'\" t .\" Title: gt-seqmutate .\" Author: [FIXME: author] [see http://www.docbook.org/tdg5/en/html/author] .\" Generator: DocBook XSL Stylesheets vsnapshot .\" Date: 07/22/2020 .\" Manual: GenomeTools Manual .\" Source: GenomeTools 1.6.1 .\" Language: English .\" .TH "GT\-SEQMUTATE" "1" "07/22/2020" "GenomeTools 1\&.6\&.1" "GenomeTools Manual" .\" ----------------------------------------------------------------- .\" * Define some portability stuff .\" ----------------------------------------------------------------- .\" ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ .\" http://bugs.debian.org/507673 .\" http://lists.gnu.org/archive/html/groff/2009-02/msg00013.html .\" ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ .ie \n(.g .ds Aq \(aq .el .ds Aq ' .\" ----------------------------------------------------------------- .\" * set default formatting .\" ----------------------------------------------------------------- .\" disable hyphenation .nh .\" disable justification (adjust text to left margin only) .ad l .\" ----------------------------------------------------------------- .\" * MAIN CONTENT STARTS HERE * .\" ----------------------------------------------------------------- .SH "NAME" gt-seqmutate \- Mutate the sequences of the given sequence file(s)\&. .SH "SYNOPSIS" .sp \fBgt seqmutate\fR [option \&...] [sequence_file \&...] .SH "DESCRIPTION" .PP \fB\-rate\fR [\fIvalue\fR] .RS 4 set the mutation rate (default: 1) .RE .PP \fB\-width\fR [\fIvalue\fR] .RS 4 set output width for FASTA sequence printing (0 disables formatting) (default: 0) .RE .PP \fB\-o\fR [\fIfilename\fR] .RS 4 redirect output to specified file (default: undefined) .RE .PP \fB\-gzip\fR [\fIyes|no\fR] .RS 4 write gzip compressed output file (default: no) .RE .PP \fB\-bzip2\fR [\fIyes|no\fR] .RS 4 write bzip2 compressed output file (default: no) .RE .PP \fB\-force\fR [\fIyes|no\fR] .RS 4 force writing to output file (default: no) .RE .PP \fB\-help\fR .RS 4 display help and exit .RE .PP \fB\-version\fR .RS 4 display version information and exit .RE .sp For each position in the given sequences it is randomly determined with probability (mutation rate / 100) if the given position is mutated\&. If so, in 80% of the cases a substitution is performed, in 10% an insertion, and in 10% a deletion, respectively\&. For substitution and insertion events, the nucleotide is generated randomly without regard to the original nucleotide\&. That is, resubstitutions are possible\&. This procedure equals the one described on page 1867 of the following paper: .sp \fIT\&.D\&. Wu and C\&.K\&. Watanabe\&. GMAP: a genomic mapping and alignment program for mRNA and EST sequences\&. Bioinformatics, 21(9):1859\-1875, 2005\&.\fR .SH "REPORTING BUGS" .sp Report bugs to https://github\&.com/genometools/genometools/issues\&.