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Thread | Thread Starter | Forum | Replies | Last Post |
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#1 |
Member
Location: USA Join Date: Oct 2012
Posts: 10
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Hello,
I would like to filter large multi-sample VCFs using allele frequencies obtained from VCFs or tab files from the EVS and 1000G datasets. I know that GATK and VCFtools can filter for allele freqs within a VCF, but they don't seem to offer a method to remove variants with a set frequency from an external source such as EVS or 1000G. Is there a tool/command to do this without having to create a list of variants from the databases and specifically remove them? Thanks |
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#2 |
Senior Member
Location: Amsterdam Join Date: Nov 2009
Posts: 112
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Tags |
1000 genomes project, bioinformactics, variant filtering, vcf, vcftools |
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