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ggd-genomics / packages / grch38-exome-variants-gnomad-v1 1

SNV and INDEL varaints from 125,748 exomes in the gnomAD dataset version 2.1.1 in bcf format. These variants were lifted over from gnomAD v2.1.1 GRCh37 to GRCh38 by the gnomAD group. The file constains all subsets of non-neuro, non-cancer, controls-only, and non-TOPMed samples.

  • 21 total downloads
  • Last upload: 4 years and 10 months ago

Installers

  • noarch v1

conda install

To install this package run one of the following:
conda install ggd-genomics::grch38-exome-variants-gnomad-v1

Description


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