grch37-exome-variants-gnomad-v1
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.
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.
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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
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24
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