Study
Whole genome sequencing of pediatric BCR-ABL1 positive acute lymphoblastic leukemia
Study ID | Alternative Stable ID | Type |
---|---|---|
EGAS00001000253 | Whole Genome Sequencing |
Study Description
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
Study Datasets 3 datasets.
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 |
DATA FILES FOR SJPHALL
|
Illumina HiSeq 2000 | 18 |
EGAD00001001432 |
PCGP Germline Study Whole Genome Sequencing
|
Illumina HiSeq 2000 | 1337 |
EGAD00001001433 |
PCGP Germline Study Whole Exome Sequencing
|
Illumina HiSeq 2000 | 906 |
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