Transcriptomics

Dataset Information

32

Whole genome SNP array data from myelodysplastic syndromes (MDS) patients


ABSTRACT: With the whole genome SNP array information obtained from tumor and matched normal control, we could evaluate the acquired copy number variations (CNVs) and uniparental disomies (UPDs) . Seven MDS patients in a whole genome sequencing project were included in this experiment. To detect acquired CNVs and UPDs in MDS patients, we genotyped both CD34+ cell from bone marrow and matched skin tissue.

ORGANISM(S): Homo sapiens  

SUBMITTER: Zhaohui Gu  Saijuan Chen   Zhu Chen    

PROVIDER: E-GEOD-57229 | ArrayExpress| 2014-06-03

SECONDARY ACCESSION(S): GSE57229PRJNA246092

REPOSITORIES: GEO, ArrayExpress

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