection in Clinical Samples Case-Control
2018-03-07
phs001559 Contribution of Genetic Polymorphisms to the Abuse Liability of Oxycodone Case Set
2018-03-12
phs001560 Novel Factors for Unexplained Phenotypes of Subclinical Carotid Atherosclerosis Case-Control
2018-03-12
phs001561 WES Elucidation of Pathogenetic Mechanisms for Immune System Disorders and NIAID Pilot of Genetic Incidental Finding Management Case Set
2018-03-12
phs001563 Blood Handling and Leukocyte Isolation Methods Impact the Global Transcriptome of Immune Cells Control Set
2018-03-19
phs001564 Structure and Diversity of Urinary Cell-Free DNA Informative of Host-Pathogen Interactions in Human Urinary Tract Infection Sequencing
2020-01-26
phs001565 Genomic Correlates of Response and Resistance to Immune Checkpoint Blockade in Solid Tumors Case Set
2018-03-25
phs001566 Metaplastic breast cancer in a patient with neurofibromatosis type 1 and somatic loss of heterozygosity Case Set
2018-03-25
phs001568 Genetic Epidemiology of Chronic Lymphocytic Leukemia Case-Control
2018-04-01
phs001570 CALGB 40601: Randomized Phase III Trial of Paclitaxel Combined With Trastuzumab, Lapatinib, or Both As Neoadjuvant Treatment of HER2-Positive Primary Breast Cancer Case Set
2022-06-01
phs001571 Genetic Study of Inflammatory Bowel Disease (IBD) in African Americans Case-Control
2018-04-08
phs001572 Pan-tumor genomic biomarkers for personalization of PD-1 checkpoint blockade based immunotherapy Case Set
2018-04-09
phs001573 Intra-tumor heterogeneity and clonal evolution of papillary renal cell carcinoma Case Set
2018-04-09
phs001575 Assessment of Neurological Deterioration in Subjects with Late Infantile Neuronal Ceroid Lipofuscinosis Longitudinal
2019-11-06
phs001576 Longitudinal Study of Bone and Endocrine Disease in Children with MPS I, II, and VI: A Multicenter Study of the Lysosomal Disease Network Longitudinal
2019-08-28
phs001577 Structural Alterations Driving Castration-Resistant Prostate Cancer Revealed by Linked-Read Genome Sequencing Cohort
2018-04-10
phs001578 The preterm infant microbiome: biological, behavioral and health outcomes at 2 and 4 years of age Longitudinal Cohort
2018-04-11
phs001580 Massachusetts General Hospital (MGH)/Broad Hurthle cell carcinoma whole exome sequencing study Cohort
2018-04-19
phs001581 Genomic Characterization of Head and Neck Squamous Cell Carcinoma Cell Lines Case Set
2018-04-23
phs001584 eMERGE Network Phase III: HRC SNV and 1000 Genomes SV Imputed Array Data of 105,000 Participants Case-Control
2019-12-04
phs001585 Identification of ALS Associated Genes Using Whole Genome Sequencing Case-Control
2022-06-23
phs001586 Rhode Island Child Health Study (RICHS) Cohort
2018-04-26
phs001587 Characterization of Prostate Cancer Organoids Case Set
2023-07-09
phs001588 Relationship between low LDL cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: a US-based cross-sectional observational study using electronic medical records Observational
2018-04-29
phs001589 Breast Cancer Family Registry Early-onset Breast Cancer GWAS Case-Control
2018-04-30
phs001590 National Epidemiologic Survey on Alcohol and Related Conditions-III (NESARC-III) Genotype
2021-02-02
phs001591 Center for Oral Health Research in Appalachia (COHRA) Genomic Studies of Oral Health and Disease Cohort
2018-04-30
phs001592 Center for Common Disease Genomics [CCDG] - Cardiovascular ATVB: Atherosclerosis Thrombosis and Vascular Biology Case-Control
2018-05-02
phs001593 Genome Sequencing of Familial Cholangiocarcinoma for the Identification of Germline Risk Alleles Parent-Offspring Trios
2018-05-07
phs001594 Mucosal Melanoma Targeted Exome Sequencing Study (UCSF) Case Set
2018-05-08
phs001595 Norepinephrine Transporter Blockade as a Pathophysiological Biomarker in Neurogenic Orthostatic Hypotension Longitudinal
2018-05-09
phs001596 Acral melanoma targeted exome sequencing study (UCSF) Case Set
2018-05-14
phs001597 Genomic Analysis of Bevacizumab-induced Hypertension Case-Control
2018-05-16
phs001598 NHLBI TOPMed - NHGRI CCDG: The Johns Hopkins University School of Medicine Atrial Fibrillation Genetics Study Case Set
2022-11-15
phs001599 NHLBI TOPMed: Boston-Brazil Sickle Cell Disease (SCD) Cohort Cohort
2018-05-16
phs001600 NHLBI TOPMed - NHGRI CCDG: Early-onset Atrial Fibrillation in the CATHeterization GENetics (CATHGEN) Cohort Case Set
2021-06-29
phs001601 NHLBI TOPMed - NHGRI CCDG: Penn Medicine BioBank Early Onset Atrial Fibrillation Study Case Set
2021-06-28
phs001602 NHLBI TOPMed: Children's Health Study (CHS) Integrative Genetic Approaches to Gene-Air Pollution Interactions in Asthma (GAP) Case-Control
2021-06-29
phs001603 NHLBI TOPMed: Children's Health Study (CHS) Integrative Genomics and Environmental Research of Asthma (IGERA) Case-Control
2021-06-29
phs001604 NHLBI TOPMed: Children's Health Study (CHS) Effects of Air Pollution on the Development of Obesity in Children (Meta-AIR) Case-Control
2021-06-29
phs001605 NHLBI TOPMed: Chicago Initiative to Raise Asthma Health Equity (CHIRAH) Case Set
2021-07-01
phs001606 NHLBI TOPMed: Early-Onset Atrial Fibrillation in the Estonian Biobank Case Set
2021-07-01
phs001607 NHLBI TOPMed: Pulmonary Fibrosis Whole Genome Sequencing Case Set
2021-07-25
phs001608 NHLBI TOPMed: Outcome Modifying Genes in Sickle Cell Disease (OMG) Case Set
2020-10-07
phs001609 Genetic contributions of lupus nephritis in a multi-ethnic cohort of systemic lupus erythematosus (SLE) Case-Control
2018-05-20
phs001611 Organoid Profiling Identifies Common Responders to Chemotherapy in Pancreatic Cancer Cohort
2018-05-29
phs001612 NHLBI TOPMed: Coronary Artery Risk Development in Young Adults (CARDIA) Longitudinal
2018-05-29
phs001615 Comprehensive Epigenetic Landscape of Rheumatoid Arthritis Fibroblast-Like Synoviocytes Case-Control
2018-06-03
phs001616 eMERGE Network Phase III Clinical Sequencing: eMERGEseq Panel Cohort
2019-12-09
phs001617 Genetic Causes of Growth Disorders Family
2018-06-04
phs001618 A Dormant TIL Phenotype Defines Non-Small Cell Lung Carcinomas Sensitive to Immune Checkpoint Blockers Cohort
2018-06-05
phs001619 Genetic analysis of patients with Inherited Retinal Dystrophies (IRDs) using next generation sequencing to identify the causative variants Case-Control
2020-06-02
phs001620 Genetic Testing to Understand and Address Renal Disease Disparities Longitudinal
2018-06-10
phs001621 Genetic Susceptibility and Biomarkers of Platinum-Related Toxicities Longitudinal
2018-06-10
phs001623 Genomic Analysis of Head and Neck Cancers Case Set
2019-10-23
phs001624 NHLBI TOPMed - NHGRI CCDG: The Vanderbilt University BioVU Atrial Fibrillation Genetics Study Case-Control
2023-07-11
phs001625 Whole Genome Sequencing in Psychotic Major Depression Control Set
2018-06-12
phs001626 Longitudinal Multi'omics of the Human Microbiome in Inflammatory Bowel Disease (IBDMDB) Case-Control
2018-06-13
phs001627 High-throughput single-cell DNA sequencing of acute myeloid leukemia tumors with droplet microfluidics Longitudinal
2018-06-13
phs001628 Clinical Resistance to Crenolanib in Acute Myeloid Leukemia Due to Diverse Molecular Mechanisms Longitudinal
2018-06-13
phs001629 Single Patient BRAF Mutant Brain Tumor, Pre- and Post-dabrafenib WES. Case Set
2018-06-14
phs001630 The Immunogenetics of Measles Immunity - Measles (MMR) vaccination (NIAID/NIH) Cohort
2018-06-15
phs001631 Genetics of Mood Disorders: Aging and Emotion Regulation Brain Circuitry in Bipolar Case-Control
2018-06-17
phs001632 African American Multiple Myeloma GWAS Case Set
2018-06-19
phs001641 Implementation, Adoption, and Utility of Family History in Diverse Care Settings Clinical Trial
2018-06-24
phs001642 Center for Common Disease Genomics [CCDG] - Autoimmune: Inflammatory Bowel Disease (IBD) Exomes and Genomes Case-Control
2021-05-10
phs001643 Genomic and transcriptomic characterization of chordoma Case Set
2018-06-25
phs001644 NHLBI TOPMed - NHGRI CCDG: The BioMe Biobank at Mount Sinai Cohort
2020-10-07
phs001645 Genomic Landscape of Cutaneous Diffuse Large B Cell Lymphoma Case Set
2018-06-25
phs001646 Regulatory Changes in Glioblastoma Brain Tumors and Xenografts Wave 1 Case Set
2018-06-28
phs001647 Varieties of Impulsivity in Opiate and Stimulant Users Case-Control
2021-05-24
phs001648 Genomic Characterization of Metastatic Castration Resistant Prostate Cancer Cohort
2019-09-22
phs001649 Center for Education and Drug Abuse Research (CEDAR) Longitudinal
2018-07-05
phs001650 Genetic and Genomic Stability Across Lymphoblastoid Cell Line Expansions Control Set
2018-07-05
phs001651 Whole Exome Characterization of Squamous Cell Lung Cancers (Lung SQCC) from Appalachian Kentucky (APPKY) Case Set
2018-07-11
phs001653 Systematic Analysis of Coding and Non-coding Elements in Developmental Pathways Implicated in Holoprosencephaly Pathogenesis Parent-Offspring Trios
2018-07-19
phs001654 Aspirin and Inflammation: Mutations, Genes, Pathways and Prevention in Barrett's Esophagus Case-Control
2018-07-19
phs001655 Study of the Human Skin Metagenome Associated with Acne Case-Control
2018-07-22
phs001657 Functional Genomic Landscape of Acute Myeloid Leukemia Longitudinal
2020-08-19
phs001658 Metastatic Adrenocortical Carcinoma Displays Higher Mutation Rate and Tumor Heterogeneity than Primary Tumors Cohort
2018-07-30
phs001659 Bayesian-Based Noninvasive Prenatal Diagnosis of Single-Gene Disorders Parent-Offspring Trios
2018-07-31
phs001660 Prospective Analysis of Genotypes in Adults Undergoing Therapy for Lung Cancer (Paclitaxel Cohort) Case Set
2018-08-01
phs001661 NHLBI TOPMed: Genetic Causes of Complex Pediatric Disorders - Asthma (GCPD-A) Case-Control
2021-07-28
phs001662 NHLBI TOPMed: Lung Tissue Research Consortium (LTRC) Case-Control
2020-10-07
phs001663 Neoantigen Landscape in a Hypermutated Glioblastoma Arising in a Patient with Germline POLE Deficiency Treated with Checkpoint Blockade Immunotherapy Longitudinal
2018-08-07
phs001664 Parkinson's Disease Cognitive Genetics Consortium (PDCGC) Stage I, NeuroX Dataset Case Set
2018-08-09
phs001666 A phase II trial of the aurora kinase A inhibitor alisertib for patients with castration resistant and neuroendocrine prostate cancer: efficacy and biomarker evaluation Case Set
2018-08-12
phs001667 Genomics of Kidney Transplantation Cohort
2018-08-12
phs001672 Veterans Administration (VA) Million Veteran Program (MVP) Summary Results from Omics Studies Cohort
2023-06-29
phs001673 ADAGESIII: Contribution of genotype to glaucoma phenotype in African Americans Case-Control
2018-08-15
phs001674 The Genomic Landscape of Endocrine Resistant Advanced Breast Cancers: Paired Pre- and Post-endocrine Therapy Samples. Case Set
2018-08-22
phs001675 Center for Craniofacial and Dental Genetics: Exome Sequencing of Orofacial Cleft Families Nuclear Families
2018-08-26
phs001676 Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Autism - Simons Simplex Collection (SSC) Family
2018-08-26
phs001677 Adolescent Idiopathic Scoliosis (AIS) 1000 Exomes Study Case Set
2018-08-27
phs001678 High-throughput determination of the antigen specificities of T cell receptors in single cells Single Cell Analysis
2018-08-29
phs001679 TRanscriptomic ANalySis of left ventriCulaR gene Expression (TRANSCRibE) Clinical Cohort
2018-08-30
phs001680 Defining T cell States Associated with Response to Checkpoint Immunotherapy in Melanoma Cohort
2018-09-03
phs001682 NHLBI TOPMed: Pulmonary Hypertension and the Hypoxic Response in SCD (PUSH) Case-Control
2021-07-28
phs001683 Clinical Sequencing Exploratory Research Consortium: Incorporation of Genomic Sequencing into Pediatric Cancer Care Longitudinal
2020-07-05
phs001684 Metatranscriptomic Sequencing of Pulmonary Fluid in Immunocompromised Children Case Set
2018-09-05
phs001685 Prediction of DNA Repair Inhibitor Response in Short Term Patient-Derived Ovarian Cancer Organoids Case Set
2018-09-06
phs001686 IL-17 Signaling in Human iPSC-derived Midbrain Neurons in Parkinson's Disease Case-Control
2018-09-06
phs001687 Using Genomics to Reduce Breast Cancer Disparities in the African Diaspora Case-Control
2018-09-06
phs001688 Microarray Gene Expression Data from Early Skin Biopsies of a Secukinumab Clinical Trial in Psoriasis Randomized Controlled Clinical Trial
2018-09-09
phs001689 Multiethnic Cohort Adiposity Phenotype Study (MEC-APS) Cross-Sectional
2018-09-10
phs001690 Somatic Copy Number Analysis of Endometrial Carcinomas Case Set
2018-09-10
phs001691 Genetic Etiology of Heterotaxy Case Set
2018-09-11
phs001692 Lifestyle, Infertility, Fertility, and Evaluation (LIFE) Study Cohort
2018-09-18
phs001693 Maternal-Fetal Immune Responses in Preterm Labor and Congenital Anomalies Cohort
2018-09-18
phs001694 Cerebrospinal Fluid Analysis of HIV-1 Viral Burden in HIV-1 Infected Subjects: Response to Antiretroviral Therapy Cohort
2018-09-18
phs001695 UCSF Center for Reproductive Health (CRH) Research Bank Cohort
2018-09-18
phs001696 Genomic Studies for Understanding Etiology of Esophageal Adenocarcinoma (EsophagealAdenocarcinoma_Chinese) Case Set
2018-09-19
phs001697 Integrative Analysis of Lung Adenocarcinoma in Never Smokers Case Set
2018-09-19
phs001698 Stanford Center for Urologic Genomics: Genomic Analysis of Benign Prostatic Hyperplasia Case Set
2018-09-19
phs001699 Germline DNA Methylation Associated with Breast Cancer Predisposition Case-Control
2018-09-19
phs001700 Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing Case Set
2018-09-24
phs001701 INdiana GENomics: Implementing an Opportunity for the Under Served (INGENIOUS) Cohort
2018-09-26
phs001702 In Vivo Cytokine eQTL Interactions from a Lupus Clinical Trial Cohort
2018-09-27
phs001703 Impact of Genetic Polymorphisms on Human Immune Cell Gene Expression eQTL
2021-03-04
phs001704 Enhancer Mapping in Chronic Lymphocytic Leukemia Case-Control
2018-09-30
phs001705 National Cancer Institute - Population Structure and Natural Selection in the Epidemiology of Burkitt Lymphoma in East African Children and Minors (EMBLEM) study in Uganda Case-Control
2018-09-30
phs001706 Idiopathic Multicentric Castleman Disease Whole Genome Sequencing Project Cohort
2018-10-03
phs001707 University of Pennsylvania CAR T Cell Responding and Non-responding Patients Cohort
2020-01-26
phs001709 Count Me In (CMI): The Metastatic Breast Cancer (MBC) Project (CMI-MBCproject) Cohort
2018-10-03
phs001710 Transplant Outcomes in Aplastic Anemia (TOAA): GWAS and WES Data Cohort
2018-10-03
phs001711 Single-Cell Genome Sequencing of Gastrointestinal Carcinomas Case Set
2018-10-10
phs001712 VCRC Genetic Repository One Time DNA Protocol Case-Control
2018-10-11
phs001713 LCCC 1108: Development of a Tumor Molecular Analyses Program and Its Use to Support Treatment Decisions (UNCseqTM) Cohort
2018-10-11
phs001714 Gabriella Miller Kids First Pediatric Research Program: An Integrated Clinical and Genomic Analysis of Treatment Failure in Pediatric Osteosarcoma Tumor vs. Matched-Normal
2018-10-14
phs001715 VCRC Imaging Protocol for Magnetic Resonance and Positron Emission Tomography in Large-Vessel Vasculitis (Takayasu's Arteritis): Development as Clinical Trial Outcome Measures Vasculitis Clinical Research Consortium Longitudinal
2018-10-14
phs001717 Genetic Variants Influence on the Placenta Regulatory Landscape Control Set
2018-10-15
phs001718 C9ORF72 Hexanucleotide Repeat Sequence Genotyping Project Cohort
2018-10-16
phs001719 Integrated Personal omics Processing (iPoP) Longitudinal multi-omics profiling of prediabetes Longitudinal Cohort
2018-10-16
phs001720 Genome-wide chromatin accessibility profiling of primary human glomerular and kidney cortex tubular outgrowth cultures Collection
2018-10-18
phs001721 NIDDK IBD Genetics Consortium Repository Immunochip Case-Control
2018-10-22
phs001722 Understanding the Progression of Metastatic Colorectal Cancer Cohort
2018-10-22
phs001723 NIDDK IBD Genetics Consortium Repository Exome Chip Case-Control
2018-10-22
phs001724 Genomics and Modification of Pain: A peripheral component identified using iPSCs with the S241T mutation Parent-Offspring Trios
2018-10-22
phs001725 NHLBI TOPMed - NHGRI CCDG: Groningen Genetics of Atrial Fibrillation (GGAF) Study Cohort
2021-07-28
phs001726 NHLBI TOPMed: Childhood Asthma Management Program (CAMP) Parent-Offspring Trios
2020-10-07
phs001727 NHLBI TOPMed: Pathways to Immunologically Mediated Asthma (PIMA) Cohort
2021-08-10
phs001728 NHLBI TOPMed: Best ADd-on Therapy Giving Effective Response (BADGER) Cohort
2021-08-10
phs001729 NHLBI TOPMed: Characterizing the Response to a Leukotriene Receptor Antagonist and an Inhaled Corticosteroid (CLIC) Cohort
2021-08-10
phs001730 NHLBI TOPMed: Pediatric Asthma Controller Trial (PACT) Cohort
2021-08-10
phs001732 NHLBI TOPMed: TReating Children to Prevent EXacerbations of Asthma (TREXA) Cohort
2021-08-10
phs001733 Molecular Etiology of Early-Onset Dystonia Cohort
2018-10-25
phs001734 Youth Drug Abuse, ADHD and Related Disorders Cohort
2018-10-25
phs001735 NHLBI TOPMed: Pediatric Cardiac Genomics Consortium (PCGC)'s Congenital Heart Disease Biobank Case Set
2021-01-05
phs001736 NCI Expanded Genome-Wide Association Study of Renal Cell Carcinoma Case Set
2022-03-24
phs001737 The epigenetic landscape controlled by p63 in epidermal development Case-Control
2019-07-24
phs001738 Kids First Pediatric Research Study in Familial Predisposition to Hematopoietic Malignancies (SJFAMILY-HM) Cohort
2018-11-05
phs001739 Role of the Cervico-Vaginal Microbiome in Spontaneous Preterm Birth Longitudinal
2018-11-06
phs001740 Center for Common Disease Genomics (CCDG) Neuropsychiatric: Study of Autism Genetics Exploration (SAGE) Cohort
2018-11-12
phs001741 Center for Common Disease Genomics (CCDG) Neuropsychiatric: The Autism Simplex Collection (TASC) Cohort
2018-11-12
phs001742 High-Resolution Clonal Mapping of Multi-Organ Metastasis, and Resistance to Neoadjuvant Chemotherapy, in Triple Negative Breast Cancer Case-Control
2019-03-13
phs001743 Contribution of systemic and somatic factors to clinical response and resistance in urothelial cancer: an exploratory multi-omic analysis Longitudinal Cohort
2018-11-12
phs001744 Genome-Wide Association Study of HCC in Non-Asian USA Population Case-Control
2018-11-12
phs001745 Human Lung Tissue eQTL Study Cohort
2018-11-14
phs001746 A Genomic Atlas of Systemic Interindividual Epigenetic Variation in Humans (GTEx) Reference Set
2021-11-16
phs001747 Caregiving as a Natural Stressor in Studies of the Role of Genes That Affect Serotonin Function in Regulating Risk Factors for Coronary Heart Disease (CAREGIVER) Case-Control
2018-11-26
phs001748 Molecular Genetics of Histiocytic Sarcoma Case Set
2018-11-27
phs001749 Genetics of Congenital Anomalies of the Kidney and Urinary Tract Case-Cohort
2021-04-04
phs001750 Single Cell Analysis of Pulmonary Fibrosis Cohort
2018-11-29
phs001751 Rare Disease Susceptibility Variant Study in Children with Crohn's Disease and Their Parents Using Targeted Gene Sequencing. Case-Control
2018-11-29
phs001752 Genomics and Methylation of Neuroendocrine Prostate Cancer from cfDNA (Cornell/Trento 2019) Cohort
2018-12-11
phs001753 Rapid Evolution of a Skin Lightening Allele in Southern African KhoeSan Cohort
2018-12-12
phs001754 Spit for Science Longitudinal
2021-02-15
phs001758 Identification of Rare Germline Variants in Familial Patients with Non-medullary Thyroid Cancer Case Set
2018-12-17
phs001759 Profiles of Extracellular RNA in Cerebrospinal Fluid and Plasma from Subarachnoid Hemorrhage Patients Case Set
2018-12-19
phs001761 Genomic Characteristics of Myeloproliferative Neoplasms in Patients Exposed to Ionizing Radiation following the Chernobyl Nuclear Accident Case-Control
2018-12-27
phs001765 Whole Exome Sequencing of Parathyroid Cancer Identifies Candidate Driver Mutations and Core Pathways Cohort
2019-01-02
phs001766 Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Genetic Resource Exchange Family
2019-01-03
phs001767 Identifying Novel Small RNA Biomarkers Unique to Patients with Gastric Cancer Case-Control
2019-01-03
phs001768 Longitudinal Assessment of Methylmercury and Gut Microbes During Pregnancy Longitudinal
2019-01-08
phs001769 Safety and Efficacy of Intravenous Norepinephrine for Orthostatic Hypotension Interventional
2019-01-09
phs001770 Assessment of Health-related Quality of Life in Rare Kidney Stones Longitudinal
2019-01-09
phs001771 Genomic Diagnosis and Individualized Therapy of Highly Penetrant Genetic Diabetes Longitudinal
2019-01-15
phs001772 A Genomic Approach to Improved Diagnosis and Treatment of Neuroendocrine Tumors Case Set
2022-05-30
phs001774 University of Washington Center for Mendelian Genomics (UW-CMG): Atrioventricular Septal Defects (AVSD) Study Mixed
2019-01-21
phs001775 Alcohol Dependence: Sequencing from Multiplex Families Case-Control
2019-01-23
phs001776 NCI Laboratory of Translational Genomics (LTG) Human Pancreas QTL study Genotype/Expression
2019-01-23
phs001777 Analysis of the Whole Transcriptomes of Human Testis with Complete Spermatogenesis and of Human Testes with Sertoli Cell-Only Syndrome Case-Control
2019-01-24
phs001778 Myelodysplastic Syndrome (MDS) in Humanized Mice Case Set
2019-01-24
phs001779 Center for Inherited Disease Research (CIDR)-National Institute on Aging (NIA) Whole Exome Analysis of Ehlers-Danlos Syndrome Case-Control
2019-01-28
phs001780 African Demographic History Study Using Illumina 1M Array Data Cohort
2019-01-30
phs001781 Proteogenomic Landscape of Squamous Cell Lung Cancer Cohort
2019-02-03
phs001782 Effect of the Placental Transcriptome on Stunting in a Longitudinal African Cohort Longitudinal
2021-06-13
phs001783 Exome Recapture and Sequencing of Prospectively Characterized Clinical Specimens From Cancer Patients Case Set
2023-05-11
phs001784 Molecular Features of Hepatocellular Carcinoma Associated with 18F-Fluorocholine PET/CT Imaging Phenotype Control Set
2019-02-07
phs001785 Gabriella Miller Kids First Pediatric Research Program for Infantile Hemangiomas Associated with Multi-Organ Structural Birth Defects Cohort
2019-02-10
phs001786 Stand Up 2 Cancer (SU2C) Genomics-Enabled Medicine for Melanoma (GEMM) Trial Case Set
2019-02-10
phs001787 Discovery of Colorectal Cancer Susceptibility Genes in High-Risk Families Case Set
2019-02-19
phs001788 Centers for AIDS Research (CFAR) Network of Integrated Clinical Systems (CNICS) Longitudinal
2019-02-19
phs001790 NIMH Human Middle Temporal Gyrus (MTG) Cell Types RNA Sequencing
2019-03-05
phs001791 A Multimodal Atlas of Human Brain Cell Types RNA Sequencing
2019-03-05
phs001792 Intergenerational Impact of Genetic and Psychological Factors on Blood Pressure (InterGEN Study) Longitudinal Cohort
2019-03-05
phs001793 Pharmacogenomic Interactions in Glioblastoma Cell Line Models Case Set
2019-03-06
phs001794 Beckwith-Wiedemann Syndrome (BWS) miRNA Data Cohort
2019-03-10
phs001795 Genetic Analysis of the Chiari I Malformation Case-Control
2019-03-11
phs001796 Correlates of Human Nerve Repair Longitudinal Cohort
2019-03-12
phs001797 UW TAN Study of Metastatic Urothelial Carcinoma Case Set
2019-03-17
phs001798 A New Reference Panel to Boost African American Genotype Imputation Population Genomics
2021-05-16
phs001799 Genomic landscape of Neutrophilic Leukemias of Ambiguous Diagnosis Cohort
2019-03-19
phs001800 Genomics of Pediatric Renal Medullary Carcinomas Cohort
2020-11-09
phs001802 Genetics of Lymphatic Anomalies from Center of Applied Genomics (CAG) at CHOP Cohort
2020-05-20
phs001803 Identification of Genomic Markers of Cervical Dystonia and Subtypes Cohort
2019-03-27
phs001804 NIDA Genetic Epidemiology of Opioid Dependence in Bulgaria (GEODB) Case Set
2019-03-31
phs001805 Endogenous CD4+ T Cells Recognize Neoantigens in Lung Cancer Patients, including KRAS and ERBB2 (Her2) Driver Mutations Case Set
2019-04-02
phs001806 Kids First: Whole Genome Sequencing of Nonsyndromic Craniosynostosis Cohort
2019-04-02
phs001807 InTEAM Consortium - Alcoholic Hepatitis Case Set
2019-04-04
phs001808 Landscape of Somatic Mutations in B Lymphocytes Across Human Lifespan Cross-Sectional
2019-04-07
phs001809 GSCAN GWAS Meta-analysis of Tobacco and Alcohol use (GSCAN-GWAS) Meta-Analysis
2019-04-09
phs001810 Gene-Environment Interactions in COCCaINE Use Disorder: Collaborative Case-Control Initiative in Cocaine Addiction Cohort
2022-07-27
phs001811 Molecular Determinants of Tumor Behavior in Early Lung Adenocarcinoma Cohort
2019-04-14
phs001812 Genetic and Epigenetic Determinants of Pediatric Obesity-Associated Asthma Case-Control
2019-04-15
phs001813 Integrative Tissue Analysis of Men with Prostate Cancer Case Set
2022-04-20
phs001814 Molecular Genetics of Heterotaxy and Related Congenital Heart Defects Case Set
2019-04-28
phs001815 Minority Health Genomics and Translational Research Bio-Repository Database Case-Control
2019-04-28
phs001816 CRISPR-Mediated ASD Gene Knockout Reduces Neuronal Activity Case-Control
2019-04-28
phs001817 GeneScreen, a Population Based, Targeted Genomic Screening Study Cross-Sectional
2019-04-29
phs001818 Single-Cell Genomic Analysis of Gastrointestinal Cancer Case Set
2020-08-30
phs001819 Whole Genome Sequencing to Discover Familial Myeloma Risk Genes Case Set
2020-10-07
phs001820 The Institute for Genomic Medicine at Nationwide Children's Hospital Pediatric Cancer and Blood Disorder Project Cohort
2022-02-01
phs001823 Molecular Biomarkers Predicting Lung Cancer Response Phenotypes Cohort
2019-05-02
phs001824 RNASeq of Plasmacytoid Dendritic Cells in Head and Neck Squamous Cell Cancer Patients Longitudinal Cohort
2019-05-05
phs001825 Study of 5'UTR Mutations in Prostate Cancer Cohort
2019-05-06
phs001826 Mobile Technology to Identify Mechanisms Linking Genetic Variation and Depression in Intern Health Study (IHS) Longitudinal Cohort
2019-05-09
phs001828 Genetic Studies of Chronic Kidney Disease (CKD) Case Set
2019-05-19
phs001829 Molecular Characterization of Response to Rectal Chemoradiation Case Set
2019-05-19
phs001830 Tumor heterogeneity and acquired drug resistance in FGFR2 fusion-positive cholangiocarcinoma through rapid research autopsy Case Set
2019-05-20
phs001831 Elucidating Transcription Regulation by Epigenetics in Neuroblastoma Cohort
2019-05-22
phs001833 Genetic Model of MS Severity Predicts Future Accumulation of Disability Cohort
2019-05-28
phs001834 Genetics of Fuchs Corneal Dystrophy Case-Control
2019-05-29
phs001835 Whole-Exome Sequencing and Targeted DNA Sequencing of Matched Ocular Melanocytosis and Uveal Melanoma Case Set
2019-05-30
phs001836 A Single Cell Transcriptomic Analysis of Human Neocortical Development Cohort
2019-05-30
phs001837 The Intestinal Bacterial Metagenome in Pediatric Non-Alcoholic Fatty Liver Disease (NAFLD) Case-Control
2019-06-02
phs001839 Deep Sequencing of 3 Cancer Cell Lines on 2 Sequencing Platforms (Illumina HiSeqX and NovaSeq) Case Set
2019-06-03
phs001840 Cross-Species Single-Cell Analysis of Pancreatic Ductal Adenocarcinoma Reveals Antigen-Presenting Cancer-Associated Fibroblasts Cohort
2019-06-05
phs001841 CADD/GADD centers on Antisocial Drug Dependence Family
2019-06-05
phs001842 RNAseq of Sjögren's Syndrome and Healthy Volunteers' Salivary Glands Case-Control
2019-06-05
phs001844 Genome-Wide Association of Type 2 Diabetes in Africans: The AADM Study Case-Control
2019-06-06
phs001845 Transcriptomic Analysis of Human Hematopoietic Progenitors from Healthy Donors and Bone Marrow Failure Patients Case-Control
2019-06-06
phs001846 Gabriella Miller Kids First Pediatric Research Program in Genetics at the Intersection of Childhood Cancer and Birth Defects Cohort
2019-06-10
phs001847 Characterization of Structural Variants in Acute Myeloid Leukemia Patients Cohort
2019-06-10
phs001848 Human PI3Kγ Deficiency with Immunodeficiency and Tissue Immunopathology Parent-Offspring Trios
2019-06-11
phs001849 RNA sequencing, ATACseq, and TCR-seq of Tfh cells and CXCR5- CD4+ T cells in HIV infected lymph nodes Cohort
2019-06-16
phs001850 A Phenotypic and Genomics Approach in a Multi-Ethnic Cohort to Subtype Systemic Lupus Erythematosus Prospective
2019-06-16
phs001851 The MALT1 Locus and Peanut Avoidance in the Risk for Peanut Allergy Cohort
2019-06-20
phs001852 Analysis of the Genetic Basis of Height in Large Jewish Nuclear Families Family
2019-06-20
phs001853 Liquid Biopsy Versus Tissue Biopsy to Assess Acquired Resistance and Tumor Heterogeneity in Gastrointestinal Cancers Longitudinal Cohort
2019-06-20
phs001854 Human Pilocytic Astrocytoma Single Cell RNA Sequencing Case Set
2019-06-24
phs001855 Studies of a Targeted Risk Reduction Intervention through Defined Exercise (STRRIDE) Interventional
2019-06-26
phs001856 Transdisciplinary Studies of Genetic Variation in Colorectal Cancer(CORECT): Axiom GWAS Case-Control
2019-06-27
phs001857 Genetics of Mammographic Density in Ashkenazi Jews Cross-Sectional
2019-06-30
phs001858 Anonymized germline variants of prospectively characterized clinical cancer specimens Case Set
2019-06-30
phs001859 Genomic Characterization CS-MATCH-0007 Arm Z1D Cohort
2019-07-02
phs001860 Genetics and Pathophysiology of Autoinflammatory Disorders Parent-Offspring Trios
2019-07-04
phs001861 Single cell analysis reveals new evolutionary complexity in uveal melanoma Case Set
2019-07-04
phs001862 Michigan Polybrominated Biphenyl (PBB) Exposure Registry Cohort
2019-07-04
phs001863 Randomized Phase II 2 x 2 Factorial Trial of the Addition of Carboplatin +/- Bevacizumab to Neoadjuvant Weekly Paclitaxel Followed by Dose-Dense AC in Hormone Receptor-Poor/HER2-Negative Resectable Breast Cancer Clinical Trial
2019-07-07
phs001864 MAP Kinase-Mutant Hematologic Malignancies and Their Therapeutic Resistance Cohort
2019-07-08
phs001865 Emory University African American Vaginal, Oral, and Gut Microbiome in Pregnancy Cohort Study Cohort
2019-07-08
phs001866 RNA Sequence-Based Analysis Used to Compare Breast Primary and Metastatic Tumor Pairs Cohort
2019-07-11
phs001867 Detection of Somatic Mutations In Vitro Aging Cells Population
2019-07-14
phs001868 Cutaneous Melanoma GWAS Combining Multiple Populations and Risk Phenotypes Case-Control
2019-07-15
phs001869 ADHD Genomic Association Study Case-Control
2019-07-16
phs001870 Genomic Changes in Breast Cancer Among Chinese Women in Hong Kong Case Set
2019-07-24
phs001871 Center for Common Disease Genomics (CCDG) - Cardiovascular: Cleveland Clinic Cohort Case-Control
2019-07-25
phs001872 Genome Sequencing of Large, Multigenerational CEPH/Utah Families Cohort
2019-07-29
phs001874 Nature and Contribution of Noncoding, Regulatory Mutations in Neurodevelopmental Disorders Case-Control
2019-07-30
phs001875 Determinants of Venetoclax Resistance Longitudinal
2019-07-30
phs001876 Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders Case-Control
2019-07-31
phs001877 Genetics of Cutaneous T-Cell Lymphoma Case-Control
2019-07-31
phs001879 Microbiota and Complications in Kidney Transplant Recipients Cohort
2019-08-06
phs001880 Center for Common Disease Genomics (CCDG) - Cardiovascular: Emory Cohort Case-Control
2019-08-11
phs001881 A Large Data Resource of Genomic Copy Number Variation across Neurodevelopmental Disorders Case-Control
2019-08-13
phs001882 OncoArray: Follow-up of Ovarian Cancer Genetic Association and Interaction Studies (FOCI) Case-Control
2019-08-13
phs001883 Whole Exome Sequencing of DNA from Pre-and Post-Chemotherapy Needle Biopsies of Triple Negative and Inflammatory Breast Cancers Enrolled in the S0800 Trial Clinical Trial
2019-08-14
phs001884 The Etiological Bases of Giftedness: Epidemiological Study of Cognitive Ability in Children in Saudi Arabia Cohort
2019-08-14
phs001885 Endometrial Cancer Association Consortium - OncoArray Genotypes Case Set
2019-08-18
phs001886 Deciphering Maternal-Fetal Crosstalk in the Human Placenta During Parturition Using Single-Cell RNA-Sequencing Case-Control
2022-03-02
phs001887 Single-Sperm Genome Sequencing of Sperm Donors Cohort
2019-08-19
phs001888 Genomic Characterization CS-MATCH-0007 Arm H Cohort
2019-08-20
phs001889 Transposable Elements in FTLD-TDP and ALS-TDP Case-Control
2019-08-21
phs001890 Single molecule molecular inversion probe capture developed using the CIViC database Tumor vs. Matched-Normal
2019-08-25
phs001892 miRNA Profiling of Maternal and Non-Maternal Healthy Adult Blood Plasma Using Small RNA-Sequencing Case-Control
2019-08-27
phs001894 Center for Common Disease Genomics (CCDG) Neuropsychiatric: Homozygosity Mapping Consortium for Autism (HMCA) Family
2019-09-03
phs001895 Enrichment of PTPRT and JAK2 mutations in lung cancer from African Americans and evidence for increased GI and HRD in LUSC Case-Control
2019-12-05
phs001896 Etiologic Studies of Macular Degeneration Case-Control
2019-09-09
phs001897 Regulatory and Effector T cells in Oral Immunotherapy for Food Allergy Randomized Controlled Clinical Trial
2022-02-27
phs001898 Invariant patterns of clonal succession determine specific clinical features of Myelodysplastic syndromes (MDS) Case Set
2019-09-12
phs001899 NIAID Centralized Sequencing Program Mixed
2020-09-01
phs001900 Genetic Control of Expression and Splicing in Developing Human Brain Cohort
2019-09-17
phs001901 Center for Common Disease Genomics [CCDG] - Cardiovascular: Genetics of Coronary Heart Disease - Characterizaton of Coronary Prone Pedigrees Case-Control
2019-09-18
phs001902 Whole Exome Sequencing Study of TGFΒ Pathway Genes in HCV Liver Fibrosis Case-Control
2019-09-19
phs001903 dbGaP submission of CORECT OncoArray GWAS data Case-Control
2019-09-22
phs001904 Genomic Characterization CS-MATCH-0007 Arm Y Cohort
2019-09-24
phs001905 CIDR: Molecular Pathological Epidemiology of Colorectal Cancer Case Set
2019-09-25
phs001906 Altered chromosomal topology drives oncogenic programs in gastrointestinal stromal tumors Case Set
2019-09-25
phs001907 CPTAC: Microscaled Proteogenomic Methods for Precision Oncology Cohort
2019-09-26
phs001908 Spatiotemporal Analysis of the Human Cerebellum Control Set
2021-02-22
phs001909 The Vaginal Microbiome in Reproductive Age Women Cross-Sectional
2019-09-30
phs001910 Enhancer signatures stratify and predict outcomes of non-functional pancreatic neuroendocrine tumors Case Set
2019-10-02
phs001911 Identifying novel DNA damage response genes in radiosensitive individuals Case Set
2019-10-02
phs001912 Somatic Genome Dynamics of Barrett's Esophagus Patients with Non-Cancer and Cancer Outcomes Case-Control
2019-10-02
phs001913 Center for Common Disease Genomics (CCDG) - Cardiovascular: eMERGE - Northwestern Cohort Case-Control
2019-10-02
phs001914 Improved Detection and Identification of Microsatellite Instability Features in Colorectal Cancer Case-Control
2019-10-02
phs001916 Pilot Sequencing Study: DNA Hydroxymethylation and Gene Expression in Peripheral Blood Mononuclear Cells in Healthy Human Aging Case-Control
2020-04-01
phs001917 DNA Methylation Markers and Pancreatic Cancer Risk in 3 Cohort Studies (NHS, PHS, HPFS) Nested Case-Control
2019-10-09
phs001918 STAMPEED: Whole Genome Association Analysis of Hematopoietic Cell Transplant (HCT) Outcomes Cohort
2021-09-26
phs001919 PAK4 inhibition improves PD-1 blockade immunotherapy Cohort
2019-10-15
phs001920 Genomic Characterization of Brain Metastases from Lung Cancer Cohort
2019-10-15
phs001921 Primary Prostate Tumor Tissue DNA Methylation Profiles Cohort
2019-10-19
phs001922 Chromosome Errors in Human Eggs and Natural Fertility Case Set
2019-10-22
phs001924 Case Study of Acquired Resistance to FGFR Inhibition in Cholangiocarcinoma using Targeted DNA and RNA Sequencing Case Set
2019-10-24
phs001925 Characterization of Clonal Evolution in Microsatellite Unstable Metastatic Cancers through Multi-Regional Tumor Sequencing Case Set
2019-10-31
phs001927 NHLBI TOPMed: SubPopulations and InteRmediate Outcome Measures In COPD Study (SPIROMICS) Cohort
2019-11-04
phs001928 A Comprehensive Genomic Study of Pediatric Malignancy Cohort
2019-11-06
phs001929 Neurogenetic Investigations of Obsessive-Compulsive Disorder Parent-Offspring Trios
2019-11-07
phs001930 Mechanism of Action of Vitamin E in NAFLD Clinical Trial
2019-11-11
phs001931 Count Me In (CMI): The Angiosarcoma (ASC) Project (CMI-ASCproject) Cohort
2019-11-13
phs001932 RNAseq Transcriptomic Analyses of European Ancestry Samples in MGS Dataset Case-Control
2019-11-13
phs001933 NHLBI TOPMed - NHGRI CCDG: UCSF Atrial Fibrillation Study Case Set
2019-11-18
phs001934 Sexual dimorphism in human immune system aging Cross-Sectional
2019-11-19
phs001935 National Cancer Institute Clinical and Laboratory Analysis of Familial Cancer Case Set
2019-11-20
phs001936 Extent and Significance of Bacterial DNA Integrations in the Human Cancer Genome Case Set
2019-11-20
phs001937 DNA Methylomic Profiling of Preeclampsia Across Pregnancy Longitudinal
2019-11-20
phs001938 Genomic and Genetic Characterization of Prostate Tumors Treated with Neoadjuvant Intense Androgen Deprivation Therapy Case Set
2021-08-31
phs001939 Count Me In (CMI): The Metastatic Prostate Cancer (MPC) Project (CMI-MPCproject) Cohort
2022-03-06
phs001940 Multimodal Genomic Features Predict Outcome of Immune Checkpoint Blockade in Non-small Cell Lung Cancer Cohort
2020-01-29
phs001941 NIDCD Otitis Media Genetic Susceptibility and Middle Ear Microbial Shifts Family
2023-03-13
phs001942 Molecular Genetics of Secondary Histiocytic/Dendritic Sarcoma Case Set
2019-12-01
phs001943 Hereditary Cancer Predisposition Syndromes and Uveal Melanoma Cohort
2019-12-02
phs001945 National Institutes of Health H3Africa African Collaborative Center for Microbiome and Genomics Research (ACCME) Longitudinal
2019-12-08
phs001946 Genetic Evaluation of Autoinflammatory Diseases Cross-Sectional
2019-12-09
phs001947 Whole Transcriptome Sequencing of Resectable Stage III/IV Melanoma Evaluated After Starting Hu14.18-IL2 Predicts Outcome Cohort
2019-12-10
phs001948 Genomic Characterization CS-MATCH-0007 Arm W Cohort
2019-12-10
