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 

PROVIDER: E-GEOD-57229 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress