Whole genome sequencing of pediatric BCR-ABL1 positive acute lymphoblastic leukemia
We performed whole-genome sequencing of 18 paired tumor/normal BCR-ABL1+ leukemia genomes and analyzed single nucleotide variations (SNVs), insertion/deletions, structural variations and copy number variations in the tumor and normal genomes
- Type: Whole Genome Sequencing
- Archiver: European Genome-Phenome Archive (EGA)
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
| Dataset ID | Description | Technology | Samples | 
|---|---|---|---|
| EGAD00001000163 | Illumina HiSeq 2000 | 18 | |
| EGAD00001001432 | Illumina HiSeq 2000 | 1337 | |
| EGAD00001001433 | Illumina HiSeq 2000 | 906 | 
| Publications | Citations | 
|---|---|
| Germline ETV6 Mutations Confer Susceptibility to Acute Lymphoblastic Leukemia and Thrombocytopenia. PLoS Genet 11: 2015 e1005262 | 74 | 
| The landscape of coding RNA editing events in pediatric cancer. BMC Cancer 21: 2021 1233 | 6 | 
| Comprehensive analysis of mutational signatures reveals distinct patterns and molecular processes across 27 pediatric cancers. Nat Cancer 4: 2023 276-289 | 13 | 
