Mercurial > repos > xuebing > sharplabtool
view tools/human_genome_variation/mergeSnps.pl @ 1:cdcb0ce84a1b
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author | xuebing |
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date | Fri, 09 Mar 2012 19:45:15 -0500 |
parents | 9071e359b9a3 |
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#!/usr/bin/env perl use strict; use warnings; #this merges the significance output with the SNPs so users get more than an index my($out, $snp) = @ARGV; if (!$out or !$snp) { die "missing args\n"; } #merge SNP data with results merge(); exit; ######################################## #merge the input and output files so have SNP data with result sub merge { open(FH, $out) or die "Couldn't open $out, $!\n"; my %res; my @ind; while (<FH>) { chomp; my $line = $_; #0: 10 score= 14.224153 , df= 2 , p= 0.040760 , N=50 if ($line =~ /^(\d+):\s+(.*)/) { $res{$1} = $2; push(@ind, $1); } } close FH; if (!@ind) { return; } #no results, leave alone @ind = sort { $a <=> $b } @ind; #read input file to get SNP data open(FH, $snp) or die "Couldn't open $snp, $!\n"; my $i = 0; #0 based, not counting ID line my $c = shift @ind; while (<FH>) { chomp; if (/^ID/) { next; } my @f = split(/\s+/); if ($i == $c) { $res{$i} = "$f[0]\t$f[1]\t$f[2]\t$res{$i}"; if (!@ind) { last; } $c = shift @ind; } $i++; } close FH; #now reprint results with SNP data included open(FH, ">", $out) or die "Couldn't write to $out, $!\n"; print FH "ID\tchr\tposition\tresults\n"; foreach $i (keys %res) { print FH $res{$i}, "\n"; } close FH; }