Normalization of whole-genome SNP data from non-Hodgkin lymphoma patients for copy number variation.
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE47357
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资源简介：
With the whole genome SNPs array information, we could evaluate the copy number variation of samples so as to find out specific DNA aberrations in non-Hodgkin lymphma comparing with reactive hyperplasia patients. To find out lymphoma-related copy number variations in 45 non-Hodgkin lymphoma patients comparing with 8 reactive hyperplasia patients.
创建时间：
2017-03-27
