bff38cab-b7f6-4d75-9517-0ba1c106bff3 - samples
收藏NIAID Data Ecosystem2026-03-11 收录
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资源简介：
We performed shallow coverage whole genome sequencing on 147 glioma samples and analyzed their copy number profile. The coverage of each sample is about 2. Data are presented as VCF files which describe the copy number segments and their log2 ratio.EGA dataset EGAD00001005062
创建时间：
2019-06-07
