Whole genome sequencing of pediatric BCR-ABL1 positive acute lymphoblastic leukemia

Study

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 DATA FILES FOR SJPHALL	Illumina HiSeq 2000	18
EGAD00001001432	PCGP Germline Study Whole Genome Sequencing PCGP Germline Study Whole Genome Sequencing	Illumina HiSeq 2000	1337
EGAD00001001433	PCGP Germline Study Whole Exome Sequencing PCGP Germline Study Whole Exome Sequencing	Illumina HiSeq 2000	906

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