.\" Automatically generated by Pandoc 2.14.0.3 .\" .TH "VCFNULLGENOFIELDS" "1" "" "vcfnullgenofields (vcflib)" "vcfnullgenofields (VCF transformation)" .hy .SH NAME .PP \f[B]vcfnullgenofields\f[R] .SH SYNOPSIS .PP \f[B]vcfnullgenofields\f[R] options .SH DESCRIPTION .PP Makes the FORMAT for each variant line the same (uses all the FORMAT fields described in the header). Fills out per-sample fields to match FORMAT. Expands GT values of `.' with number of alleles based on ploidy (eg: `./.' for dipolid). .SH OPTIONS .IP .nf \f[C] options: -p, --ploidy N the polidy of missing/null GT fields (default=2) -L, --expand_GL fill in missing GL fields with 0 values (eg: 0,0,0 for diploid 2 alleles) Type: transformation \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.