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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