.\" DO NOT MODIFY THIS FILE! It was generated by help2man 1.41.1. .TH VCF-CONTRAST "1" "February 2013" "vcf-contrast" "User Commands" .SH NAME vcf-contrast \- finds differences amongst samples .SH SYNOPSIS .B vcf-contrast \fI+ - \fR[\fIOPTIONS\fR] \fIfile.vcf.gz\fR .SH DESCRIPTION About: Finds differences amongst samples adding NOVEL* annotation to INFO field. .SH OPTIONS .TP + List of samples where unique variant is expected .TP \- List of background samples .TP \fB\-d\fR, \fB\-\-min\-DP\fR Minimum depth across all \- samples .TP \fB\-f\fR, \fB\-\-apply\-filters\fR Skip sites with FILTER column different from PASS or "." .TP \fB\-n\fR, \fB\-\-novel\-sites\fR Print only records with novel genotypes .TP \fB\-h\fR, \-?, \fB\-\-help\fR This help message. .SS "Example:" .IP # Test if any of the samples A,B is different from all C,D,E vcf\-contrast +A,B \fB\-C\fR,D,E \fB\-m\fR file.vcf.gz .IP # Same as above but printing only sites with novel variants and table output vcf\-contrast \fB\-n\fR +A,B \fB\-C\fR,D,E \fB\-m\fR file.vcf.gz | vcf\-query \fB\-f\fR '%CHROM %POS\et%INFO/NOVELTY\et%INFO/NOVELAL\et%INFO/NOVELGT[\et%SAMPLE %GTR %PL]\en' .IP # Similar to above but require minimum mapping quality of 20 vcf\-annotate \fB\-f\fR MinMQ=20 file.vcf.gz | vcf\-contrast +A,B,C \fB\-D\fR,E,F \fB\-f\fR .IP