Variant calling on GRCh38 with the 1000 genomes samples
收藏NIAID Data Ecosystem2026-03-10 收录
下载链接：
https://www.omicsdi.org/dataset/eva/PRJEB30460
下载链接
链接失效反馈官方服务：
资源简介：
We present biallelic SNVs called from 2,548 samples across 26 populations from the 1000 Genomes Project, called directly against GRCh38. We believe this will be a useful reference resource for those working on GRCh38, representing an improvement over the “lift-overs” of 1000 Genomes data that have been available to date and providing a resource necessary for the full adoption of GRCh38 by the community.
创建时间：
2018-12-19
