shallow coverage whole genome sequencing

Dr Xiaolong Fan
xfan@bnu.edu.cn

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Dataset ID	Description	Technology	Samples
EGAD00001005062	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.		147