Whole exome sequencing identifies centrosomal component gene mutations that increase human aneuploid conception risk, supplemental data
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https://rucore.libraries.rutgers.edu/rutgers-lib/61172
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资源简介：
This VCF file contains 162,365 SNVs identified across 160 individuals by whole exome sequencing that were used in the study. Allele counts (AC), total allele number (AN), and allele frequencies (AF) for either Low Aneuploidy Rate group (LRG) or High Aneuploidy Rateg group (HRG) were specified in the INFO tags.
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创建时间：
2019-08-23
