Study Detail

TitleVariant calling on GRCh38 with the 1000 genomes samples 2
Study TypeOther
Abstract We present biallelic SNVs+INDELs 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 .. [more]
Description We present biallelic SNVs+INDELs 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 .. [more]
Center NameEMBL-EBI