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grch37-exome-variants-gnomad-v1

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SNV and INDEL varaints from 125,748 exomes in the gnomAD dataset version 2.1.1 in bcf format. The file constains all subsets of non-neuro, non-cancer, controls-only, and non-TOPMed samples.

Installation

To install this package, run one of the following:

Conda
$conda install ggd-genomics::grch37-exome-variants-gnomad-v1

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Summary

SNV and INDEL varaints from 125,748 exomes in the gnomAD dataset version 2.1.1 in bcf format. The file constains all subsets of non-neuro, non-cancer, controls-only, and non-TOPMed samples.

Last Updated

Oct 2, 2020 at 15:52

Total Downloads

24

Supported Platforms

noarch