Hi,I'm new here.
I'm going to do rare variant analysis(CAST CMC)
now I have a vcf file(only snp) which contains case and control group
but there are too many positions
are there any way to make them as gene set like MAP4,FLNB,ABTB1
forgive me for my poor english,thx
I'm going to do rare variant analysis(CAST CMC)
now I have a vcf file(only snp) which contains case and control group
but there are too many positions
are there any way to make them as gene set like MAP4,FLNB,ABTB1
forgive me for my poor english,thx
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