hum0331 Release Note
| Research ID | Release Date | Type of Data |
|---|---|---|
| hum0331.v1 | 2023/02/01 | Frequencies of variant information obtained from whole genome sequencing (WGS) analysis of 9850 participants without cancers or rare diseases |
hum0331.v1
WGS analysis of DNA samples from 9850 individuals registered in the NCBN biobank, which is available as a control for cancer and rare disease studies. Joint Call was performed together with the results of high coverage WGS analysis published by the International 1000 Genomes Project, and the allele frequency information for each population is provided in VCF.
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