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we use it in exome, in the filter_vcf step, but the gnomad vcf we're using is only a subset, restricted to exome coords. Would be nice to revisit that decision at some point (options: leave it out, apply it to exome only, or find a new genome-wide VCF)
The text was updated successfully, but these errors were encountered:
we use it in exome, in the filter_vcf step, but the gnomad vcf we're using is only a subset, restricted to exome coords. Would be nice to revisit that decision at some point (options: leave it out, apply it to exome only, or find a new genome-wide VCF)
The text was updated successfully, but these errors were encountered: