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 |
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Germline ETV6 Mutations Confer Susceptibility to Acute Lymphoblastic Leukemia and Thrombocytopenia.
PLoS Genet 11: 2015 e1005262 |
75 |
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 |
15 |