phs001949 Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants Case-Control
2019-12-12
phs001951 Relapsed Acute Lymphoblastic Leukemia (ALL): Mutational Landscape Longitudinal
2022-01-20
phs001953 Genomic profiling for metastatic uveal melanoma from a phase I study of the protein kinase C inhibitor AEB071 Clinical Trial
2019-12-23
phs001954 International Cancer Proteogenome Consortium (ICPC): proteogenomics of early stage lung adenocarcinoma in Taiwan Case Set
2019-12-23
phs001955 NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III - Red Blood Cell Omics (RBC-Omics) Study Cohort
2019-12-26
phs001956 Single-cell analysis reveals different age-related somatic mutation profiles between stem and differentiated cells in human liver Cross-Sectional
2019-12-26
phs001957 Investigation of Human DNA Replication Timing Variation by Whole Genome Sequencing Cohort
2021-05-12
phs001958 Cell-Type Specific Effects of Genetic Variation on Chromatin Accessibility During Human Neuronal Differentiation Cohort
2020-01-01
phs001959 Nanopore cDNA Sequencing of Chronic Lymphocytic Leukemia Case-Control
2020-01-01
phs001960 Epigenome Wide DNA Methylation Study for Osteoporosis Risk Case-Control
2020-01-06
phs001961 LungMAP: Molecular Atlas of Lung Development - Human Lung Tissue Longitudinal
2022-10-20
phs001962 Genomic Profiling of Peripheral T-cell Lymphoma Cohort
2020-01-12
phs001963 DEMENTIA-SEQ: WGS in Lewy Body Dementia and Frontotemporal Dementia Case-Control
2021-07-06
phs001964 Women's Health Study Accelerometry Dataset Longitudinal
2020-01-13
phs001965 MP2PRT: Identification of Genetic Changes Associated with Relapse and/or Adaptive Resistance in Patients Registered as Favorable Histology Wilms Tumor on AREN03B2 Case Set
2020-01-13
phs001966 L1 Retrotransposon sequencing in Cocaine Use Disorder - Study 1 Case-Control
2020-01-27
phs001967 Molecular Biomarkers in Glioma (Mechanisms and Therapeutic Implications of Hypermutation in Gliomas) Case Set
2020-01-28
phs001968 L1 Retrotransposon Sequencing in Schizophrenia - Study 1 Case-Control
2020-01-28
phs001969 Cellular Origins and Genetic Landscape of Cutaneous GD T Cell Lymphoma Case Set
2020-01-29
phs001970 DNA Methylation Characterization of Fusion-Positive and Fusion-Negative Rhabdomyosarcoma Case Set
2020-01-29
phs001971 Kidney Two-Hit Mapping Case Set
2020-01-30
phs001972 NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III - Brazil Sickle Cell Disease Cohort (REDS-BSCDC) Cohort
2020-01-30
phs001973 Genomic Characterization CS-MATCH-0007 Arm Z1A Cohort
2020-01-30
phs001974 NHLBI TOPMed: Genomic Summary Results for the Trans-Omics for Precision Medicine Program Case Set
2023-02-22
phs001975 SNP array analysis of spondylocostal dysostosis patient iPSCs and gene edited isogenic controls Case-Control
2020-02-04
phs001976 Natural History, Pathogenesis and Outcome of Melorheostosis Longitudinal
2020-03-25
phs001977 Large Cancer Fingerprint Screening for Detection of Minimal Residual Disease. Case-Control
2020-02-09
phs001978 IGNITE: Implementing GeNomics In practice: Genomic Medicine Implementation - The Personalized Medicine Program Clinical Trial
2020-02-12
phs001979 Genomic Landscape of Human Skin at a Single-Cell Resolution Cross-Sectional
2020-02-12
phs001980 University of Texas PDX Development and Trial Center Grant Cohort
2021-12-01
phs001981 National Institute on Alcohol Abuse and Alcoholism (NIAAA) Postmortem Prefrontal Cortex eQTL and mQTL Study Case-Control
2020-02-17
phs001982 Rb and p53-Deficient Myxofibrosarcoma and Undifferentiated Pleomorphic Sarcoma Require Skp2 for Survival Case Set
2020-02-23
phs001983 HTAN Pilot Project: Single-Cell Transcriptomics Toolbox for Fresh and Frozen Human Tumors (Lung, Breast, Ovarian, Melanoma, Neuroblastoma, Sarcoma, Glioblastoma, Glioma, and Leukemia) Case Set
2020-02-25
phs001984 GWAS for Membranous Nephropathy Case-Control
2020-02-26
phs001987 Gabriella Miller Kids First Pediatric Research Program in Enchondromatoses and Related Malignant Tumors Cohort
2022-09-19
phs001988 Molecular Characterization of Prostate Cancer Specimens by Bulk and Single Cell Analysis Randomized Controlled Clinical Trial
2020-03-02
phs001990 Epigenomics of Patient Outcomes after Aneurysmal SAH Longitudinal
2020-03-04
phs001991 dbGaP Collection: NHLBI Heart Failure Related dbGaP Data (No IRB requirement) Collection
2020-03-05
phs001992 A panel of reference haplotypes for imputing complement component 4 (C4) gene structural variation Cohort
2020-03-09
phs001993 Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define pre-malignant neurofibromatosis type 1-associated atypical neurofibromas Cohort
2020-03-10
phs001994 Effects of tobacco smoking on the tumor immune microenvironment in head and neck squamous cell carcinoma Cohort
2020-03-12
phs001995 Capturing the genetic diversity of the Himba population Family
2020-03-16
phs001997 Gabriella Miller Kids First Pediatric Research Program in Whole Genome Sequencing of African and Asian Orofacial Clefts Case-Parent Triads Cohort
2020-03-19
phs001998 Evolutionary Analysis of Chronic Lymphocytic Leukemia Cells During Relapse After Allogeneic Hematopoietic Stem Cell Transplant Case Set
2020-03-22
phs001999 Advanced Genetic and Molecular Analysis of Solid Tumors Case-Control
2020-03-24
phs002000 The Genomic Landscape of Mongolian Hepatocellular Carcinoma Case Set
2020-03-24
phs002001 Clonal Evolution and Heterogeneity of Osimertinib Acquired Resistance Mechanisms in EGFR Mutant Lung Cancer Longitudinal
2020-03-26
phs002002 Landscape of Intratumoral NK Cell and ILC in Head and Neck Squamous Cell Carcinoma Case Set
2020-03-30
phs002003 University of Washington Developmental Single Cell Atlas Control Set
2020-03-31
phs002004 Center for Common Disease Genomics (CCDG)-Neuropsychiatric: A Study of the Genetic Causes of Complex Pediatric Disorders (CAG) Family
2020-04-01
phs002005 MP2PRT: Comprehensive Genomic Profiling to Identify Alterations Associated with Relapse for NCI Standard Risk (SR) B-Lineage ALL and NCI High Risk (HR) B-Lineage ALL with Favorable Genetic Features Case-Control
2020-04-03
phs002006 Segmental Overgrowth/Vascular Anomalies/Dermatologic Disorders Case Set
2020-08-04
phs002007 Transcriptomic Characterization of Human Innate T Cells Control Set
2020-04-06
phs002008 The Epigenomic Atlas of Early Human Craniofacial Development Control Set
2020-04-08
phs002009 Genomic Landscape of Pediatric Germ Cell Tumors Case Set
2020-04-13
phs002010 The Research Institute at Nationwide Children's Hospital Genetics of Congenital Heart Disease (CHD) Case Set
2020-04-13
phs002011 PLCO - Limited Use Pilot Test Data Longitudinal
2020-04-13
phs002012 SEER Remote Access Pilot Test Data (2018) Methods Development
2020-04-13
phs002015 National Eye Institute (NEI) Age-Related Eye Disease Study 2 (AREDS2) Case Set
2021-02-25
phs002016 MicroRNA Biomarkers for Prediction of Preeclampsia Case-Control
2020-04-16
phs002017 Circulating RNA profiles of healthy and preeclamptic pregnancies Case-Control
2020-04-16
phs002018 Center Common Disease Genomics [CCDG] - Cardiovascular: Partners Biobank Case-Control
2020-04-20
phs002019 Whole exome and transcriptome analysis of UV-exposed epidermis and carcinoma in situ reveals early drivers of carcinogenesis Case Set
2020-04-21
phs002020 Clinical and genetic analysis of retinopathy of prematurity - GWAS Longitudinal
2020-04-22
phs002021 Phase II trial of targeted immune-depleting chemotherapy and reduced-intensity allogeneic hematopoietic stem cell transplantation using 8/8 and 7/8 HLA-matched unrelated donors and utilizing two graft-versus-host disease prophylaxis regimens for the treatment of leukemias, lymphomas, and pre-malignant blood disorders Clinical Trial
2020-04-22
phs002022 Genomic analysis of primary plasma cell leukemia reveals complex structural alterations and high risk mutational patterns Cohort
2020-04-22
phs002023 Drug screening of patient-derived organoids from colorectal peritoneal metastases Cohort
2020-04-28
phs002024 DCCT/EDIC Epigenetics (DNA Methylation) Study Cohort
2020-04-29
phs002025 Early progression to active tuberculosis is a highly heritable trait driven by 3q23 in Peruvians Case-Control
2020-05-05
phs002027 Induction of HIV-1 Env-Specific Peripheral Blood Plasmablasts and Clonal Persistence as Bone Marrow Plasma Cells Following Vaccination in Humans Longitudinal
2021-11-23
phs002028 Genomic Characterization CS-MATCH-0007 Arm B Cohort
2020-05-13
phs002029 Genomic Characterization CS-MATCH-0007 Arm R Cohort
2020-05-13
phs002030 Impact of Mobile Element Insertions on Human Transcriptome Variation Reference Set
2020-05-13
phs002031 Decoding Human Heart Morphogenesis through Single-cell Multi-modal Analyses Control Set
2020-05-14
phs002032 Genetic Neuroscience: How Human Genes and Alleles Shape Neuronal Phenotypes Case-Control
2020-05-14
phs002033 A Chromatin Accessibility Atlas of the Developing Human Telencephalon Cohort
2021-11-02
phs002034 Genomic Evolution of Low- and High-Grade Glioma Longitudinal
2020-05-19
phs002035 National Heart, Lung and Blood Institute: Regulation of Motile Cilia Assembly in Lung Disease Case Set
2020-05-25
phs002036 Chromoanasynthesis as a Cause of Jacobsen Syndrome Case Set
2020-05-25
phs002037 Methylation biomarker study of magnesium deficiency and colorectal cancer Randomized
2020-05-25
phs002039 Single-cell analysis of upper airway cells reveals host-viral dynamics in influenza infected adults Cohort
2020-05-26
phs002040 Homozygous IL37 mutation leads to infantile inflammatory bowel disease Parent-Offspring Trios
2020-05-27
phs002041 WGSPD Project 1: Whole Genome Sequencing for Schizophrenia and Bipolar Disorder Case-Control
2020-05-28
phs002042 Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Center of Excellence (ACE II) Family
2020-05-31
phs002043 Center for Common Disease Genomics (CCDG) Neuropsychiatric: Multimodal Developmental Neurogenetics of Females Parent-Offspring Trios
2020-05-31
phs002044 Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Victorian Collaborative AuTism Study (CATS): Family and Community Study of the Genetics of Autism Spectrum Disorder Family
2020-06-03
phs002045 Intraductal transplantation models of human pancreatic ductal adenocarcinoma reveal progressive transition of molecular subtypes Case Set
2020-06-03
phs002046 Grady Trauma Project (GTP) Case-Control
2020-06-04
phs002047 Clinical and Genetic Analysis of Retinopathy of Prematurity (ROP) Case-Control
2020-06-09
phs002048 Mapping Systemic Lupus Erythematosus Heterogeneity at the Single Cell Level Case-Control
2021-03-11
phs002049 Memorial Sloan Kettering (MSKCC) Single Cell Mutational Profiling in Myeloid Malignancies Cohort
2020-06-16
phs002050 OICR: Molecular Pathological Epidemiology of Colorectal Cancer Case Set
2021-03-10
phs002051 DNA methylation in rhabdomyosarcoma PDX and PDX-derived primary cells Case Set
2020-06-22
phs002052 Mitochondrial DNA deletion detection in POLG patients Case-Control
2020-06-23
phs002053 Neoadjuvant Pazopanib in Renal Cell Carcinoma Prospective
2020-06-24
phs002054 Genomic characterization of 9p- syndrome Case Set
2020-06-25
phs002055 Peripheral Blood Transcriptome Analysis of ALS Patients Case Set
2020-06-25
phs002056 Genetic Factors associated with Conversion from Active Surveillance to Treatment for Prostate Cancer Case Set
2020-06-29
phs002057 Systems genetics in human endothelial cells identifies non-coding variants modifying enhancers, expression, and complex disease traits Control Set
2020-06-29
phs002058 Genomic Characterization CS-MATCH-0007 Arm Z1I Cohort
2020-07-01
phs002059 Genes for Non-Syndromic Congenital Heart Disease Case Set
2020-07-05
phs002060 Pharmacogenomic Analysis of Microtubule Targeting Agent Response and Toxicity Cohort
2020-07-08
phs002061 The Surveillance Monitoring for ART Toxicities (SMARTT) and the Women and Infants Transmission Study (WITS) Cohort
2020-07-14
phs002062 Polygenic Risk Score for the Prediction of Breast Cancer Is Related to Lesser Terminal Duct Lobular Unit Involution of the Breast Cross-Sectional
2020-07-14
phs002063 Innate and Adaptive Immunity in Parkinson Disease-P20 Case-Control
2020-07-14
phs002064 Metagenomic Analysis to Identify Novel Infectious Agents in Systemic Anaplastic Large Cell Lymphoma Case-Control
2020-07-14
phs002065 Integrative Somatic and Germline Molecular Characterization of Genitourinary Cancers Case-Control
2020-07-16
phs002066 Mechanisms of Extreme Genomic Instability at Large Transcribed Genes Case-Control
2021-06-09
phs002067 Temporal Lobe Epilepsy and Retrotransposons Case-Control
2020-07-19
phs002068 Sporadic ALS Australia Systems Genomics Consortium (SALSA-SGC) Case-Control
2020-07-19
phs002069 Brain Arteriovenous Malformation Genetics Study Case Set
2020-07-22
phs002070 Genomic Landscape of High-Grade Neuroendocrine Neoplasms Cohort
2020-07-23
phs002071 Multimodal Mapping of the Immune Landscape in Human Pancreatic Cancer Cohort
2020-07-29
phs002073 Effect of Breast Feeding on Immunologic Priming in Young Infants Case-Control
2020-08-03
phs002075 Fetal Chorioamniotic Membranes Show Molecular Changes in Placenta Previa and Placenta Accreta Spectrum Cohort
2020-08-03
phs002083 Role of Tobacco Smoke in Clear Cell Renal Cell Carcinoma Cohort
2020-08-11
phs002088 Drug Signatures for Prediction and Mitigation of Toxicity Control Set
2021-06-03
phs002089 Dynamics of Genomic and Immune Responses During Primary Immunotherapy Resistance in Mismatch Repair Deficient Tumors Case Set
2020-08-12
phs002093 NSIGHT BabySeq Project Case-Control
2020-08-13
phs002094 Newborn Screening Translational Research Network (NBSTRN): Newborn Sequencing in Genomic Medicine and Public Health (NSIGHT2) Clinical Trial
2020-08-13
phs002095 NSIGHT North Carolina Newborn Exome Sequencing for Universal Screening (NC NEXUS) Clinical Trial
2020-08-13
phs002097 Refractory Cancer (RC) Program Case Set
2020-08-13
phs002102 Bone Microarchitecture Cohort
2020-08-13
phs002105 Genomics of Opioid Pharmacogenomics and Acute/Chronic Postsurgical Pain after Major Surgery in Children Longitudinal Cohort
2020-08-13
phs002106 Epigenetic Mechanisms of Inflammation and Fatigue in Head and Neck Cancer Clinical Cohort
2020-08-13
phs002116 Unraveling the Genetic Architecture of Diabetic Retinopathy in South India Case-Control
2020-08-13
phs002120 Center for Sub-Cellular Genomics Single Cell Analysis
2020-08-13
phs002121 Integrated Clinical and Transcriptomic Profiling to Characterize Disease Phenotype Case-Control
2020-08-13
phs002123 Drop-BS: High-Throughput Single-Cell Bisulfite Sequencing on a Microfluidic Droplet Platform Epigenetics
2023-01-05
phs002128 Identification and Molecular Characterization of Somatic Mutations in Malformations of Cortical Development Case Set
2020-08-13
phs002130 Gabriella Miller Kids First Pediatric Research Program in Craniofacial Microsomia Cohort
2020-08-13
phs002139 Environmental Arsenic and Diabetes Mellitus (Chihuahua Cohort) Genotype
2020-08-13
phs002140 Demographically Diverse Substance Use Disorder Cohorts of Dr. Stanley H. Weiss Longitudinal Cohort
2020-08-13
phs002143 Small RNA Sequencing across Diverse Biofluids Identifies Optimal Methods for exRNA Isolation Methods Development
2020-08-13
phs002146 Evolution of Chromatin Architecture and Transcriptional Regulation in Mammals None
2020-08-13
phs002151 Genomic Characterization CS-MATCH-0007 Arm N Cohort
2020-08-13
phs002152 Genomic Characterization CS-MATCH-0007 Arm P Cohort
2020-08-13
phs002153 Genomic Characterization CS-MATCH-0007 Arm S1 Cohort
2020-08-13
phs002156 Molecular Characterization of Hemimegalencephaly Case Set
2020-08-13
phs002161 Kids First: Genomic Analysis of Esophageal Atresia and Tracheoesophageal Fistulas and Associated Congenital Anomalies Cohort
2020-08-13
phs002162 Kids First: Genetics of Kidney and Urinary Tract Malformations Cohort
2021-09-01
phs002164 Translating Gene-Calcium Interactions to Precision Medicine for Colorectal Cancer Case-Control
2020-08-13
phs002170 Genome-Wide Association Study of Patients with Coccidioidomycosis GWAS
2020-08-13
phs002171 Serrated Colorectal Cancer: An Emerging Disease Subtype Case Set
2020-08-13
phs002172 Gabriella Miller Kids First Pediatric Research Project in Microtia in Hispanic Populations Cohort
2020-08-13
phs002173 Gabriella Miller Kids First Pediatric Research Program in Bladder Exstrophy, Epispadias, Complex (BEEC) Cohort
2020-08-13
phs002174 Gabriella Miller Kids First Pediatric Research Project in Cornelia de Lange Syndrome, Related Diagnosis and Structural Birth Defects Cohort
2020-08-13
phs002175 The NCAA-DoD Concussion Assessment, Research, and Education (CARE) Consortium RNA Sequencing
2020-08-13
phs002176 Notch Signaling and Efficacy PD-1/PD-L1 Blockade in Relapsed Small Cell Lung Cancer Clinical Trial
2021-05-06
phs002177 Genomic Characterization CS-MATCH-0007 Arm C1 Cohort
2020-08-13
phs002178 Genomic Characterization CS-MATCH-0007 Arm S2 Cohort
2020-08-13
phs002179 Genomic Characterization CS-MATCH-0007 Arm U Cohort
2020-08-13
phs002180 Genomic Characterization CS-MATCH-0007 Arm Z1B Cohort
2020-08-13
phs002181 Genomic Characterization CS-MATCH-0007 Arm I Cohort
2020-08-13
phs002182 Asthma in the Lives of Families Today (ALOFT) Cohort
2023-04-11
phs002183 The Multiethnic Cohort (MEC) Study None
2020-08-13
phs002184 Transcriptomic Analysis of Pluripotent Stem Cell-Based Model of Human Amniogenesis RNA Sequencing
2020-08-13
phs002185 Genome-Wide Association Study of Genetic Susceptibility for Graft-vs-Host Disease Cohort 1 Cohort
2020-08-13
phs002187 Gabriella Miller Kids First Pediatric Research Program in Germline and Somatic Variants in Myeloid Malignancies in Children Cohort
2020-08-13
phs002188 Single Cell Genomic Analysis of Lymphoma Single Cell Analysis
2022-11-20
phs002189 Merkel Cell Carcinoma Tissue and Data Repository Full Transcriptome Sequencing
2020-08-13
phs002192 Cancer Moonshot Biobank Longitudinal
2020-08-13
phs002193 The Gut Microbiome in Parkinson's Disease Nested Case-Control
2020-08-13
phs002196 Systems Analysis of the PfSPZ Vaccine in Kenyan Infants Interventional
2020-08-13
phs002197 Single Cell and Tissue Level Functional Genomics Analysis of Astrocyte-Related Mechanisms in Taupathy RNA Sequencing
2020-08-13
phs002199 Changes in Oral and Gut Microbiota and Incidence and Severity of Patient-Reported Symptoms in Pre- and Post-Kidney Transplant Patients Cohort
2020-08-13
phs002202 A New High-Throughput Sequencing-Based Technology to Study Heterochromatin Structure Control Set
2020-08-13
phs002203 Longitudinal Study of Fluoride and Other Factors Related to Dental Fluorosis, Dental Caries, and Bone Health Cohort
2020-08-13
phs002204 A Single Cell Atlas of Gene Regulatory Elements in the Human Heart Control Set
2020-08-13
phs002205 Center for Common Disease Genomics [CCDG] - Inflammatory Bowel Disease (IBD) - Global Microbiome Conservancy Host Exomes Longitudinal
2020-08-13
