Mercurial > repos > big-tiandm > sirna_plant
view matching.pl @ 26:80d514e98f72 draft
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author | big-tiandm |
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date | Thu, 06 Nov 2014 02:18:09 -0500 |
parents | 9dcffd531c76 |
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#!/usr/bin/perl -w #Filename: #Author: Tian Dongmei #Email: tiandm@big.ac.cn #Date: 2013/7/19 #Modified: #Description: my $version=1.00; use strict; use Getopt::Long; my %opts; GetOptions(\%opts,"i=s","g=s","index:s","v:i","p:i","r:s","o=s","h"); if (!(defined $opts{i} and defined $opts{o} ) || defined $opts{h}) { #necessary arguments &usage; } my $filein=$opts{'i'}; my $fileout=$opts{'o'}; unless ($fileout=~/\/$/) {$fileout.="/";} my $genome=$opts{'g'}; my $mis=defined $opts{'v'}? $opts{'v'} : 0; my $hits=defined $opts{'r'}? $opts{'r'} : 25; my $index=defined $opts{'index'} ? $opts{'index'} : ""; my $threads=defined $opts{'p'} ? $opts{'p'} : 1; #my $time=time(); #my $mapdir=$fileout."/genome_match_".$time; my $mapdir=$fileout."/genome_match"; mkdir $mapdir; chdir $mapdir; ###check genome index if (-s $index.".1.ebwt") { }else{ `bowtie-build $genome genome`; $index="genome"; } ### genome mapping `bowtie -v $mis -f -p $threads -m $hits -a --best --strata $index $filein --al genome_mapped.fa --un genome_not_mapped.fa > genome_mapped.bwt 2> run.log`; #`convert_bowtie_to_blast.pl genome_mapped.bwt genome_mapped.fa $genome > genome_mapped.bst`; sub usage{ print <<"USAGE"; Version $version Usage: $0 -i -o options: -i input file# input reads fasta/fastq file -g input file# genome file -index file-prefix #(must be indexed by bowtie-build) The parameter string must be the prefix of the bowtie index. For instance, if the first indexed file is called 'h_sapiens_37_asm.1.ebwt' then the prefix is 'h_sapiens_37_asm'.##can be null -v <int> report end-to-end hits w/ <=v mismatches; ignore qualities,default 0; -p/--threads <int> number of alignment threads to launch (default: 1) -r int a read is allowed to map up to this number of positions in the genome default is 25 -o output directory -h help USAGE exit(1); }