Variant calling on GRCh38 with the 1000 genomes samples

ABSTRACT: 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.

INSTRUMENT(S): -

ORGANISM(S): Homo Sapiens

SUBMITTER: EMBL-EBI 

PROVIDER: PRJEB30460 | EVA | 2018-12-19

REPOSITORIES: EVA