Entering edit mode
2.4 years ago
ThunderPhoenix
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0
Hello! So, lets say I have a sorted, indexed (tabix) VCF file, and wanted to make a new subsetted VCF file out of the that contains only a specific region from chr1. In that case, I know that tabix chr1.vcf.gz:<start>-<end>
will give you the raw subsetted genotype data. How do I create a valid VCF file out of this? Thanks!
Actually I just used bcftools view and subset the specified chromosome. I'd imagine subsetting via vcftools would be equivalently good.
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