.\" Automatically generated by Pandoc 2.7.3 .\" .TH "GENOTYPESUMMARY" "1" "" "genotypeSummary (vcflib)" "genotypeSummary (VCF statistics)" .hy .SH NAME .PP \f[B]genotypeSummary\f[R] .SH SYNOPSIS .PP genotypeSummmary \[en]type PL \[en]target 0,1,2,3,4,5,6,7 \[en]file my.vcf \[en]snp .SH DESCRIPTION .PP Generates a table of genotype counts. Summarizes genotype counts for bi-allelic SNVs and indel .SH OPTIONS .IP .nf \f[C] output: table of genotype counts for each individual. required: t,target -- a zero based comma separated list of target individuals corresponding to VCF columns required: f,file -- proper formatted VCF required, y,type -- genotype likelihood format; genotype : GL,PL,GP optional, r,region -- a tabix compliant region : chr1:1-1000 or chr1 optional, s,snp -- Only count SNPs optional, a,ancestral -- describe counts relative to the ancestral allele defined as AA in INFO Type: statistics \f[R] .fi .SH EXIT VALUES .TP .B \f[B]0\f[R] Success .TP .B \f[B]not 0\f[R] Failure .SH SEE ALSO .PP \f[B]vcflib\f[R](1) .SH OTHER .SH LICENSE .PP Copyright 2011-2020 (C) Erik Garrison and vcflib contributors. MIT licensed. .SH AUTHORS Erik Garrison and vcflib contributors.