phs002206 Genomic Answers for Kids (GA4K) Case Set
2022-10-31
phs002207 Genomic and Transcriptomic Profiling of Patients with Malignant Pleural and Peritoneal Mesothelioma: The NCI Cohort Case Set
2023-04-02
phs002208 Metatranscriptomic Sequencing of Pre-Transplant Bronchoalveolar Lavage in Pediatric Stem Cell Transplant Patients None
2020-08-13
phs002210 Comprehensive Analysis of Structural Variants in Breast Cancer Genomes Using Single Molecule Sequencing Case Set
2020-08-13
phs002211 Gynecology and Lubricant Effects (GALE) Study Cohort
2020-08-13
phs002212 ZRSR2 Mutant Myelodysplastic Syndromes Case Set
2020-08-13
phs002217 Single Cell ATAC-Seq of MELAS Case Set
2020-08-13
phs002219 Genetic Study of Present-Day Populations of Northern Kenya Cohort
2020-08-13
phs002220 Discovering the Genetic Basis of Cleft Palate: CIDR Parent-Offspring Trios
2020-08-13
phs002221 Genetic Modifiers of Syndromic Orofacial Clefts Whole Genome Sequencing
2020-08-13
phs002222 Transcriptomic and Clonal Characterization of T Cells in the Human Central Nervous System Case-Control
2023-08-26
phs002224 Sputum RNA-Seq from Asthmatic Patients for Microbes and Genes Cross-Sectional
2020-08-17
phs002225 HTAN MCL Pre-Cancer Atlas Pilot Project - Targeted Sequencing Development Study Case Set
2021-09-27
phs002226 Multicenter AIDS Cohort Study (MACS) Cohort
2020-08-18
phs002227 NeuroCHARGE Consortium GWAS of White Matter Hyperintensities on MRI Cohort
2020-08-23
phs002228 Innate Immune Anti-Viral Deaminase Deregulation Fuels Pre-Leukemia Stem Cell Evolution Case-Control
2023-01-08
phs002229 Germ Cell Tumor Molecular Heterogeneity Revealed through Analysis of Primary and Metastasis Pairs Case Set
2020-08-25
phs002230 The UCSD / O'Connor "TSP" (Twin/Sibling/Pedigree) Resource in Hypertension Family
2020-08-27
phs002231 Germ Cell and Associated Heme Malignancies Evolve from a Common Shared Precursor Individual-Level Genomic Data
2020-08-30
phs002232 TOPDECC-Trans-omics for Precision Dentistry and Early Childhood Caries: Genome-Wide Genotyping (CIDR) and Microbiome in the ZOE 2.0 Study Cross-Sectional
2020-08-31
phs002234 Deletion of FUNDC2 and CMC4 on chromosome Xq28 is sufficient to cause hypergonadotropic hypogonadism in men Case-Control
2020-09-01
phs002235 Global Microbiome Conservancy Sequence Data Cross-Sectional
2020-09-01
phs002236 Center for Common Disease Genomics [CCDG] - Cardiovascular: Genetic and Phenotypic Determinants of Blood Pressure and Other Cardiovascular Risk Factors Case-Control
2020-09-01
phs002237 Investigation of MMBIR DNA Repair in Normal and Cancer Human Cells Tumor vs. Matched-Normal
2020-09-02
phs002238 Genomic Profiling of Relapsed and Refractory Childhood Cancers Cohort
2020-09-02
phs002240 Characterization of Sex Differences in Human Placentas Cohort
2020-09-03
phs002242 Center for Common Disease Genomics [CCDG] - Cardiovascular: SWISS-AF/SWISS-AF-PVI/BEAT-AF Cohort
2020-09-07
phs002243 Center for Common Disease Genomics [CCDG] - Cardiovascular: PEGASUS-TIMI 54 Case-Control
2020-09-07
phs002244 A model for predicting response to PD-1 inhibitors in NSCLC Cohort
2020-09-08
phs002245 Genetic Determinants of Susceptibility to Severe COVID-19 Infection Cohort
2020-09-08
phs002249 HuBMAP: KULMAP - Human Kidney, Urinary Tract, and Lung Mapping Center Epigenetics
2022-10-05
phs002250 CIDR: Discovery, Biology, and Risk of Inherited Variants in Glioma Family
2020-09-16
phs002252 Cellular and Molecular Characterization of Renal Cell Carcinoma Cohort
2020-09-17
phs002253 CCG Multicentric Italian Lung Detection (MILD) Case Set
2020-09-17
phs002254 Cystic Fibrosis Nasal Epithelium Gene Expression by RNAseq Cohort
2020-09-20
phs002255 Understanding the Biology of Language Impairment through Whole Genome Sequencing Cohort
2020-09-21
phs002258 Shotgun Transcriptome and Isothermal Profiling of SARS-CoV-2 Infection Reveals Unique Host Responses, Viral Diversification, and Drug Interactions Clinical Diagnostic Testing
2020-09-27
phs002259 Human CD4 Memory T Cell Activation Time Course eQTL
2020-09-28
phs002260 Characterization of Immune Evasion in Merkel Cell Carcinoma Case Set
2023-01-04
phs002262 Characterization of High-Grade Serous Ovarian Cancer Subtypes via Single-Cell Profiling Case Set
2022-11-09
phs002267 HuBMAP: A Spatially Resolved Molecular Atlas of Human Endothelium Epigenetics
2020-10-06
phs002268 HuBMAP: A 3-D Tissue Map of the Human Lymphatic System Control Set
2020-10-06
phs002269 A New Pipeline to Predict and Confirm Tumor Neoantigens Predicts Better Response to Checkpoint Blockade Case Set
2020-10-07
phs002270 Very Low Tumor Mutation Burden Identifies Inflamed Recurrent Glioblastomas Responsive to Cancer Immunotherapy Exome Sequencing
2020-10-07
phs002272 HuBMAP: Single-Cell Data from Human Tissues Collection
2020-10-07
phs002273 Analysis of Recurrently Protected Genomic Regions in Urine Cell-Free DNA Methods Development
2020-10-11
phs002276 Gabriella Miller Kids First Pediatric Research Program in Pediatric T-Cell Acute Lymphoblastic Leukemia Cohort
2021-09-23
phs002279 DNA and RNA sequencing of single human haploid germ cells Case Set
2020-10-25
phs002280 Multimodal Analysis for Human Ex Vivo Studies Shows Extensive Molecular Changes from Delays in Blood Processing Full Transcriptome Sequencing
2020-10-26
phs002282 Center for Common Disease Genomics (CCDG) - Cardiovascular: Harvard Gene-Diet Interaction in a Costa Rican Cohort Whole Genome Sequencing
2020-10-27
phs002283 Selenium Chemoprevention: Benefits and Harms Clinical Trial
2022-02-17
phs002284 Single Cell, Whole Genome Analysis of the Aging Human Cardiomyocytes Single Cell Analysis
2020-10-30
phs002286 A Phase I/II Trial of T Cell Receptor Gene Therapy Targeting HPV-16 E7 for HPV-Associated Cancers Clinical Trial
2020-11-01
phs002287 Evolution of Resistance in ER+ Breast Cancer Case-Control
2020-11-11
phs002288 Analysis of Epigenomes and Genome Topology in Colorectal Cancer Cohort
2020-11-15
phs002289 Yale SPORE in Skin Cancer Project 2 Single Cell Analysis
2020-11-16
phs002290 Tumor Fraction Guided Cell-Free DNA Profiling in Metastatic Cancer Patients Sequencing
2020-11-17
phs002291 Whole Transcriptome Sequencing of Human Tumor Cells and Hematopoietic Stem and Progenitor Cells During Aging and Bone Marrow Disorders Case Set
2020-11-17
phs002292 Functional Enhancer Elements Drive Subclass-Selective Expression From Mouse to Human Neocortex Collection
2020-11-18
phs002294 Evolution of Core Archetypal Phenotypes in High-Grade Serous Ovarian Cancer (HGSOC) Longitudinal
2020-11-19
phs002295 Cross-site Concordance Evaluation of Tumor DNA and RNA Sequencing Platforms of CIMAC-CIDC Network Case Set
2020-11-19
phs002297 The Immune Microenvironment Shapes Transcriptional and Genetic Heterogeneity in Chronic Lymphocytic Leukemia Cohort
2022-04-03
phs002298 Genome-wide association study of skin pigmentation in African Americans Community
2020-11-30
phs002299 PETAL Network: Outcomes Related to COVID-19 Treated With Hydroxychloroquine Among Inpatients With Symptomatic Disease (ORCHID) Trial Clinical Trial
2020-11-30
phs002300 Successful Clinical Response in Pneumonia Therapy (SCRIPT) RNA Sequencing
2020-11-30
phs002301 Whole Genome Sequencing of Skull-Based Chordoma Case Set
2020-12-03
phs002303 PEDS-PLAN - Pediatric Precision Laboratory Advanced Neuroblastoma Therapy Case Set
2020-12-06
phs002304 Germline and Somatic Genetic Landscape of Pediatric Rhabdomyosarcoma Exome Sequencing
2020-12-06
phs002305 Washington University PDX Development and Trial Center Tumor
2020-12-07
phs002307 CSER: South-Seq: DNA Sequencing for Newborn Nurseries in the South Case Set
2020-12-07
phs002308 Characterizing Individual Cells Obtained from Bone Marrow Biopsies of MPN Patients Clinical Cohort
2020-12-08
phs002309 Identification and Characterization of Skin-Resident Memory T cells in Patients with Melanoma-Associated Vitiligo Cohort
2021-07-05
phs002310 International Collaboration of Incident HIV and HCV in Injecting Cohorts (InC3) Longitudinal
2020-12-10
phs002311 GATA2 Deficiency Case Set
2020-12-10
phs002313 Copy-Number Analysis of Understudied Black Women Ovarian Cancers Case Set
2020-12-13
phs002315 Integrated Analysis of Multimodal Single-Cell Data Case Set
2020-12-14
phs002316 Simultaneous Trimodal Single Cell Measurement of Transcripts, Epitopes, and Chromatin Accessibility Using TEA-Seq Epigenetics
2020-12-14
phs002317 Genetic Underpinnings of Ethnic Disparities in Bone Toxicities Between Hispanic and Non-Hispanic Children Treated for Acute Lymphoblastic Leukemia Genotype/Expression array
2020-12-15
phs002319 International Verapamil SR/Trandolapril [INVEST] Genes Study Case-Control
2020-12-17
phs002321 Characterizing Advanced Breast Cancer Heterogeneity and Treatment Resistance through Serial Biopsies and Comprehensive Analytics RNA Sequencing
2020-12-28
phs002322 Kids First: Genetics of Pediatric Germ Cell Tumors Parent-Offspring Trios
2020-12-28
phs002323 Defining and Overcoming Intrinsic T Cell Dysfunction to Enable Pediatric Immunotherapy Case Set
2022-05-22
phs002324 CSER: Genomic Sequencing to Aid Diagnosis in Pediatric and Prenatal Practice: Examining Clinical Utility, Ethical Implications, Payer Coverage, and Data Integration in a Diverse Population Parent-Offspring Trios
2023-02-21
phs002325 Center for Common Disease Genomics (CCDG) - Cardiovascular: BioImage Cohort Case-Control
2021-01-06
phs002327 Therapeutic Targeting of ATR Yields Durable Regressions in High Replication Stress Tumors Clinical Trial
2021-01-10
phs002328 International Genetics of Parkinson Disease Progression (IGPP) Consortium: EPIPARK and HBS2 Cohorts Longitudinal Cohort
2021-01-11
phs002329 Bacterial Vaginosis, Cervical Immune Cells and HIV Susceptibility Cross-Sectional
2021-01-18
phs002330 Kids First and INCLUDE: Down Syndrome, Heart Defects, and Acute Lymphoblastic Leukemia Cohort
2022-02-23
phs002331 Prevention of Viral Hepatitis and HIV in Drug Users - A Hepatitis B Model for HIV and an HB Vaccine Model for HIV Vaccine Trials in Drug Users (DASH) Clinical Trial
2021-01-20
phs002333 Massively Parallel Single-Cell RNA-Sequencing of Chronic Rhinosinusitis Nasal and Sinus Tissue Clinical Cohort
2021-01-25
phs002334 Genetic Determinants of EGFR-Driven Lung Cancer Growth and Therapeutic Response In Vivo Cohort
2021-01-27
phs002335 Dana-Farber Cancer Institute (DFCI) Wu Lab/Avicenne CLL RNA-Seq Study Cohort
2021-01-27
phs002336 NIDDK International IBD Genetics Consortium Repository Global Screening Array Case-Control
2021-01-27
phs002337 CSER: Incorporating Genomics into the Clinical Care of Diverse NYC Children (NYCKidSeq) Clinical Diagnostic Testing
2023-01-10
phs002338 NHLBI TOPMed: Stanford Cardiovascular Institute iPSC Biobank Study (SCVI) Individual-Level Genomic Data
2021-01-31
phs002340 A Multi-Omic Single-Cell Atlas of Human Gynecological Malignancies Case Set
2021-02-02
phs002341 RNA Expression in Diverse Donor Derived Dermal Fibroblasts Correlates with Reprogramming to Pluripotency Cohort
2021-02-03
phs002342 Optimized Polyepitope Neoantigen DNA Vaccines Elicit Neoantigen-Specific Immune Responses in Preclinical Models and in Clinical Translation Individual-Level Genomic Data
2021-02-04
phs002343 Structure of the Mucosal and Stool Microbiome in Lynch Syndrome Case Set
2021-02-04
phs002344 Study of Tumor Recurrence Related to the Expression of the PAX3-FOXO1 Oncogenic Transcription Factor in Fusion-Positive Rhabdomyosarcoma Case Set
2021-02-04
phs002346 Characterization of Immune-Related Gene Expression in Lung Cancer Case Set
2021-02-08
phs002347 PDAC Prognosis Biomarkers in Genomic and Transcriptomic Molecular Data Copy Number Variation (CNV)
2021-02-08
phs002348 Multicenter Study of Hydroxyurea (MSH) Double-Blind
2021-02-09
phs002357 Lineage Plasticity and Immune Cell Heterogeneity Are Coordinately Dysregulated Through Changes in FOXA1 Expression in Bladder Cancers with Squamous Differentiation Exome Sequencing
2021-02-16
phs002361 Genomics and Epigenomics of the Elderly Response to Pneumococcal Vaccines Clinical Cohort
2021-02-21
phs002362 Cooperative Study of Sickle Cell Disease (CSSCD) Case-Control
2021-02-22
phs002363 PETAL Repository of Electronic Data COVID-19 Observational Study (RED CORAL) Case-Cohort
2021-02-24
phs002364 Oral Mucosa Transcriptomic Data from Three HIV+cART Patients Case Set
2021-02-24
phs002365 Derivation and Investigation of The First Human Cell-Based Model of Beckwith-Wiedemann Syndrome Cohort
2021-02-25
phs002366 Lung Cancer Genetic Study Among Asian Never Smokers Case-Control
2023-03-15
phs002367 Longitudinal Study of Vaginal Flora Longitudinal Cohort
2021-03-01
phs002368 CaBagE: a Cas9-Based Background Elimination Strategy for Targeted, Long-Read DNA Sequencing Case Set
2021-03-01
phs002371 Human Tumor Atlas Network (HTAN) Clinical Diagnostic Testing
2023-03-15
phs002372 Novel Approach to High-Throughput Identification and Characterization of Neoantigens Methods Development
2021-03-07
phs002373 Avelumab or M7824 for People with Recurrent Respiratory Papillomatosis Case Set
2021-03-08
phs002377 A Phase I/IB Study of Ipilimumab or Nivolumab in Patients With Relapsed Hematologic Malignancies After Allogeneic Hematopoietic Cell Transplantation Clinical Trial
2021-03-09
phs002380 Characterizing TP53 and PPM1D Mutations as Resistance Drivers to Radiation Therapy in Diffuse Intrinsic Pontine Gliomas Case Set
2021-03-15
phs002383 Treatment of Pulmonary Hypertension and Sickle Cell Disease with Sildenafil Therapy (Walk-PHaSST) Clinical Trial
2021-03-17
phs002385 Hematopoietic Cell Transplant for Sickle Cell Disease (HCT for SCD) Clinical Cohort
2021-03-18
phs002386 Optimizing Primary Stroke Prevention in Children with Sickle Cell Anemia (STOP II) Clinical Trial
2021-03-18
phs002387 Ghana Breast Health Study Case-Control
2021-03-21
phs002388 Genomic and Transcriptomic Markers Associated with Response to Immune Checkpoint Blockade Clinical Cohort
2021-03-21
phs002389 MicroRNAs, Hypertension and End Organ Damage in Humans Case-Control
2021-06-08
phs002391 De Novo Mutation Rates at the Single-Mutation Resolution in the Human Genome Sequencing
2021-03-23
phs002392 Transcriptome of 2-Hydroxypropyl-Beta-Cyclodextrin Treatment in Niemann-Pick Disease Type C1 Clinical Cohort
2021-03-24
phs002393 Precision Medicine for ABCA4 Disease: Modifier Alleles Case Set
2022-01-25
phs002394 Chromatin Accessibility Landscape of Human Pancreatic Ductal Adenocarcinoma (PDAC) Clinical Cohort
2021-03-25
phs002395 Mitochondrial Abnormalities in Schizophrenia and Bipolar Disorder Case-Control
2021-03-31
phs002396 Integrated Metabolic Profiling and Gene Expression Analysis Reveals Therapeutic Modalities in Breast Cancer Tumor vs. Matched-Normal
2021-04-05
phs002398 Genomics of Prostate Cancer Case Set
2021-04-09
phs002400 The Role of Myeloid Cells in Parkinson's Disease Case-Control
2021-04-13
phs002401 High Glucose Macrophage Exosomes Enhance Atherosclerosis by Driving Cellular Proliferation and Hematopoiesis Cohort
2021-04-13
phs002405 Gene Variants in Pheochromocytoma and Paraganglioma Case Set
2021-04-18
phs002406 The Northern Manhattan Family Study - a Sub-Study of the Epidemiologic Study of Stroke Outcome in 3 Ethnic Groups: The Northern Manhattan Study Cohort
2021-04-18
phs002407 A Single Cell Atlas of MMRd and MMRp Colorectal Cancer Case Set
2021-04-21
phs002408 The Role of CTCF in the Organization of the Centromeric 11p15 Imprinted Domain Interactome Case-Control
2021-04-21
phs002410 FHIR Test Study BETA Longitudinal Cohort
2021-04-24
phs002411 Genome Instability in Mammary Cells of Pathogenic BRCA1/2 Mutation Carriers Cross-Sectional
2021-04-25
phs002414 Human Companion Data for 'A Transcriptomic Atlas of Mouse Cerebellar Cortex Reveals Novel Cell Types' Control Set
2021-04-28
phs002415 Hydroxyurea to Prevent Organ Damage in Children with Sickle Cell Anemia (BABY HUG) Phase III Clinical Trial and Follow-Up Observational Studies I and II Clinical Cohort
2021-04-29
phs002416 Characterization of CNS Metastases Case Set
2022-02-15
phs002417 Low Density Genotyping from the Fragile Families and Child Wellbeing Study Longitudinal
2021-05-04
phs002419 Integrative Molecular Characterization of Breast Cancer Case Set
2021-05-05
phs002421 Transcriptomic Profiling of Patient Derived Alternative Lengthening of Telomeres (ALT) and Non-MYCN-Amplified Neuroblastoma Cell Lines Cohort
2021-05-06
phs002422 Experimental PfSPZ Vaccine in Adults Without Malaria Interventional
2021-05-10
phs002423 Study of Controlled Human Malaria Infections to Evaluate Protection After Intravenous or Intramuscular Administration of PfSPZ Vaccine in Malaria-Naive Adults Interventional
2021-05-10
phs002424 Epigenetic Moderators of Naltrexone Efficacy for Alcohol Use Disorder Clinical Trial
2021-05-10
phs002428 Tandem DNA Repeats Activate hTERT Gene Transcription Case-Control
2021-05-13
phs002429 UNC Tumor Donation Program Set 2021 Case Set
2021-05-13
phs002430 Childhood Cancer Data Initiative (CCDI): Genomic Analysis in Pediatric Malignancies Clinical Genetic Testing
2021-05-13
phs002431 Childhood Cancer Data Initiative (CCDI): Enhancement of Data Sharing in Pediatric, Adolescent and Young Adult Cancers Cohort
2021-05-13
phs002432 Wistar PDX Development and Trial Center Case Set
2021-05-17
phs002433 Nasopharyngeal RNASeq Comparing SARS-CoV-2+ Patients and SARS-CoV-2 Negative Control Subjects Collection
2021-05-17
phs002435 Development and Validation of Patient-Derived Xenografts from Fibrolamellar Carcinoma Human Tissue Case Set
2021-05-18
phs002436 Transcriptome and Epigenome of TIL Infusion for Cancer Immunotherapy Case Set
2021-05-19
phs002437 Metformin for Oral Cancer Prevention Case Set
2021-05-20
phs002439 Development and Validation of Organoids from Fibrolamellar Carcinoma Human Cells Case Set
2021-05-21
phs002440 Parallel CRISPR Editing of Familial ALS Mutations Into a Healthy Control iPSC Line Exome Sequencing
2023-07-05
phs002441 High-Throughput and High-Dimensional Single Cell Analysis of Antigen-Specific CD8+ T Cells Cohort
2021-05-24
phs002442 Host Response to Respiratory Infections Collection
2021-05-24
phs002443 Molecular Signatures of DCIS to Invasive Progression for Basal-Like Breast Cancers: An Integrated Mouse Model and Human Tumor Study Cohort
2021-05-25
phs002444 Germline Genetic Variants in Cancer-Susceptibility Genes in Patients with Osteosarcoma Case Set
2021-05-26
phs002445 Resistance to Latent Mycobacterium tuberculosis Infection in Uganda: Immunologic Profiling Case-Control
2023-03-12
phs002446 Single Cell Omics Resolves Transcriptional Alterations in Sjogren's Syndrome Cross-Sectional
2021-05-27
phs002447 Treatment Options for Type 2 Diabetes in Adolescents and Youth (TODAY) Clinical Trial
2021-05-31
phs002448 Inhibition of CDK4/6 Promotes CD8 T Cell Memory Clinical Cohort
2021-05-31
phs002449 Tissue and Fluid Analysis in Ocular Inflammatory Disease Cross-Sectional
2021-06-01
phs002450 Genomic Basis of Phenotypic Variability of Complex Disorders Copy Number Variation (CNV)
2021-06-01
phs002453 Million Veteran Program (MVP) Summary Results from Non-Sensitive Omics Studies Clinical Cohort
2021-06-02
phs002455 Dissecting Autoimmune Cellular and Molecular Networks in Vitiligo Case-Control
2021-06-03
phs002456 Integrated Genomic Analyses of Cutaneous T Cell Lymphomas Reveal the Molecular Bases for Disease Heterogeneity Case Set
2021-06-06
phs002457 Comprehensive Analysis of the Immunogenomics of Triple Negative Breast Cancer Brain Metastases from LCCC1419 Tumor vs. Matched-Normal
2021-06-06
phs002458 Evolution of Chronic Lymphocytic Leukemia to Richter's Syndrome (RS) Longitudinal
2021-06-07
phs002460 Health Professionals Follow-Up Study Longitudinal
2021-06-08
phs002461 Single-Cell Analysis of Human Adipogenesis Full Transcriptome Sequencing
2022-07-06
phs002462 Circulating Tumor Cell Heterogeneity in Neuroendocrine Prostate Cancer by Single Cell Copy Number Analysis Case Set
2021-06-08
phs002463 Natural Genetic Variation in the Human Genome Collection
2021-06-09
phs002464 Leveraging Extended Families for Cardiovascular Disease Genomic Discovery Exome Sequencing
2021-06-10
phs002465 The Human Pancreas Analysis Program (HPAP) Case-Control
2021-06-10
phs002467 Multimodal Profiling of 500,000 Memory T Cells from a Tuberculosis Cohort Identifies Cell State Associations with Demographics, Environment, and Disease Case-Control
2021-06-15
phs002468 Type 1 Diabetes Genetics Consortium (T1DGC): Multi-Ethnic ImmunoChip Study Case-Control
2021-06-16
phs002470 A Polygenic Score for Acute Vaso-Occlusive Pain in Pediatric Sickle Cell Disease Clinical Cohort
2021-06-20
phs002471 Base Editing Reduces Misfolded Protein Accumulation and Toxicity in Alpha-1 Antitrypsin Deficient Patient iPSC-Hepatocytes Collection
2021-06-21
phs002472 Airway Epithelial Cell Culture RNA Expression Cohort
2021-06-21
phs002476 Immune Profiling in Patients with High-Risk Smoldering Myeloma Case-Control
2023-04-18
phs002478 iRHOM2 Deficiency Causes Environmentally Directed Immunodysregulatory Disease Case Set
2021-06-23
phs002479 HCI-PDX Trial Center for Breast Cancer Therapy Case Set
2021-06-23
phs002480 Genomics of Glomerular Disorders Case Set
2023-06-08
phs002481 Gene Expression Study of Individuals with Sex Chromosome Aneuploidies Case-Control
2023-06-08
phs002482 Combined Targeting of CDK4/6 and HER2 Signaling in Orthotopic Patient-Derived Xenografts of HER2-Positive Breast Cancer Brain Metastases Exome Sequencing
2021-06-27
phs002484 Bulk RNA Sequencing of 86 Human Donor Lungs RNA Sequencing
2021-06-30
phs002486 Nivolumab and Tumor Infiltrating Lymphocytes (TIL) in Advanced Non-Small Cell Lung Cancer Clinical Trial
2021-07-01
phs002487 Epigenomes and Transcriptomes of Brain Samples of Schizophrenics and Controls Case-Control
2021-07-01
phs002489 Developmental Dynamics of Translation in the Human Brain Collection
2021-07-04
phs002492 Study of Leukemia Stem Cells in B-ALL Case Set
2021-07-07
phs002493 Genetic Effects on Gene Expression and Splicing during Human Neurogenesis eQTL
2021-07-07
phs002495 Clinical and Genetic Analysis of Costa Rican Patients with Parkinson's Disease Case-Control
2021-07-11
phs002496 Germline Whole-Exome Sequencing of Lung Cancer in EAGLE Case-Control
2021-07-12
phs002498 Integrative Genomic and Transcriptomic Analyses of Refractory Multiple Myeloma Case Set
2021-07-12
phs002499 Primary Cytotoxic T Cell Lymphomas Harbor Recurrent Targetable Alterations in the JAK-STAT Pathway Case Set
2021-07-13
phs002502 Center for Common Disease Genomics [CCDG] Neuropsychiatric: Autism Spectrum Disorder (ASD) – Whole Exomes Parent-Offspring
2023-04-10
phs002503 GWA Study of Oral Cavity, Pharynx and Larynx Cancers in European, and North and South American Populations - CIDR Case-Cohort
2021-07-19
phs002504 UCSF Database for the Advancement of JMML - Integration of Metadata with "Omic" Data Clinical Cohort
2021-07-19
phs002505 CPTAC: Molecular Dissection of Chemotherapy Response in Triple Negative Breast Cancer Case Set
2021-07-20
phs002506 Genome-Wide Approach to Measure Variant-Based Heritability of Drug Outcome Phenotypes Case Set
2021-07-20
phs002507 Developmental Maturation of Hematopoietic Stem and Progenitor Cells Mediated by Lin28b/Let-7/Cbx2 Stem Cell Lines
2021-07-22
phs002508 Human Vaccines Project: scRNAseq Characterization of HepB Vaccine Response Single Cell Analysis
2021-07-25
phs002509 Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Genomics of Autism Spectrum Disorder (GASD) Family
2021-07-25
phs002510 Mechanisms of Restoring T Cell Immunity after Cure of Chronic Viral Infection Epigenetics
2021-07-25
phs002511 Center for Common Disease Genomics [CCDG] - Neuropsychiatric: SPARK Simons Foundation Powering Autism Research for Knowledge Family
2021-07-25
phs002512 Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Simons Searchlight Family
2021-07-25
phs002513 Study of Environment, Lifestyle and Fibroids SNP Data Longitudinal Cohort
2021-07-26
phs002514 Identification of Modifiers of 22q11.2 Deletion Syndrome in Whole Genome Sequence - CIDR Case-Control
2021-07-26
phs002515 Mutational Landscape of MCPyV-Positive and MCPyV-Negative Merkel Cell Carcinomas Case Set
2021-07-26
phs002516 Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): NIH Digital Health Solutions for COVID-19: IBM Covid19 Contact Tracing and Data Exchange Tools Longitudinal
2021-07-26
phs002517 Childhood Cancer Data Initiative (CCDI): Molecular Characterization across Pediatric Brain Tumors and Other Solid and Hematologic Malignancies for Research, Diagnostic, and Precision Medicine Clinical Cohort
2021-07-26
phs002518 Childhood Cancer Data Initiative (CCDI): OncoKids - NGS Panel for Pediatric Malignancies Case Set
2021-07-26
phs002519 Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): Covidseeker and COVID-19 Citizen Science: Leveraging Citizen Science and Real-Time Geospatial Temporal Mobile Data for Digital Contact Tracing and SARS-CoV-2 Hotspotting Case Set
2021-07-26
phs002528 Neuropsychiatric Genetics of African Populations - Psychosis (NeuroGAP-Psychosis) Case-Control
2021-07-27
phs002529 Childhood Cancer Data Initiative (CCDI): Comprehensive Genomic Sequencing of Pediatric Cancer Cases (CMRI/KUCC) Case Set
2021-07-27
phs002533 Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): Digital Health Solutions for COVID-19: COVID Community Action and Research Engagement (COVID-CARE) Cohort
2021-08-01
phs002534 Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): NIH Digital Health Solutions for COVID-19: Team SAE Cohort
2021-08-01
phs002537 Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): COVID-19 Experience Study (C19EX) Survey Longitudinal
2021-08-01
phs002538 Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): ILI Labels and Longitudinal Novel Engagement with Symptom Surveillance (ILLNESS) Study Observational
2021-08-01
phs002539 Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): Large Scale Flu Surveillance Study (LSFS) Longitudinal
2021-08-01
phs002540 Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): NIH Digital Health Solutions for COVID-19: SAFER-COVID - Integration of Testing and Digital Health Longitudinal
2021-08-02
phs002541 Integrated Genomic and Transcriptomic Analysis of Small Cell Lung Cancer Reveals Inter- and Intratumoral Heterogeneity and a Novel Chemotherapy-Refractory Subtype Cross-Sectional
2021-08-03
phs002545 Nivolumab and Ipilimumab and Radiation Therapy in Microsatellite Stable (MSS) and Microsatellite Instable (MSI) High Colorectal and Pancreatic Cancer Case Set
2021-08-04
phs002548 Transcriptome of Chronic Pain and Disease Case-Control
2021-08-08
phs002552 Genomic Analysis of Low Grade B-Cell Lymphoma Case Set
2021-08-09
phs002554 Gene Expression and Epigenetic Analyses of Human Myocytes From Different Muscles Case-Control
2022-01-13
phs002556 Genomic Features of Lung Adenocarcinoma from Individuals with <= 10 Pack-Year Smoking History Case Set
2021-08-12
phs002557 Homozygous Duplication Identified by Whole Genome Sequencing Causes LRBA Deficiency Case Set
2021-08-12
phs002562 Utlizing the RA signature to predict response to TNFi Full Transcriptome Sequencing
2021-08-16
phs002564 Transcriptional Profiling of Macrophages In Situ in Metastatic Melanoma Reveals Localization-Dependent Phenotypes and Function Metastasis
2021-08-17
phs002566 Foregut Microbiome and Risk of Gastric Intestinal Metaplasia, and Gastric Cancer Risk Case-Control
2021-08-20
phs002571 Exome Sequencing for Head and Neck Cancer Susceptibility Sequencing
2021-08-23
phs002576 Longitudinal Immune Dynamics of Mild COVID-19 Define Signatures of Recovery and Persistence Single Cell Analysis
2021-08-26
phs002579 Immune Response to Life-Threatening Respiratory Infections in Children and Young Adults Cross-Sectional
2021-08-26
phs002587 Preclinical Modeling of Leiomyosarcoma Identifies Susceptibility to Transcriptional CDK Inhibitors through Antagonism of E2F-Driven Oncogenic Gene Expression RNA Sequencing
2021-09-01
phs002589 Kids First: Congenital Heart Defects and Laterality Birth Defects Cohort
2021-09-02
phs002590 Kids First: Whole Genome Sequencing in Recessive Structural Brain Defects Parent-Offspring Trios
2021-09-02
phs002591 Kids First: Whole Genome Sequencing in Structural Defects of the Neural Tube Parent-Offspring Trios
2021-09-02
phs002592 Kids First: Genomic Etiologies of CHARGE Syndrome, Related Conditions and Structural Anomalies Cohort
2021-09-02
phs002594 Kids First: Genetic Basis of Fetal Alcohol Spectrum Disorders Cohort
2021-09-02
phs002595 Kids First: Genomics of Orofacial Clefts in the Philippines Cohort
2021-09-02
phs002597 DNA Replication Timing Alterations in Genetic Diseases Aggregate Genomic Data
2022-06-06
phs002598 Inherited Defect in ST6GalNAc1 Reveals Roles of Sialylation in Intestinal Homeostasis Exome Sequencing
2021-09-06
phs002599 NCI CCSG CCDI Supplement Additional Genomic Submission Case Set
2021-09-06
phs002607 Modeling Malignant Progression in Glioma Case Set
2021-09-08
phs002610 Maintenance of Genome Sequence Integrity in Long- and Short-lived Rodent Species Single Cell Analysis
2023-02-01
phs002612 Immunogenomics of Malignant Brain Tumors Exome Sequencing
2021-09-15
phs002613 Characterizing Disease-Causing Variants Using Personal Genomes with Large Recurrent Deletions Clinical Genetic Testing
2021-09-15
phs002614 Multi-Omic Investigation of Beckwith-Wiedemann Syndrome Hepatoblastoma Epigenetics
2021-09-19
phs002615 Somatic Mutations in Epilepsy: Whole Genome Sequence Analysis of Single Neurons Case Set
2021-09-19
phs002620 Feasibility and Clinical Utility of Whole Genome Profiling in Pediatric and Young Adult Cancers Case Set
2021-09-23
phs002621 CIDR: NINDS High Throughput Genotyping Resource Access for Structural Hindbrain Disorders Case-Control
2021-09-23
phs002622 Aurora US Metastatic Breast Cancer Retrospective Project Case Set
2021-09-27
phs002623 Whole Genome Sequencing of Bilateral Cleft Lip and Palate Families from Africa: CIDR Parent-Offspring
2021-09-27
phs002624 Clonal Lineage Tracing of Primary Human Cortical Progenitors, Cell Type Profiles in the Brain Vasculature and Genotyping Data for 22q11DS and Control iPS Lines Cohort
2021-12-28
phs002625 The Spatio-Temporal Evolution of Multiple Myeloma from Baseline to Relapse-Refractory States Exome Sequencing
2021-10-03
phs002627 Kids First: The Genomic Basis of Structural Birth Defects Associated with Chromosome 18 Copy Number Changes Cohort
2021-10-03
phs002628 Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): NIH Digital Health Solutions for COVID-19: Clear2Go - A Digital Identity Wallet for Health Status Clinical Trial
2021-10-03
phs002632 Whole Exome Sequencing in Alopecia Areata Identifies Rare Mutations in KRT82 Case Set
2021-10-04
phs002635 Myelofibrosis Etiology and Transplant Outcomes Case Set
2021-10-05
phs002637 CIDR: The Role of Rare Coding Variation in Prostate Cancer in Men of African Ancestry - RESPOND Project 2 Case-Control
2021-10-05
phs002639 Genomic Analysis of Metastatic Brain Cancer RNA Sequencing
2021-10-12
phs002641 Precision Medicine for Dilated Cardiomyopathy in European and African Ancestry Case Set
2021-10-14
phs002652 Identification of Somatic Changes in Tumors from Fanconi Anemia Patients Copy Number Variation (CNV)
2021-10-17
phs002653 Tumor Mutation Burden, Expressed Neoantigen and Immune Microenvironment in Diffuse Gliomas Aggregate Genomic Data
2021-10-18
phs002654 Genetic Study of Northern Kenya Pastoral Populations Cohort
2021-10-18
phs002659 Genomics from LCCC1525: A Priming Dose of Cyclophosphamide Prior to Pembrolizumab to Treat mTNBC Case Set
2021-10-20
phs002677 Childhood Cancer Data Initiative (CCDI): Integrating Longitudinal Clinical, Sociodemographic and Genomic Data into the NCCR Longitudinal Cohort
2021-10-25
phs002678 Microbiome-Host Interactions in Oral Squamous Cell Carcinoma: a Metatranscriptomic Exploratory Study RNA Sequencing
2021-10-26
phs002681 Natural Killer Cell Therapies for Hematologic Malignancies Clinical Trial
2021-10-28
phs002683 Combined Tumor and Immune Signals From Genomes or Transcriptomes Predict Outcomes of Checkpoint Inhibition in Melanoma Case Set
2021-10-28
phs002684 Single Suture Craniosynostosis: Gene and Pathway Discovery Case Set
2021-10-28
phs002686 Immunophenotyping in a COVID-19 Cohort (IMPACC) Transcriptomics and Genotyping Assays Clinical Cohort
2021-10-31
phs002687 RNA-Seq of Whole Blood from Pediatric Sickle Cell Anemia (SCA) Patients Case-Control
2021-11-03
phs002688 CIDR Estrogen Receptor Negative Breast Cancer in African American Women: DNA Methylation, Reproductive Events, and Mammary Epithelial Cell Populations Case Set
2021-11-04
phs002691 The MD Anderson Colorectal Cancer Case Control Study Case-Control
2021-11-08
phs002692 Pulmonary Fibrosis and Telomerase Dysfunction Case Set
2021-11-09
phs002694 COVID-19 ACTIV-4 ACUTE: A Multicenter, Adaptive, Randomized Controlled Platform Trial of the Safety and Efficacy of Antithrombotic Strategies in Hospitalized Adults with COVID-19 (ACTIV4A) Clinical Trial
2023-02-20
phs002695 Development of Computational Approaches for Cell Hashing in scRNA-Seq Sequencing
2021-11-16
phs002697 A Multimodal Atlas of Human Brain Cell Types 2021 Data Transcriptome Sequencing
2021-11-16
phs002698 Identification of Structural Variants Relevant to Autism by Pacific Biosciences HiFi Whole-Genome Sequencing Affected Sib Pairs
2021-11-17
phs002701 The Role of ZEB2 during Human Neural Crest Cell Formation RNA Sequencing
2021-11-17
phs002703 SEARCH for Diabetes in Youth Study - Genetic Risk Score Case-Cohort
2021-11-18
phs002705 Single Cell Analysis Reveals Immune Dysfunction from the Earliest Stages of CLL that can be Reversed by Ibrutinib Observational
2021-11-21
phs002706 Transformation of Dysplasia in Barrett's Esophagus Case Set
2021-11-21
phs002710 COVID-19 Outpatient Thrombosis Prevention Trial (ACTIV-4B) Clinical Trial
2021-11-22
phs002714 The National Myelodysplastic Syndromes (MDS) Study Clinical Trial
2021-11-22
phs002715 National Sleep Research Resource (NSRR): Cleveland Family Study (CFS) Longitudinal Cohort
2021-11-23
phs002716 Genetics of Hypertension Associated Treatment (GenHAT) Study, Genomic Background of Blood Pressure Response to Treatment in African Americans Clinical Trial
2021-11-29
phs002717 Study of Cutaneous Biology of Cutaneous T Cell Lymphoma Case-Cohort
2021-12-01
phs002718 Genetics of Prostate Cancer in Africa Case-Control
2021-12-01
phs002719 Reasons for Geographic and Racial Differences in Stroke Cardiorenal GWAS GWAS
2021-12-02
phs002723 Discovery and Characterization of Genetic Risk Loci in Sjogren's Syndrome Case-Control
2021-12-05
phs002724 (Epi)genetic Risk Architectures of Opioid-Dependent Brain Case-Control
2021-12-06
phs002725 Novel Gene-Environment Regulatory Circuit in Chamber-Specific Growth of Perinatal Heart Exome Sequencing
2021-12-07
phs002726 Center for Common Disease Genomics [CCDG] - Cardiovascular: Cardiology Biobanking for Biomarker Discovery Case Set
2021-12-07
phs002728 RNA-Seq of PBMC's from rUTI Patients and Healthy Controls Cohort
2021-12-08
phs002731 Multi-Omic Analysis of Von Willebrand Factor Regulation in Endothelial Colony Forming Cells Case-Control
2021-12-12
phs002732 NIH Division of Intramural Research Multiomic Monogenic Disease Study Clinical Cohort
2021-12-13
phs002733 Colon Cancer Family Registry (Colon CFR) Case-Control
2021-12-13
phs002734 Rapid Idiosyncratic Mechanisms of Clinical Resistance to KRAS G12C Inhibition Case Set
2021-12-14
phs002735 Tumor Infiltrating Lymphocytes (TIL) Recognize Unique Somatic Mutations and Mediate Objective Clinical Responses in Metastatic Breast Cancer Cohort
2021-12-15
phs002746 Resistance to Latent Mycobacterium tuberculosis Infection in South Africa: Immunologic Profiling Case-Control
2021-12-16
phs002748 Transcriptome and TCR Sequencing of T Cells from Metastectomies Case Set
2021-12-19
phs002750 Single Cell RNA Sequencing of Human Hematopoiesis Case Set
2021-12-19
phs002752 Clinical Trial of COVID-19 Convalescent Plasma in Outpatients (C3PO) Clinical Trial
2021-12-22
phs002753 Ameloblastoma Cell Line Resource Exome Sequencing
2021-12-22
phs002754 PROGRESS/ELEMENT DNA Methylation Study Cohort
2021-12-26
phs002756 Characterizing the Role of the Immune Microenvironment in Multiple Myeloma Progression at a Single Cell Level Case Set
2021-12-27
phs002758 Single-Cell Analysis of Somatic Mutations in Human Bronchial Epithelial Cells in Relation to Aging and Smoking Cross-Sectional
2022-01-03
phs002762 Functional Multiomics of Cellular Therapy and Immune Checkpoint Blockade Therapy for Solid Tumors Longitudinal
2022-01-10
phs002764 Dissecting Cell Composition and Drug Sensitivity in Human Adenoid Cystic Carcinomas (ACCs) Exome Sequencing
2022-01-11
phs002765 Transcriptomic Profiles of Neoantigen-Reactive T Cells in Human Gastrointestinal Cancers Case Set
2022-01-12
phs002766 Generation of a Cellular Atlas of Human Adipose Tissue Collection
2022-01-12
phs002767 Epidemiologic Architecture for Genes Linked to Environment (EAGLE) MetaboChip Study Electronic Medical Records
2022-01-14
phs002769 Multi-Omic Investigation of Beckwith-Wiedemann Syndrome Wilms Tumor Cohort
2022-01-17
phs002771 SLAMF7 Regulates Synovial Macrophages in Rheumatoid Arthritis Full Transcriptome Sequencing
2022-01-17
phs002774 Center for Common Disease Genomics [CCDG] - Cardiovascular: ENGAGE Atrial Fibrillation-TIMI 48 Case Set
2022-01-18
phs002780 IFN-γ and TNF-α drive a CXCL10+ CCL2+ Macrophage Phenotype Expanded in Severe COVID-19 Lungs and Inflammatory Diseases with Tissue Inflammation RNA Sequencing
2022-01-24
phs002783 Pan Cancer Investigation of Human Leukocyte Antigen Loss of Heterozygosity Case Set
2022-01-24
phs002787 Personalized Breast Cancer Vaccines Based on Genome Sequencing Exome Sequencing
2022-01-26
