Whole genome SNP array data from myelodysplastic syndromes (MDS) patients
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE57229
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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.
创建时间:
2014-06-02



