.\" Automatically generated by Pandoc 2.14.0.3 .\" .TH "WCFST" "1" "" "wcFst (vcflib)" "wcFst (VCF statistics)" .hy .SH NAME .PP \f[B]wcFst\f[R] .SH SYNOPSIS .PP \f[B]wcFst\f[R] \[en]target 0,1,2,3,4,5,6,7 \[en]background 11,12,13,16,17,19,22 \[en]file my.vcf \[en]deltaaf 0.1 \[en]type PL .SH DESCRIPTION .PP \f[B]wcFst\f[R] is Weir & Cockerham\[cq]s Fst for two populations. Negative values are VALID, they are sites which can be treated as zero Fst. For more information see Evolution, Vol. 38 N. 6 Nov 1984. Specifically \f[B]wcFst\f[R] uses equations 1,2,3,4. .SH OPTIONS .IP .nf \f[C] Output : 3 columns : 1. seqid 2. position 3. target allele frequency 4. background allele frequency 5. **wcFst** required: t,target -- argument: a zero based comma separated list of target individuals corrisponding to VCF columns required: b,background -- argument: a zero based comma separated list of background individuals corrisponding to VCF columns required: f,file -- argument: proper formatted VCF required, y,type -- argument: genotype likelihood format; genotype : GT,GL,PL,GP optional: r,region -- argument: a tabix compliant genomic range: seqid or seqid:start-end optional: d,deltaaf -- argument: skip sites where the difference in allele frequencies is less than deltaaf, default is zero Type: statistics \f[R] .fi .SH EXIT VALUES .TP \f[B]0\f[R] Success .TP \f[B]not 0\f[R] Failure .SH SEE ALSO .PP \f[B]vcflib\f[R](1) .SH OTHER .SH LICENSE .PP Copyright 2011-2023 (C) Erik Garrison and vcflib contributors. MIT licensed. .SH AUTHORS Erik Garrison and vcflib contributors.