phs002790 Childhood Cancer Data Initiative (CCDI): Molecular Characterization Initiative Aggregate Genomic Data
2023-02-23
phs002792 Characterization of Neoantigen-reactive T cells by Single-Cell Analysis Case Set
2022-01-31
phs002793 Study of Lyme Immunology and Clinical Events (SLICE) Case-Cohort
2022-09-13
phs002802 Phase IB/II Study of Bazedoxifene in Combination with Palbociclib in Patients with Endocrine Resistant Hormone Receptor-Positive Breast Cancer Prospective
2022-02-09
phs002803 A Phase II Clinical Trial of the PARP Inhibitor Talazoparib in BRCA1 and BRCA2 Wild-Type Patients Clinical Trial
2022-02-09
phs002804 DNA Double Strand Breaks in KMT2A-Rearranged AML patients Case-Control
2022-02-09
phs002808 Nulliparous Pregnancy Outcomes Study: Monitoring Mothers-to-be Heart Health Study (nuMoM2b Heart Health Study) Longitudinal Cohort
2022-02-09
phs002809 Genome-Wide Pleiotropy Scan Across Multiple Cancers Case-Control
2022-02-09
phs002810 Genetic Analysis of Latin American Cervical Cancer Case Set
2022-02-10
phs002811 Center for Common Disease Genomics [CCDG] - Cardiovascular: The Genetics of Atrial Fibrillation Case Set
2022-02-13
phs002812 Multiplexed scRNA-Seq Reveals Cellular and Genetic Correlates of SLE Case-Control
2022-02-13
phs002814 Esophageal Squamous Cell Carcinoma Precursor Study Case Set
2022-02-14
phs002815 Center for Craniofacial and Dental Genetics (CCDG): Genetics of Orofacial Clefts, Sub-types, and Subclinical Phenotypes - CIDR Case-Control
2022-02-15
phs002816 Genetic Diseases of Immune Homeostasis and Autoimmunity Caused by GIMAP Deficiency Exome Sequencing
2022-02-15
phs002817 Mutations in GNAI2 Cause Developmental and Immune Dysregulation Case Set
2022-02-15
phs002818 Intercepting Progression from Pre-Invasive to Invasive Lung Adenocarcinoma Exome Sequencing
2022-02-16
phs002819 Single-Nuclei Paired Multiomic Analysis of Young, Aged, and Parkinson's Disease Human Midbrain Reveals Age-Associated Glial Changes and Their Contribution to Parkinson's Disease Case-Control
2022-02-16
phs002820 Cancer Risk Estimates Related to Susceptibility Genes (CARRIERS) Case-Control
2022-02-16
phs002822 SU2C-MARK Lung Cancer Consortium - Checkpoint Blockade Response Project Clinical Cohort
2022-02-17
phs002826 Analysis of Papilloma Infiltrating T cells from an Exceptional Responder to Immunotherapy Interventional
2022-02-22
phs002833 A Phase 2 Study of Lamivudine in Patients with p53 Mutant Metastatic Colorectal Cancer Clinical Trial
2022-02-27
phs002834 Clinical and Molecular Features of Acquired Resistance to Immunotherapy in Non-Small Cell Lung Cancer Case Set
2022-03-02
phs002835 Breast Cancer Family Registry Cohort
2022-03-02
phs002840 The Transcriptomic Landscape of Oncogenic PI3K Reveals Key Functions in Splicing and Gene Expression Regulation Clinical Trial
2022-03-08
phs002842 Gene Expression in an African American Schizophrenia Dataset RNA Sequencing
2022-03-09
phs002845 Expression of Activation Induced Cytidine Deaminase and Risk of Transformation in Follicular Lymphoma Clinical Cohort
2022-03-12
phs002846 Pharmacogenomics of Mercaptopurine Intolerance in Children with Acute Lymphoblastic Leukemia (AALL03N1) Clinical Cohort
2022-03-14
phs002847 Circulating Tumor DNA as a Biomarker in Patients with Stage III and IV Wilms Tumor: Analysis from a Children's Oncology Group Trial, AREN0533 Case Set
2022-03-14
phs002849 A Sequential Window of Opportunity Trial of Anti-PD-L1/TGF-β trap (M7824) Alone and in Combination with TriAd Vaccine and N-803 for Resectable Head and Neck Squamous Cell Carcinoma not Associated with Human Papillomavirus Infection Prospective
2022-03-20
phs002852 A Pilot Study of NKTR-214 and Nivolumab in Selected Patients with Locally Advanced/Metastatic Sarcoma Clinical Trial
2022-03-22
phs002856 Genomic Studies of Bipolar Disorder in a Large Cohort from The Netherlands Cohort
2022-03-27
phs002857 MSK SPECTRUM - SPatiotemporal Evolution of Cancer Traced Using Multimodalities Case Set
2022-03-28
phs002858 The Mood and Methylation Study (MMS) Epigenetics
2022-03-29
phs002859 RB1 Loss Triggers Dependence on ESRRG in Retinoblastoma Exome Sequencing
2022-03-29
phs002861 Genomic Data Archive From the Network for Pancreatic Organ Donors With Diabetes Case-Control
2022-03-30
phs002862 Improved T Cell Immunity Following Neoadjuvant Chemotherapy in Ovarian Cancer Longitudinal
2022-03-31
phs002863 Genome-Wide Association Study of Heparin-Induced Thrombocytopenia GWAS
2022-04-03
phs002864 Genomic Analyses in Neoadjuvant Immunotherapy-Treated Head and Neck Cancers Clinical Cohort
2022-04-03
phs002865 Accurate Genome-Wide Germline DNA Profiling from Decade-Old Archival Tissue Specimens Sequencing
2022-04-03
phs002866 Circulating Tumor DNA in Intermediate Risk Rhabdomyosarcoma Case Set
2022-04-04
phs002867 Blood Somatic Mutations in TCGA Donors Suffering from Solid Tumors Case Set
2022-04-04
phs002876 CTN - 0051: Extended-Release Naltrexone vs. Buprenorphine for Opioid Treatment (X:BOT) Multicenter
2022-04-06
phs002877 Mapping the Evolution of T Cell States During Response and Resistance to Adoptive Cellular Therapy Longitudinal
2022-04-07
phs002879 Vulnerabilities of Midbrain Dopaminergic Neurons to Parkinson's Disease Revealed by Single-Cell Genomics Cross-Sectional
2022-04-11
phs002881 The Pathogenesis and Genetics of Disseminated Coccidioidomycosis Cohort
2022-04-13
phs002902 Ribosomal Depleted Total RNA-Seq of PBMCs and Skin from Controls and Systemic Sclerosis Patients Case-Control
2022-05-03
phs002903 The Role of CDX2 in Controlling ABCB1 Expression and Chemosensitivity in Human Colon Cancer Marker Discovery
2022-05-03
phs002908 Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Hispanic Community Health Study/Study of Latinos (HCHS/SOL) None
2022-05-05
phs002909 Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Subpopulations and Intermediate Outcome Measures in COPD Study (SPIROMICS) Longitudinal Cohort
2022-05-05
phs002910 Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Genetic Epidemiology of COPD Study (COPDGene) Longitudinal Cohort
2022-05-05
phs002911 Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Framingham Heart Study (FHS) Longitudinal Cohort
2022-05-05
phs002913 Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Severe Asthma Research Program (SARP) Longitudinal Cohort
2022-05-08
phs002914 Ultrasensitive Profiling of UV Mutations in Facial Tumors in TSC Case-Control
2022-05-08
phs002915 Integrative Single-Cell Analysis of Transcriptome, Epigenome, and Lineage in HIV Latency and Activation Case-Control
2022-05-08
phs002919 Collaborative Cohort of Cohorts for COVID-19 Research (C4R): REasons for Geographic and Racial Differences in Stroke (REGARDS) Longitudinal Cohort
2022-05-10
phs002921 Whole Genome Sequencing in the Inner City Asthma Consortium (ICAC) Cohorts Longitudinal
2023-01-09
phs002922 Genomic and Transcriptomic Sequencing of CAR-T-Treated Patients Cohort
2022-05-12
phs002925 Genomic Analysis of Extra-Nodal Natural Killer/T-Cell Lymphoma (ENKTCL) Exome Sequencing
2022-05-17
phs002926 Infant Immune Responses to Early Life Vaccinations Clinical Cohort
2022-05-17
phs002927 Blood Gene Signatures Associated with Stiffness After TKA Case-Control
2022-05-18
phs002928 Adoptive Cell Therapy of Autologous T cell Receptor-Engineered T Cells Targeting the p53 Neoantigens in Human Solid Tumors Clinical Trial
2022-05-18
phs002929 The Genetic Basis of Progression in Multiple Sclerosis GWAS
2022-05-18
phs002931 Decade-Long Leukemia Remissions with Persistence of CD4+ CAR T-Cells Case Set
2022-05-22
phs002933 Single-Cell RNA-Sequencing Analysis of Responses to Pembrolizumab in Sezary Syndrome Single Cell Analysis
2022-05-23
phs002934 Molecular Biomarkers of Obesity and Metformin Response in Endometrial Cancer: Analysis of GOG-0286B Case Set
2022-05-24
phs002935 Transcriptomic Profiling of Oropharyngeal Squamous Cell Carcinoma Case Set
2022-05-24
phs002937 Exploring the Genomic Dark Matter of Neurodevelopmental Disorders Case-Control
2022-05-31
phs002939 NCI-Maryland Prostate Cancer Case-Control Study Case-Control
2022-06-03
phs002940 PRE-DETERMINE: Biologic Markers and MRI SCD Cohort Study Longitudinal Cohort
2022-06-05
phs002941 CALGB/SWOG 80405 ct DNA Biomarker Evaluation Longitudinal
2022-06-05
phs002944 Melanoma Brain Metastasis Single-Cell RNA Sequencing Atlas Cohort
2022-06-06
phs002950 Methylation Profiles of Cell-Free DNA Using Nanopore Sequencing Case-Control
2022-06-08
phs002959 Joslin Study on the Genetics of Type 2 Diabetes Family
2022-06-13
phs002960 Exploring the Microbiome-Gut-Brain Axis with Respect to Psychoneurological Symptoms for Children with Solid Tumors Case-Control
2022-06-13
phs002962 Germline Genetics of Myelodysplastic Syndromes (MDS) and Acute Myeloid Leukemia (AML) Case-Control
2022-06-14
phs002966 Single-Cell Analysis of CD19-Specific CAR T Cell Treatment of Relapsed/Refractory CD19+ Acute Lymphoblastic Leukemia Clinical Cohort
2022-06-16
phs002968 Inherited T Cell Defects: Diagnosis, Mechanisms and Treatments Exome Sequencing
2022-06-17
phs002973 Genomic Translation for ALS Care (GTAC) - WGS Case Set
2022-06-26
phs002977 Functional Analysis of Genetic Variants in African Americans with Breast Cancer Affected Sib Pairs
2022-06-28
phs002978 AC-ICAM: An Atlas and Compass of Immune-CAncer-Microbiome Interactions in Colon Cancer Case-Cohort
2022-06-28
phs002979 Evaluation of Nuclear DNA from Rootless Hairs for Forensic Purposes Genotype
2023-06-27
phs002980 Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Mediators of Atherosclerosis in South Asians Living in America Study (MASALA) Cohort
2022-06-29
phs002981 INCLUDE: Human Trisome Project None
2022-06-29
phs002982 INCLUDE: The Epidemiology of Transient Leukemia in Newborns with Down Syndrome None
2022-06-29
phs002983 INCLUDE: Genetic Underpinnings of the Multifactorial Phenotype of Trisomy 21 Patients Unveiled by Multi-Omics Approaches None
2022-06-29
phs002985 Center for Common Disease Genomics [CCDG] - Cardiovascular: Pharmacokinetic Polymorphisms in Japanese General Population Control Set
2022-07-04
phs002986 A Randomized Multi-Institutional Phase II Trial of Everolimus as Adjuvant Therapy in Patients with Locally Advanced Squamous Cell Cancer of the Head and Neck Case Set
2022-07-04
phs002988 Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Atherosclerosis Risk in Communities Study (ARIC) Longitudinal Cohort
2022-07-05
phs002989 Genomic Analysis of Follicular Lymphoma Case Set
2022-07-05
phs002990 Investigation of the Causal Etiology in a Patient with T-B+NK+ Immunodeficiency Exome Sequencing
2022-07-06
phs002991 Improving Transcriptome Fidelity Following Synovial Tissue Disaggregation Case Set
2022-07-11
phs002994 BRCA Mutation Status Shapes the Microenvironment of Pancreatic Adenocarcinoma Cohort
2022-07-14
phs002996 Biological Determinants of Peritoneal Dialysis Outcomes GWAS
2022-07-18
phs002997 Genetic Analysis of Syndromic Orofacial Clefting Case-Control
2022-07-19
phs002998 Immune Profiles Study Case Set
2022-07-20
phs002999 Uncovering Inversion Formation in the Human Genome and its Impact to Disease Case Set
2022-07-21
phs003000 ALLELE Consortium Glioblastoma Project Case-Control
2022-07-24
phs003001 Assessment of RNA-Seq Sample Preparation Methodology Case-Control
2022-07-25
phs003002 A Platform Study of Combination Immunotherapy for the Neoadjuvant and Adjuvant Treatment of Patients with Surgically Resectable Adenocarcinoma of the Pancreas Clinical Trial
2022-07-25
phs003003 Gene Expression between PMD and Control LCLs at Baseline, E2, and E2 Withdrawal Case-Control
2022-07-25
phs003005 Somatic Mutations in Single Human Neurons from Patients with Congenital Neurodegenerative Diseases Case-Control
2022-07-30
phs003006 Transcriptional and Epigenetic Profiles of Male Breast Cancer at Single-Cell Resolution Nominate Salient Cancer Specific Enhancers Case Set
2022-07-31
phs003008 Comprehensive Genomic Characterization of Translocation Renal Cell Carcinoma Case Set
2022-07-31
phs003009 Genomic Characterization of Duke Melanoma Brain Metastases Case Set
2022-08-01
phs003010 Center for Common Disease Genomics [CCDG] - Cardiovascular: TexGen Case Set
2022-08-01
phs003011 APOLLO1: Proteogenomic Analysis of Lung Adenocarcinoma Tumor
2022-08-01
phs003014 NCI's Datasets for General Research Use None
2022-08-03
phs003015 Ipilimumab and Decitabine in Treating Patients With Relapsed or Refractory Myelodysplastic Syndrome or Acute Myeloid Leukemia Case Set
2022-08-03
phs003016 Coagulation and Fibrinolysis in a Pediatric Insulin Titration Trial Clinical Trial
2022-08-03
phs003017 Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Multi-Ethnic Study of Atherosclerosis (MESA) Longitudinal Cohort
2022-08-03
phs003019 Phase I Study of the Oral PI3kinase Inhibitor BKM120 or BYL719 and the Oral PARP Inhibitor Olaparib in Patients with Recurrent Triple Negative Breast Cancer or High Grade Serous Ovarian Cancer Clinical Trial
2022-08-06
phs003020 Molecular Analysis of Short- Versus Long-Term Survivors of High-Grade Serous Ovarian Carcinoma Copy Number Variation (CNV)
2022-08-08
phs003022 Circulating Tumor DNA Sequencing Provides Comprehensive Mutation Profiling for Pediatric Central Nervous System Tumors Cohort
2022-08-11
phs003023 Whole-Genome Sequencing Reveals Complex Genomic Features Underlying Anti-CD19 CAR T-Cell Treatment Failure in Lymphoma Whole Genome Sequencing
2022-08-11
phs003024 Gene Expression Analysis in Clonal Evolution of Fanconi Anemia Case Set
2022-08-11
phs003025 Genetic Analysis of Substance Use Disorder Using the Indiana Biobank Data Case-Control
2022-08-14
phs003028 Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Northern Manhattan Study (NOMAS) None
2022-08-14
phs003035 Genomic Analysis of Nucleic Acid Sequences from Pancreatic Cancer Sequencing
2022-08-17
phs003036 Single Cell Genome Variation Induced by Mutational Processes in Cancer - HGSOC Trios Study Tumor vs. Matched-Normal
2022-08-17
phs003038 Exploiting New Patterns of Genome Damage in Triple Negative Breast Cancer Tumor vs. Matched-Normal
2022-08-18
phs003041 Mayo Clinic Adult Diffuse Glioma Illumina OncoArray SNP data Case Set
2022-08-21
phs003042 Novel Strategies to Eliminate Resistance to B-cell Receptor Inhibitor Therapy in Lymphoid Malignancies Case Set
2022-08-23
phs003043 A Pilot Study to Evaluate Tissue- and Plasma-based DNA Driver Mutations in a Cohort of Patients with Pancreatic Intraductal Papillary Mucinous Neoplasms Sequencing
2022-08-23
phs003044 NCI's Collection of Datasets for Health, Medical, and Biomedical Research Purposes None
2022-08-23
phs003046 Epigenetic Biomarkers of Aging Epigenetics
2022-08-29
phs003047 NHGRI GREGoR Consortium: Genomics Research to Elucidate the Genetics of Rare Disease Case Set
2022-08-30
phs003048 Juvenile Sjogren's Syndrome (JSS) Transcriptome Study Case-Control
2022-08-31
phs003053 Resilience and Susceptibility Patterns in the Viral Immune Response Using RNA-Seq (ReSP VIRUS Study) Cross-Sectional
2022-09-05
phs003054 Extracellular RNA Profiling of Serum, Plasma, and Urine of Healthy Subjects Longitudinal
2022-09-08
phs003059 Metastatic Colorectal Adenocarcinoma Tumor Purity Assessment from Whole Exome Sequencing Data Case Set
2022-09-12
phs003060 Whole Exome Sequencing of Calcitonin Producing Pancreatic Neuroendocrine Neoplasms (CT-pNENs) Indicates a Unique Molecular Signature Clinical Cohort
2022-09-13
phs003062 De Novo Characterization of Cell-Free DNA Fragmentation Hotspots in Plasma Whole-Genome Sequencing Case-Control
2022-09-15
phs003063 COVID-19: Post-Hospital Thromboprophylaxis A Multicenter, Adaptive, Prospective, Randomized Trial Evaluating the Efficacy and Safety of Antithrombotic Strategies in Patients with COVID-19 Following Hospital Discharge (ACTIV-4C) Clinical Trial
2022-09-15
phs003064 Phenotypic Signatures of Circulating Neoantigen-Reactive CD8+ T Cells in Patients with Metastatic Cancers Case Set
2022-09-18
phs003065 Uncovering RNA Signatures of C9orf72-Linked ALS and Related Disorders Case-Control
2022-09-19
phs003066 Urothelial Cancer - Genomic Analysis to Improve Patient Outcomes and Research (UC-GENOME): A Bladder Cancer Advocacy Network (BCAN)-Led Collaborative Research Pilot Study Prospective
2022-09-21
phs003067 Using NGS to Sequence Whole Genomes to Identify Genes Underlying ALS Case-Control
2022-09-21
phs003068 Nanobody-Tethered Transposition Allows for Multifactorial Chromatin Profiling at Single-Cell Resolution Epigenetics
2022-09-25
phs003070 Single Cell RNA-Sequencing in Adenoid Cystic Carcinoma Case Set
2022-09-29
phs003071 POISED (Peanut Oral Immunotherapy: Safety, Efficacy, and Discovery) Clinical Trial
2022-09-30
phs003072 RNA-Seq of Whole Blood from Patients with Intracranial Aneurysms Collection
2022-10-02
phs003074 A National Translational Science Network of Precision-Based Immunotherapy for Primary Liver Cancer (PLC) Longitudinal
2022-10-03
phs003075 Longitudinal Studies of Patients with Familial Platelet Disorder with Associated Myeloid Malignancy (FPDMM) Exome Sequencing
2022-10-03
phs003077 Retinoblastoma Aqueous Humor Liquid Biopsy Repository Clinical Cohort
2022-10-05
phs003079 Spatiotemporal Evolution of the ccRCC Microenvironment Links Intra-Tumoral Heterogeneity to Immune Escape CINOMA Clinical Trial
2022-10-06
phs003080 Cell and Circuit-Specific Exploration of HIV Neurogenomics in Context of Opiate and Cocaine Misuse Epigenetics
2022-10-09
phs003084 Genome Sequencing of Circulating Tumor Cells for Minimally Invasive Molecular Characterization of Multiple Myeloma Pathology Tumor vs. Matched-Normal
2022-10-11
phs003085 RNA-Sequencing of B-Lymphoblastic Leukemia with Glucocorticoids and PI3K Delta Inhibition Case Set
2022-10-11
phs003086 Single Cell Transcriptomic Data from CD4+ T Cells from Children with MIS-C Case-Control
2022-10-12
phs003090 Advancing Precision Oncology in a Humanized, Fully Autologous Mouse Model Cohort
2022-10-13
phs003091 Single-Cell DNA Methylation Profiling with sciMETv2 Epigenetics
2022-10-17
phs003093 The Genomic Landscape of Interval Colorectal Cancers Exome Sequencing
2022-10-18
phs003094 Urothelial Cancer - Genomic Analysis to Improve Patient Outcomes and Research (UC-GENOME): a Bladder Cancer Advocacy Network (BCAN)-Led Collaborative Research Pilot Study - for Samples Collected at Johns Hopkins Prospective
2022-10-18
phs003095 Transcriptomic Analysis of HIV-Infected Cells Clinical Cohort
2022-10-18
phs003096 African Demographic History Study Based on WGS Data Cohort
2022-10-18
phs003097 Multi-Modal Single-Cell and Whole-Genome Sequencing of Small, Frozen Clinical Specimens Cohort
2022-10-19
phs003099 Integration of Clinical and Molecular Biomarkers for Melanoma Survival (Berwick) Case-Control
2022-10-20
phs003100 Whole-Genome Sequencing Analysis of Extrachromosomal DNA with Amplicon Architect Tumor
2022-10-23
phs003101 A Model of Human Asthma Exacerbation Identifies Mechanisms That Drive Allergic Asthma Case-Control
2022-10-23
phs003102 Multivalent State Transitions Shape the Intratumoral Composition of Small Cell Lung Carcinoma RNA Sequencing
2022-10-23
phs003103 Single Cell Analysis of Sporadic Human Basal Cell Carcinomas Case Set
2022-10-24
phs003105 Genetic and Phenotypic Analysis of Multiple Sclerosis in Hispanics Case-Control
2022-10-31
phs003106 Genetic Effects on miRNA Expression During Mid-Gestation Neocortical Development eQTL
2022-11-01
phs003108 Role of Genetic Factors in the Pathogenesis of Lung Disease Case Set
2022-11-02
phs003109 Oral Immunotherapy for Induction of Tolerance and Desensitization in Peanut-Allergic Children (IMPACT) Clinical Trial
2022-11-03
phs003110 Clonally selected lines after CRISPR/Cas editing are not isogenic Case Set
2022-11-06
phs003111 Childhood Cancer Data Initiative (CCDI): Clonal Evolution During Metastatic Spread in High-Risk Neuroblastoma Longitudinal Cohort
2022-11-08
phs003112 Transcriptomics of Liver and PBMCs in Alcohol-Associated Liver Disease Case-Control
2022-11-08
phs003113 Integrative Analysis for Multi-Omics Data in Non-Small-Cell Lung Cancer Epigenetics
2022-11-09
phs003115 Genetics of Male Infertility Initiative (GEMINI) Exome Sequencing
2022-11-13
phs003117 Multiregional Single-Cell Transcriptomic Analysis of Liver Cancer Case Set
2022-11-14
phs003118 Cognitively Affected DMD Patients have Unique Methylation Signatures Compared to Cognitively Normal DMD Patients Epigenetics
2022-11-15
phs003121 Targeted Genomic Sequencing in Large Human Genes to Detect Induced Structural Variants Copy Number Variation (CNV)
2022-11-19
phs003122 Human Blastocyst 10X Single Cell RNA Sequencing RNA Sequencing
2022-11-20
phs003131 NHLBI's Collection of Datasets for General Research Use (Public Posting of Genomic Summary Results: Not Allowed) Collection
2022-11-22
phs003132 NHLBI's Collection of Datasets for General Research Use (Public Posting of Genomic Summary Results: Allowed) None
2022-11-22
phs003133 NHLBI's Collection of Datasets for Health / Medical / Biomedical Research Use (Public Posting of Genomic Summary Results: Not Allowed) Collection
2022-11-22
phs003134 NHLBI's Collection of Datasets for Health / Medical / Biomedical Research Use (Public Posting of Genomic Summary Results: Allowed) None
2022-11-22
phs003136 African American Adolescent Idiopathic Scoliosis Whole Genome and Whole Exome Study Case Set
2022-11-22
phs003138 3/7 Psychiatric Genomics Consortium: Finding Actionable Variation Case-Control
2022-11-27
phs003139 Genetic Progression of Head and Neck Squamous Cell Carcinoma Cohort
2022-11-27
phs003140 Genetic Epidemiology of Ovarian Cancer Histotypes Case Set
2022-11-28
phs003141 Integrative Somatic and Germline Computational Biology to Redefine Clinical Actionability in Solid Tumors Case Set
2022-12-05
phs003143 My Pediatric and Adult Rare Tumor (MyPART) Natural History Study of Rare Solid Tumors Clinical Cohort
2022-12-05
phs003145 Tissue Sampling and Biorepository to improve Cancer Cell Therapy Case Set
2022-12-06
phs003146 Predicting the Prevalence of Complex Genetic Diseases from Individual Genotype Profiles Using Capsule Networks Genotype
2022-12-06
phs003147 A Phase II Neoadjuvant Study of Palbociclib in Combination with Letrozole and Trastuzumab as Neoadjuvant Treatment of Stage II-III ER+ HER2+ Breast Cancer (PALTAN) Clinical Trial
2022-12-06
phs003148 NCT03343197: Clinical Biomarker Data Clinical Trial
2022-12-06
phs003149 Bladder Cancer Organoids as a Functional System to Model Different Disease Stages and Therapy Response Case Set
2022-12-06
phs003150 International Cancer Proteogenomics Consortium (ICPC): Proteogenomics of East-Asian Breast Cancer Exome Sequencing
2022-12-06
phs003151 Genetics of Glucose Regulation in Gestation and Growth (Gen3G) Cohort - Placenta Transcriptomics RNA Sequencing Cohort
2022-12-07
phs003152 CPTAC: Proteogenomic Studies of Ovarian Tumor Responses to Agents Targeting the DNA Damage Response Case Set
2022-12-07
phs003153 Neoantigen-Targeted CD8+ T-Cell Responses 1 With PD-1 Blockade Therapy Case Set
2022-12-11
phs003154 An Advanced Molecular Medicine Case Report of a Rare Human Tumor Using Genomics, Pathomics, and Radiomics Case-Control
2022-12-13
phs003155 TCGA WGS Variants Across 18 Cancer Types GWAS
2022-12-14
phs003156 Developing Biomarkers Incorporating High Throughput RNA, DNA, Small RNA Sequencing and Protein Expression in Inflammatory Bowel Disease Using Formalin-Fixed, Paraffin-Embedded (FFPE) Tissue Samples Case-Control
2022-12-14
phs003158 Sézary Syndrome Originates from Heavily Mutated Hematopoietic Progenitors Case Set
2022-12-18
phs003159 Targeted Long-Read Sequencing of the Ewing Sarcoma 6p25.1 Susceptibility Locus Case-Control
2022-12-19
phs003164 Childhood Cancer Data Initiative (CCDI): CCDI Pediatric In Vivo Testing Program - Leukemia Copy Number Variation (CNV)
2022-12-21
phs003165 Phase I Study and Cell-Free DNA Analysis of T-DM1 and Metronomic Temozolomide for Secondary Prevention of HER2-Positive Breast Cancer Brain Metastases Case Set
2022-12-21
phs003166 Enhancing Open Data Sharing for Functional Genomics Experiments: Measures to Quantify Genomic Information Leakage and File Formats for Privacy Preservation Genotype
2022-12-24
phs003168 Phenotypic and Genotypic Study of Keratoconus Case Set
2022-12-26
phs003169 Extracellular microRNA Biomarkers for Diagnostic and Prognostic Assessment of Preeclampsia at Triage Case-Control
2022-12-26
phs003170 Genome-Wide Analysis of Aberrant Position and Sequence of Plasma DNA Fragment Ends in Patients With Cancer Case-Control
2022-12-30
phs003172 Malnutrition and Enteric Disease Network (Mal-ED) Birth Cohort in Brazil Prospective
2023-01-09
phs003173 Malnutrition and Enteric Disease Network (Mal-ED) Case-Control Study in Brazil Prospective
2023-01-09
phs003174 Intervention with Micronutrients and Long-Term Impact in Brazil-RECODISA Prospective
2023-01-09
phs003175 Long-term Impact and Intervention with Micronutrients in Brazil, Parque Universitário, Community-Based Study Randomized
2023-01-09
phs003177 Comparison Between qPCR and RNA-Seq Reveals Challenges of Quantifying HLA Expression Genotype/Expression
2023-01-10
phs003178 Combined PDCD1, BRAF and MAP2K7 Inhibition in BRAFV600E Colorectal Cancer: A Phase 2 Trial Case Set
2023-01-10
phs003179 Rheumatoid Arthritis Finger Stick RNA Sequence Data Observational
2023-01-11
phs003180 Eosinophil Activation and Function in Parasitic Infections and Other Conditions with Increased Tissue or Peripheral Blood Eosinophilia in Humans Whole Genome Sequencing
2023-01-15
phs003182 Reference Profiles of ExRNAs in Normal Human Pregnancy Case-Control
2023-01-19
phs003183 The Ultrasound Study of Tamoxifen Cohort
2023-01-19
phs003184 ALS Compute Case-Control
2023-01-19
phs003185 Molecular Subtyping Reveals Immune Alterations Associated with Progression of Bronchial Premalignant Lesions Clinical Cohort
2023-01-23
phs003186 Tamoxifen Response at Single Cell Resolution in Estrogen Receptor Positive Primary Human Breast Tumors Case Set
2023-01-25
phs003187 LCLF1.0 Data RNA Sequencing
2023-01-26
phs003188 Overcoming Clinical Resistance to EZH2 Inhibition Using Rational Epigenetic Combination Therapy Clinical Cohort
2023-01-26
phs003189 Genetics of Antinuclear Antibodies Case-Control
2023-01-30
phs003190 Extrachromosomal DNA Amplification Contributes to Small Cell Lung Cancer Heterogeneity and is Associated with Worse Outcomes Observational
2023-01-30
phs003191 RNA Splicing Dysregulation in the Pathogenesis of Chronic Lymphocytic Leukemia Cohort
2023-01-30
phs003192 ARST17B2-Q Germline and Somatic Genetic Landscape of Pediatric Rhabdomyosarcoma Case Set
2023-02-02
phs003194 Maternal and Developmental Risks from Environmental and Social Stressors (MADRES) Center for Environmental Health Disparities Cohort
2023-02-05
phs003195 NSD2 E1099K Drives Relapse in Pediatric Acute Lymphoblastic Leukemia by Disrupting 3D Chromatin Organization Phase III
2023-02-06
phs003196 Detection and Targeting of Splicing Deregulation in Pediatric Acute Myeloid Leukemia Stem Cells Case-Control
2023-02-06
phs003197 Genetic Study of Vascular Anomalies Case Set
2023-02-07
phs003198 Genomic Analyses of Germline and Somatic Variation in High-Grade Serous Ovarian Cancer Case Set
2023-02-07
phs003199 RNA-Seq Data From Early Stage Triple Negative Breast Cancer Tumors Treated With TVEC and Chemotherapy (MCC18621) Case Set
2023-02-07
phs003200 High-Throughput RNA Isoform Sequencing using Programmable cDNA Concatenation Methods Development
2023-02-09
phs003201 E5103 Correlative Studies Case-Control
2023-02-12
phs003202 Joint Addiction, Aging, and Mental Health (JAAMH) Data Access Committee General Research Use Datasets Collection
2023-02-12
phs003203 A Comprehensive Platform for Analyzing Longitudinal Multi-Omics Data Epigenetics
2023-02-12
phs003207 Single Cell Colony Whole Genome Sequencing Data From Individuals With Telomere Syndromes Case-Control
2023-02-13
phs003208 Transcriptomic Profiling of Bulk Tissue and Laser-Capture Microdissected Neurons of Postmortem Human Brains in the Superior Temporal Gyrus RNA Sequencing
2023-02-13
phs003209 Structurally Complex Osteosarcoma Genomes Exhibit Limited Heterogeneity within Individual Tumors and across Evolutionary Time Copy Number Variation (CNV)
2023-02-14
phs003210 The Nephrotic Syndrome Study Network (NEPTUNE) Longitudinal Cohort
2023-02-15
phs003212 A Pilot Trial of Complement Inhibition Using Eculizumab to Overcome Platelet Transfusion Refractoriness in HLA Allo-Immunized Patients Clinical Trial
2023-02-22
phs003213 Melbourne Collaborative Cohort Study DNA Methylation Studies Longitudinal
2023-02-23
phs003214 NPC Genome Project Case Set
2023-02-23
phs003216 Whole Genome Sequencing Analysis in a Family of Discordant Twins With Non-Syndromic Microtia and Hemifacial Microsomia: Identification of Novel Candidate Genes and Variants Case-Control
2023-02-28
phs003217 Molecular Determinants of Esophageal Cancer in Tanzania Cohort
2023-02-28
phs003218 Whole Exome Sequencing and RNA-Seq to Characterize the Somatic Breast Cancer Landscape Among Latinas in California Case Set
2023-03-01
phs003219 Single-Cell Sequencing Reveals Distinct Microenvironment Cell Types Associated with Response to High Dose Melphalan and Autologous Stem Cell Transplant in Multiple Myeloma Case Set
2023-03-06
phs003220 Identification of High-Risk PHF19 Expressing Cells in Myeloma Single-Cell Multiomics Single Cell Analysis
2024-03-31
phs003221 Sudden Death in the Young Case Registry Case Set
2023-03-06
phs003223 DIGEST: Dietary Influences on Glucuronidation, a Cross-Sectional Study of Diet and Metabolism Control Set
2023-03-08
phs003227 Hi-C Profiling of Solid Tumor Samples Case Set
2023-03-12
phs003228 Genomics of Blastic Plasmacytoid Dendritic Cell Neoplasm Longitudinal
2023-03-12
phs003229 Analysis of Donor Pancreata Defines the Transcriptomic Signature and Microenvironment of Early Neoplastic Pancreatic Lesions Observational
2023-03-16
phs003230 Temporal Evolution Reveals Bifurcated Lineages in Aggressive Neuroendocrine Small Cell Prostate Cancer Trans-Differentiation Longitudinal
2023-03-16
phs003231 ApoA-1 and Atherosclerosis in Psoriasis Longitudinal
2023-03-19
phs003233 Single Cell Genotypic and Phenotypic Analysis of Measurable Residual Disease in Acute Myeloid Leukemia Clinical Genetic Testing
2023-03-21
phs003234 Rapid Acceleration of Diagnostics - Underserved Populations (RADx-UP): COVID-19 Testing and Vaccination Social Network Diffusion for Diverse Criminal Legal Involved Communities Controlled Trial
2023-03-21
phs003240 Binding of Epstein Barr Virus EBNA2 Unifies Multiple Sclerosis Genetic Mechanisms Case-Cohort
2023-03-23
phs003242 TREM2+ Cells in Human Basal Cell Carcinomas Case Set
2023-03-23
phs003243 Comprehensive Omics Analysis of Pediatric Solid Tumors and Establishment of a Repository for Related Biologic Studies (10C0086) Observational
2023-03-24
phs003245 Phenotyping and Therapeutic Approaches for Patients with Sellar/Suprasellar Disorders Case Set
2023-03-28
phs003246 Multimodal Immune Profiling to Determine Mechanisms of COVID-19 Clinical Trajectory in Uganda Clinical Cohort
2023-03-29
phs003249 Deterministic Evolution and Stringent Selection During Pre-Neoplasia Copy Number Variation (CNV)
2023-04-01
phs003250 Therapeutic Genetics and Disease Modeling in LAMA2-CMD Interventional
2023-04-01
phs003255 Single Duplex DNA Sequencing with CODEC Detects Mutations with High Sensitivity Case-Control
2023-04-06
phs003256 Therapy-Induced APOBEC3A Drives Evolution of Resistance to Targeted Therapies in Non-Small Cell Lung Cancer Individual-Level Genomic Data
2023-04-09
phs003257 Investigating the Role of Neddylation in the Repair of Topoisomerase I-Mediated DNA Damage in Colorectal Cancer Cohort
2023-04-10
phs003260 Single Nucleus Transcriptomes from the Ventral Midbrain of Opioid Overdose Cases and Controls Cohort
2023-04-11
phs003261 Studies in the Pathogenesis of Systemic Capillary Leak Syndrome (SCLS, Clarkson Disease) Case-Control
2023-04-12
phs003268 Maintenance of Brain Tumor Profile on Organotypic Brain Slice Culture (OBSC) Case Set
2023-04-13
phs003269 GATA2 Deficiency and the MonoMAC Syndrome Case-Cohort
2023-04-13
phs003270 Studies in the Natural History and Pathogenesis of Childhood-Onset and Adult-Onset Idiopathic Inflammatory Myopathies Case-Control
2023-04-13
phs003271 A Scalable, GMP-Compatible, Autologous Organotypic Cell Therapy for Dystrophic Epidermolysis Bullosa Case Set
2023-04-16
phs003272 Supraphysiologic MDM2 Expression Impacts P53-Independent Chromatin Networks and Therapeutic Responses in Sarcoma Cohort
2023-04-16
phs003275 Prediction of Resistance and Sensitivity to HER2 Targeted Therapy in the Neoadjuvant Setting Case Set
2023-04-18
phs003277 Cellular Indexing of Transcriptomes and Epitopes Sequencing (CITE-Seq) Analysis to Investigate the Impact of Granulocyte-Colony Stimulating Factor on CRISPR/Cas9 Gene Edited Human Hematopoietic Stem Cell Function RNA Sequencing
2023-04-19
phs003278 Sex Chromosome Aneuploidy Effects on Human Gene Expression Case-Control
2023-04-19
phs003279 MAITS in HCC Single Cell Analysis
2023-04-23
phs003282 Genetic Analysis of Skin Cells Aggregate Genomic Data
2023-04-25
phs003283 eIMPACT Trial: Modernized Collaborative Care to Reduce the Excess CVD Risk of Older Depressed Patients Clinical Trial
2023-04-25
phs003284 Immune-Related Adverse Events after Immune Checkpoint Blockade-Based Therapy are Associated with Improved Survival in Advanced Sarcoma Clinical Trial
2023-04-26
phs003286 Multi-Omic Profiling of Glioma Patient Tumors and Patient-Derived Model Systems Exome Sequencing
2023-04-30
phs003287 FinaleMe: Predicting DNA Methylation by the Fragmentation Patterns of Plasma Cell-Free DNA Epigenetics
2023-04-30
phs003288 Multi-Ethnic Study of Atherosclerosis (BioLINCC) Family
2023-05-01
phs003290 Cell-Free, Methylated DNA in Blood Samples Reveals Tissue-Specific, Cellular Damage from Radiation Treatment Epigenetics
2023-05-04
phs003297 Population Genetic Testing and SERPINA1 Sequencing Identifies Unidentified Alpha-1 Antitrypsin Deficiency Alleles and Gene-Environment Interaction with Hepatitis C Infection Clinical Diagnostic Testing
2023-05-08
phs003298 Genetics and Functional Studies of Autosomal Recessive Neurological Disorders Family
2023-05-10
phs003300 Small RNA Contents of Extracellular Vesicles from Patients with Cognitive Decline Case-Control
2023-05-11
phs003302 Epigenetic Landscape of Human Parathyroids Collection
2023-05-16
phs003303 Molecular and Clinical Analyses of PHF6 Mutant Myeloid Neoplasia Provide Clues as to Their Pathogenesis and Therapeutic Targeting Cohort
2023-05-17
phs003304 Adipocytes Regulate Fibroblast Function and Their Loss Contributes to Fibroblast Dysfunction in Inflammatory Diseases RNA Sequencing
2023-05-17
phs003306 Characterization of Macrophage-Tropic HIV Infection of Central Nervous System Cells and the Influence of Inflammation Case Set
2023-05-18
phs003307 Global Endometrial DNA Methylation Analysis Reveals Insights into mQTL Regulation and Associated Endometriosis Disease Risk and Endometrial Function Case-Control
2023-05-21
phs003308 Whole Exome Sequencing Analysis of Carfilzomib-Related Cardiotoxicity in Multiple Myeloma Patients Clinical Cohort
2023-05-22
phs003310 Type I Interferon and Cycling Lymphocytes in Macrophage Activation Syndrome Case-Control
2023-05-24
phs003312 PD-1 Instructs a Tumor Suppressive Metabolic Program to Restrain AP-1 Activity in T Cell Lymphoma Case Set
2023-05-25
phs003313 RNA-Seq from PMM2-CDG Patients and Healthy Controls Case-Control
2023-05-30
phs003315 A Microwell Platform for High-Throughput Longitudinal Phenotyping and Selective Retrieval of Organoids Copy Number Variation (CNV)
2023-05-30
phs003316 A Pilot Study of Neoadjuvant Nivolumab, Ipilimumab and Intralesional Oncolytic Virotherapy for HER2-Negative Breast Cancer Cohort
2023-06-04
phs003317 Integrative Age-Related Changes in Genome and Epigenome in Human Lung in Relation to Smoking Case-Control
2023-06-06
phs003318 Single-Cell Multi-Omic Analysis of the Vestibular Schwannoma Ecosystem Uncovers a Nerve Injury-Like State Case Set
2023-06-07
phs003319 Interruption of BTK Inhibitor Improves Response to SARS-CoV-2 Booster Vaccination in Patients with Chronic Lymphocytic Leukemia Clinical Cohort
2023-06-08
phs003320 RNA Sequencing of ECOG-E1308 Case Set
2023-06-12
phs003321 DNA Methylation Studies in CREW Cohorts (URECA and COAST) Case-Control
2023-06-14
phs003322 Integrated Analysis of Multimodal Single-Cell Datasets for SARS-CoV-2 Vaccination Sequencing
2023-06-18
phs003326 Microvascular Permeability, Inflammation, and Lesion Physiology in Endometriosis: A Microphysiological Systems Approach Case-Control
2023-06-22
phs003327 Experimental and Clinical Studies of Presbycusis Cohort
2023-06-25
phs003328 Genetic Causes of Congenital Anosmia Case-Control
2023-06-26
phs003330 Uveal Melanoma Immunogenomics Predict Immunotherapy Resistance and Susceptibility RNA Sequencing
2023-06-28
phs003338 BarcUVa-Seq (Biology of Colorectal Cancer Risk Enhancers) Cohort
2023-07-02
phs003342 Meta-Analysis of Genome-Wide Association Studies of Bladder Cancer Risk Case-Control
2023-07-10
phs003343 Targeted Linked-Read DNA-seq Analysis of Castration-Resistant Prostate Cancers Case Set
2023-07-10
phs003346 Method to Assess Lung Water Accumulation During Exercise Methods Development
2023-07-12
phs003348 A genotype-phenotype study of tumors from patients with inherited mutations in DNA repair genes Clinical Cohort
2023-07-16
phs003349 Single-Cell Transcriptomics of Adult Recurrent Respiratory Papillomatosis Case Set
2023-07-17
phs003350 Diabetes Multi-Omic Investigation of Drug Response (DIAMOND) Longitudinal Cohort
2023-07-17
phs003351 Single Cell Analysis of Psoriasis Resolution following IL-23 Blockade Cohort
2023-07-18
phs003356 ChiLDReN/BA: Genetic Studies of Biliary Atresia in the Childhood Liver Disease Research Network Cohort
2023-07-20
phs003358 Patient Microbiome and Surgical Site Infection in Spine Surgery Case Set
2023-07-24
phs003361 Rapid Acceleration of Diagnostics - Underserved Populations (RADx-UP): COVID-19 Testing and Prevention in Correctional Settings Collection
2023-07-25
phs003369 The Melbourne Urological Research Alliance (MURAL) Collection of Patient-Derived Models of Prostate Cancer RNA Sequencing
2023-07-30
phs003370 Genetic Predictors of Ibrutinib-Related Cardiovascular Side Effects in Patients with Chronic Lymphocytic Leukemia Case-Control
2023-07-31
phs003378 A Phase I Study of the Treatment of Recurrent Malignant Glioma with CAN-3110 (AKA rQNestin34.5v.2), a Genetically Engineered HSV-1 Virus Clinical Cohort
2023-08-02
phs003379 Germline Mutations and Developmental Mosaicism Underlying EGFR-Mutant Lung Cancer Case Set
2023-08-02
phs003381 Cryptic Splice Mutation in the Fumarate Hydratase Gene in Patients With Clinical Manifestations of Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) Case Set
2023-08-07
phs003389 Genomic Studies in Charcot-Marie-Tooth Disease Case Set
2023-08-15
phs003390 Adipose Tissue Omics In Obesity Case Set
2023-08-16
phs003392 Epigenetic Changes in Immune Response and Oncogenesis Related Genes Caused by Heavy Metal Long-Term Exposure Case-Control
2023-08-17
phs003395 Efficacy of Ustekinumab Followed by Abatacept for the Treatment of Psoriasis Vulgaris (PAUSE) Clinical Trial
2023-08-17
phs003398 Non-Coding Mutations Cause Enhancer Targeting Resulting in Protein Synthesis Dysregulation During B-Cell Lymphoma Progression Tumor vs. Matched-Normal
2023-08-17
phs003399 Reference Standards for Mosaic Variant Detection Exome Sequencing
2023-08-18
phs003400 Dysregulation of Naive T Cell Quiescence during Aging Cross-Sectional
2023-08-20
phs003402 Genomic Tumor Correlates of Clinical Outcomes Following Organ-Sparing Chemoradiation Therapy for Bladder Cancer Case Set
2023-08-26
phs003403 Circulating RNAs in Acute Heart Failure (CRUCIAL) Cohort
2023-08-27
phs003404 Genomic Analysis of Prostate Tumor Heterogeneity in Metastasis Tumor vs. Matched-Normal
2023-08-28
phs003408 MILK-Omics: Systems Biology of Human Milk and Its Links to Maternal and Infant Health Cohort
2023-08-29
phs003410 A Human Lymphoma Organoid Model for Evaluating and Targeting the Follicular Lymphoma Tumor Immune Microenvironment Case Set
2023-08-31
phs003412 A Phase III Randomized Study of Nivolumab Plus Ipilimumab Versus Nivolumab in Stage IV Squamous Cell Lung Cancer Controlled Trial
2023-09-06
phs003413 Immune Responses in Checkpoint Myocarditis Across Heart, Blood, and Tumor Case-Control
2023-09-07
phs003415 Resistance Development in Basal Cell Nevus Syndrome through the Basal to Squamous Transition Case Set
2023-09-07
phs003416 Transcriptomic and Epigenetic Profiling of SCLC Patient Samples Epigenetics
2023-09-10
phs003417 The Chromatin Landscape of Pathogenic Transcriptional Cell States in Rheumatoid Arthritis Case Set
2023-09-11
phs003418 Altered Interactions between Circulating and Tissue-Resident CD8 T Cells with the Colonic Mucosa Define Checkpoint Inhibitor Colitis Case-Control
2023-09-12
phs003421 Joint Addiction, Aging, and Mental Health Data Access Committee General Research Use Datasets (GSR Restricted) Collection None
2023-09-17
phs003422 Hereditary Gastric Cancer Syndromes: An Integrated Genomic and Clinicopathologic Study of the Predisposition to Gastric Cancer Case Set
2023-09-18
phs003427 Single-Cell Profiling of Premature Neonate Airways Reveals a Continuum of Myeloid Differentiation Single Cell Analysis
2023-09-24
phs003428 CALGB/SWOG 80405: Genome-Wide Association Study of Patients with Advanced or Metastatic Colorectal Cancer Treated with First-Line Chemotherapy Combined with Cetuximab and/or Bevacizumab eQTL
2023-09-25
phs003429 Whole-Exome Sequencing Study of Diabetic Nephropathy Case-Control
2023-09-26
phs003432 Childhood Cancer Data Initiative (CCDI): Identification and Targeting of Treatment Resistant Progenitor Populations in T-cell Acute Lymphoblastic Leukemia Single Cell Analysis
2023-10-01
phs003435 Circulating Genomic Determinants of Treatment Failure in Hodgkin Lymphoma Case-Control
2023-10-02
phs003436 KRT17High/CXCL8+ Tumor Cells Display Both Classical and Basal Features and Regulate Myeloid Infiltration in the Pancreatic Cancer Microenvironment Observational
2023-10-03
phs003437 Basal-to-Inflammatory Transition Contributes to Basal Cell Carcinoma Therapy Resistance via Crosstalk with a Pro-Inflammatory Stromal Niche Case Set
2023-10-03
phs003442 Early Family Prevention of Adolescent Alcohol, Drug Use, and Psychopathology Cross-Sectional
2023-10-09
phs003444 The Cancer Dependency Map (DepMap) Collection
2023-10-12
phs003446 Profiling RNA Translation in Pediatric Medulloblastoma RNA Sequencing
2023-10-15
phs003447 MAESTRO-Pool Enables Highly Parallel and Specific Mutation-Enrichment Sequencing for Minimal Residual Disease Detection in Cohort Studies Case Set
2023-10-15
phs003448 Non-Coding Autoimmune Risk Variant Defines Role for ICOS in T Peripheral Helper Cell Development Cross-Sectional
2023-10-16
phs003451 The Genetic Evolution of Acral Melanoma Exome Sequencing
2023-10-16
phs003452 Phase 2 Study of Pembrolizumab in Combination with Gemcitabine and Cisplatin as Neoadjuvant Therapy Case Set
2023-10-18
phs003453 Investigating Genetics in Suspected Congenital Syndromes Case Set
2023-10-18
phs003455 Correlative Studies for Protocol #14-C-0059: T Cells Expressing an Anti-GD2 Chimeric Antigen Receptor in Patients with GD2+ Solid Tumors, a Collaboration with CIMAC-CIDC Clinical Cohort
2023-10-24
phs003458 Mapping Disease Pathways for Biliary Atresia Case Set
2023-10-26
phs003460 Blood Transcriptome Profiling Following Seizures Case-Control
2023-10-29
phs003462 Tumor detection by analysis of both symmetric- and hemi-methylation of plasma cell-free DNA Case-Control
2023-10-30
phs003463 NIH RECOVER: A Multi-Site Observational Study of Post-Acute Sequelae of SARS-CoV-2 Infection in Adults Longitudinal Cohort
2023-10-30
phs003466 Breast Cancer in Blacks: Impact of Genomics, Healthcare Use and Lifestyle on Outcomes (BRIGHT) Individual-Level Genomic Data
2023-11-02
phs003468 The Role of GPD1L in the Pathogenesis of Brugada Syndrome Exome Sequencing
2023-11-05
phs003469 Genetic Markers of Lipids in Indians: A Validation Study of Most Relevant Findings of Genome-Wide Association Studies Cross-Sectional
2023-11-06
phs003470 Unrelated Donor Reduced Intensity Bone Marrow Transplant for Children with Severe Sickle Cell Disease (BMT CTN-0601-BioLINCC) Clinical Trial
2023-11-06
phs003473 Cellular and Molecular Investigations of Human Hearts Control Set
2023-11-13
phs003474 A Missense SNP in the Tumor Suppressor SETD2 Reduces H3K36me3 and Mitotic Spindle Integrity in Drosophila Case-Control
2023-11-15
phs003475 PIEZO1 Loss of Function Compound Heterozygous Mutation in the Rare Congenital Human Disorder Prune Belly Syndrome Exome Sequencing
2023-11-15
phs003477 BPH Tissues for Cell Culture and Analysis - Spatial Transcriptomics Identifies Candidate Stromal Drivers of Benign Prostatic Hyperplasia Case Set
2023-11-20
phs003480 Single-Cell RNA-Sequencing of Human Prostatectomy Tissue Single Cell Analysis
2023-11-29
phs003483 Systolic Blood Pressure Intervention Trial (SPRINT-BioLINCC) Clinical Trial
2023-12-01
phs003485 Germline Genome Sequencing from Patients with Early-Onset Merkel Cell Carcinoma Whole Genome Sequencing
2023-12-04
phs003486 Acquired Cross-Resistance in Small Cell Lung Cancer Patient-Derived Xenografts Xenograft
2023-12-05
phs003488 APOLLO-OV: Applied Proteogenomics of High Grade Serous Ovarian Carcinoma Tumor
2023-12-06
phs003489 FLG LoF Variants are Associated with Atopic Dermatitis in an Early-Life Prospective Cohort Case Set
2023-12-06
phs003495 Postmortem Analysis of the Caudate Nucleus in Schizophrenia Case-Control
2023-12-11
phs003496 Utility of Capillary Blood in Gene Expression Studies Methods Development
2023-12-11
phs003497 Combinatorial Indexed 10x Genomics Single-Cell ATAC-seq on Human Cerebral Cortex Control Set
2023-12-13
phs003501 Systems Analysis of Single-Cell Heterogeneity Underlying Glioma Drug Resistance Case Set
2023-12-18
phs003502 Single-Cell and Spatial Multi-Omics Highlight Effects of Anti-Integrin Therapy Across Cellular Compartments in Ulcerative Colitis Case-Control
2023-12-18
phs003503 ILyAD (Indolent Lymphoma And vitamin D) Clinical Trial
2023-12-19
phs003506 Heart Failure Network Aldosterone Targeted Neurohormonal Combined with Natriuresis Therapy - (HFN ATHENA-BioLINCC) Clinical Trial
2023-12-19
phs003509 Protracted Neuronal Recruitment in the Temporal Lobe of Young Children Control Set
2023-12-25
phs003510 Heart Failure Network - Effectiveness of Ultrafiltration in Treating People with Acute Decompensated Heart Failure and Cardiorenal Syndrome (HFN CARRESS - BioLINCC) Clinical Trial
2023-12-27
phs003511 Direct Transposition of Native DNA for Sensitive Multimodal Single-Molecule Sequencing Methods Development
2023-12-27
phs003512 Identification of Host Genetic Factors That Are Determinant for the Development of Severe Forms of COVID-19 Case Set
2023-12-28
phs003519 Childhood Cancer Data Initiative (CCDI): Single-Cell Atlas of NF1 Nerve Sheath Tumors Longitudinal
2024-01-07
phs003521 Cell Type-Specific and Disease-Associated eQTL in the Human Lung Case-Control
2024-01-08
phs003522 Epigenetic Damage in Women Living in LA Food-Desert Zip Codes Case Set
2024-01-09
phs003524 Heart Failure Network: Diuretic Optimization Strategies Evaluation in Acute Heart Failure (HFN DOSE-BioLINCC) Clinical Trial
2024-01-15
phs003529 Sickle Cell Disease Natural History Data Resource (SCD NHDR) Clinical Cohort
2024-01-18
phs003531 A Prospective Study of Lifestyle, the Gut Microbiome, and Diverticulitis Case-Control
2024-01-19
phs003532 Cellular Heterogeneity in Early Human Development at Stage CS16 Sequencing
2024-01-21
phs003533 Heart Failure Network - Xanthine Oxidase Inhibition for Hyperuricemic Heart Failure Patients (HFN EXACT-BioLINCC) Clinical Trial
2024-01-23
phs003535 Integrating Genomic and Transcriptomic Data to Identify Breast Cancer Susceptibility Genes Genotype
2024-01-25
phs003537 HudsonAlpha Long Read Sequencing Data of Individuals with Rare Suspected Genetic Conditions Case Set
2024-01-28
phs003538 Light at Night and Prostate Cancer in the Health Professionals Follow-Up Study Longitudinal
2024-02-01
phs003541 Identification of Novel Therapeutic Targets for Calcific Aortic Valve Stenosis Using Integrative Genomics RNA Sequencing
2024-02-04
phs003542 Heart Failure Network: Functional Impact of GLP-1 for Heart Failure Treatment (HFN FIGHT-BioLINCC) Clinical Trial
2024-02-05
phs003543 National Sleep Research Resource (NSRR): Hispanic Community Health Study/Study of Latinos Cohort
2024-02-05
phs003546 Gene Expression and Biomarker Utility in Post-Mortem Samples Methods Development
2024-02-06
phs003550 The Genetics of Food Cue Reactivity in Children Clinical Trial
2024-02-08
phs003551 Action to Control Cardiovascular Risk in Diabetes (ACCORD-BioLINCC) Clinical Trial
2024-02-10
phs003557 Heart Failure Network Oral Iron Repletion Effects on Oxygen Uptake in Heart Failure (HFN IRONOUT-BioLINCC) Clinical Trial
2024-02-14
phs003561 Spatial Transcriptomics Reveals Discrete Tumor Microenvironments and Autocrine Loops Within Ovarian Cancer Subclones Tumor
2024-02-20
phs003562 Action to Control Cardiovascular Risk in Diabetes (ACCORD - Imaging) Clinical Trial
2024-02-21
phs003563 Transfer Learning Associates CAFs with EMT and Inflammation in Tumor Cells in Human Tumors and Organoid Co-Culture in Pancreatic Ductal Adenocarcinoma Cohort
2024-02-21
phs003564 Nasal MicroRNA during Bronchiolitis and Age 6y Asthma: MARC-35 Cohort Longitudinal Cohort
2024-02-21
phs003566 Systolic Blood Pressure Intervention Trial (SPRINT-Imaging) Clinical Trial
2024-02-21
phs003567 Association Between Telomere Length and Falciparum Malaria Endemicity in Sub-Saharan Africans Cohort
2024-02-22
phs003569 Aberrant Activation of Wound Healing Programs within the Metastatic Niche Facilitates Lung Colonization by Osteosarcoma Cells Case Set
2024-02-26
phs003570 Detecting and Subtyping Lung Cancer Through Analysis of Circulating Tumor DNA Case-Control
2024-02-27
phs003574 Adult Eosinophilic Esophagitis Registry Atlas Case-Control
2024-03-03
phs003578 REDS-IV-P Epidemiology, Surveillance and Preparedness of the Novel SARS-CoV-2 Epidemic (RESPONSE) Cohort
2024-03-05
phs003579 Phase II Study of Cryoablation and Post-Progression Immune Checkpoint Inhibition in Metastatic Melanoma Case Set
2024-03-05
phs003581 Genetic and Genomic Analysis of Primary Human Chondrocytes Case-Cohort
2024-03-06
phs003582 Regulation of T Cell CXCL13 Production Case Set
2024-03-07
phs003586 Luminal Androgen Receptor-Enriched Triple Negative Breast Cancer Case Set
2024-03-11
phs003587 Laser Capture Microscopy (LCM)-RNAseq for Topological Mapping of Synovial Pathology during Rheumatoid Arthritis Case-Control
2024-03-11
phs003589 Heart Failure Network - Renal Optimization Strategies Evaluation in Acute Heart Failure and Reliable Evaluation of Dyspnea (HFN ROSE-BioLINCC) Clinical Trial
2024-03-17
phs003590 FIGHT-207: Anonymized Genomic Alterations and Clinical Responses Interventional
2024-03-18
phs003593 Framingham Heart Study-Cohort (FHS-Cohort) - Imaging Longitudinal
2024-03-26
phs003599 Heart Failure: A Controlled Trial Investigating Outcomes of Exercise Training (HF-ACTION-BioLINCC) Clinical Trial
2024-04-01
phs003600 Comprehensive Genomic Data Deposition for Pancreatic Cancer Precision Medicine Studies: Clinical Trials NCT02451982 and NCT02648282 Clinical Cohort
2024-04-01
phs003601 Transcriptomic Profiling of Peripheral Immune Cells in a Trial of Ruxolitinib with Nivolumab for Anti-PD1 Non-Responsive cHL Case Set
2024-04-01
phs003604 HiDEF-seq Single-Molecule Sequencing of Single-Strand Mismatches and Damage Sequencing
2024-04-08
phs003607 Type I Interferon Exacerbates Mycobacterium Tuberculosis Induced Human Macrophage Death RNA Sequencing
2024-04-09
phs003613 Chromatin Landscape of BET Inhibitor-Treated CD8+ T-cells from Chronic Lymphocytic Leukemia Patients Aggregate Genomic Data
2024-04-16
phs003615 Phase 2 Study of Nivolumab and Entinostat in Unresectable or Metastatic Cholangiocarcinoma and Pancreatic Adenocarcinoma Clinical Cohort
2024-04-18
phs003619 Environmental Influences on Child Health Outcomes (ECHO) - PATHWAYS - Conditions Affecting Neurocognitive Development and Learning in Early Childhood (CANDLE) Genotype/Expression
2024-04-21
phs003620 Environmental Influences on Child Health Outcomes (ECHO) - PATHWAYS - Global Alliance to Prevent Prematurity and Stillbirth (GAPPS) Genotype/Expression
2024-04-21
phs003621 Guiding Evidence Based Therapy Using Biomarker Intensified Treatment in Heart Failure (GUIDE-IT-BioLINCC) Clinical Trial
2024-04-22
phs003623 BIRC5 Upregulation Enhances DNMT3A-Mutant T-ALL Cell Survival and Pathogenesis Case Set
2024-04-24
phs003629 Pre-Existing Skin-Resident CD8 and γδ T Cell Circuits Mediate Immune Response in Merkel Cell Carcinoma and Predict Immunotherapy Efficacy Case Set
2024-04-30
phs003633 Joint-Specific TF Regulation in RA Case Set
2024-05-06
phs003634 Genomic Analysis of Diffuse Large B Cell Lymphoma Case Set
2024-05-06
phs003637 Sleep Heart Health Study (SHHS-BioLINCC) Observational
2024-05-09
phs003639 Cardiovascular Health Study (CHS) - Imaging Cohort
2024-05-13
phs003640 The Somatic Mutational Landscape of Thyroid Cancer in Patients with Germline PTEN Mutations Case-Control
2024-05-16
phs003644 Left Atrial Cardiomyocyte Transcriptomic Analysis of Postoperative Atrial Fibrillation Cohort
2024-05-19
phs003645 Single Cell Analysis of Healthy and Diseased Temporomandibular Joint Synovial Fluid Methods Development
2024-05-20
phs003647 Genetic Investigations of Attention-Deficit/Hyperactivity Disorder Case-Control
2024-05-20
phs003651 NHLBI TOPMed: MWCCS: Sex Differences in the Role of Multi-Omics in HIV-Associated Carotid Artery Atherosclerosis Longitudinal Cohort
2024-05-22
phs003654 Sudden Cardiac Death in Heart Failure Trial (SCD-HeFT-BioLINCC) Clinical Trial
2024-05-22
phs003657 The Effects of Long-Term Heavy Metal Exposure on Transcriptome Landscape in Human Peripheral Blood Cells Case-Control
2024-05-28
phs003659 Exome Sequencing of Alcohol-Associated Hepatitis Case-Control
2024-05-28
phs003665 Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist (TOPCAT-BioLINCC) Clinical Trial
2024-06-02
phs003666 Rapid Acceleration of Diagnostics - Digital Health Technologies' (RADx-DHT) Collection of General Research Use Datasets Case Set
2024-06-03
phs003667 Heart Failure Network: Inorganic Nitrite Delivery to Improve Exercise Capacity in HFpEF (HFN INDIE-BioLINCC) Clinical Trial
2024-06-04
phs003668 Studies of Left Ventricular Dysfunction (SOLVD-BioLINCC) Clinical Trial
2024-06-04
phs003674 Integrative Gene Regulatory Network Analysis Discloses Key Driver Genes of Fibromuscular Dysplasia Cohort
2024-06-09
phs003676 Chromothripsis in Small Cell Lung Carcinoma Associated with Carcinoid Transformation Case Set
2024-06-11
phs003678 INCLUDE Data Hub: NDA GUIDs for Down Syndrome Research Cohort
2024-06-13
phs003679 High-Fidelity, Large-Scale Targeted Profiling of Microsatellites Parent-Offspring Trios
2024-06-13
phs003682 EWS-WT1 Fusion Isoforms Establish Oncogenic Programs and Therapeutic Vulnerabilities in Desmoplastic Small Round Cell Tumors Case Set
2024-06-17
phs003683 Somatic Mutations in Individual Skin Cells Cross-Sectional
2024-06-17
phs003697 Evolving Cell States and Oncogenic Drivers during the Progression of IDH-Mutant Gliomas Case-Cohort
2024-06-26
phs003700 Analyzing Somatic Mutagenesis in Systemic Sclerosis Case-Control
2024-07-01
phs003701 A Collaborative Search for New Genes for Non-Syndromic Deafness Parent-Offspring
2024-07-01
phs003702 Multi-Ethnic Study of Atherosclerosis (Echocardiogram Image Repository) Cohort
2024-07-01
phs003703 Multi-Ethnic Study of Atherosclerosis (Electrocardiogram Tracing Repository) Cohort
2024-07-01
phs003704 Botensilimab, an Fc-enhanced Anti-CTLA-4 Antibody, is Effective Against Tumors Poorly Responsive to Conventional Immunotherapy Clinical Trial
2024-07-03
phs003706 Clinical Outcomes and ctDNA Correlates for CAPOX BETR: A phase II trial of Capecitabine, Oxaliplatin, Bevacizumab, Trastuzumab in Previously Untreated Advanced HER2+ Gastroesophageal Adenocarcinoma Clinical Trial
2024-07-08
phs003712 Early Detection of Malignant and Pre-Malignant Peripheral Nerve Tumors Using Cell-Free DNA Fragmentomics Case-Control
2024-07-15
phs003713 Transcription Factor Analysis of SLE Case-Control
2024-07-16
phs003717 Molecular Analysis of Alliance A031201 Study Case Set
2024-07-21
phs003746 The Contribution of De Novo Coding Mutations to Meningomyelocele Parent-Offspring Trios
2024-08-15
