Mercurial > repos > big-tiandm > mirplant2
changeset 27:eaf9715e5143 draft
Uploaded
author | big-tiandm |
---|---|
date | Thu, 31 Jul 2014 03:04:27 -0400 |
parents | c90e7d84d521 |
children | 5e05c9bb919c |
files | convert_bowtie_to_blast.pl |
diffstat | 1 files changed, 126 insertions(+), 0 deletions(-) [+] |
line wrap: on
line diff
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/convert_bowtie_to_blast.pl Thu Jul 31 03:04:27 2014 -0400 @@ -0,0 +1,126 @@ +#!/usr/bin/perl + + +use warnings; +use strict; +use Getopt::Std; + +######################################### USAGE ################################ + +my $usage= +"$0 file_bowtie_result file_solexa_seq file_chromosome + +This is a converter which changes Bowtie output into Blast format. +The input includes three files: a Bowtie result file (default Bowtie +output file), a fasta file consisting of small Reads and a chromosome +fasta file. It outputs the alignments in blast_parsed format. + +file_bowtie_result likes: + +AtFlower100010_x2 + MIR319c 508 AAGGAGATTCTTTCAGTCCAG IIIIIIIIIIIIIIIIIIIII 0 +AtFlower1000188_x1 + MIR2933a 421 TCGGAGAGGAAATTCGTCGGCG IIIIIIIIIIIIIIIIIIIIII 0 + +file_solexa_seq likes: + +>AtFlower100010_x2 +AAGGAGATTCTTTCAGTCCAG + +file_chromosome contains chromosome seq in fasta format + +"; + + +####################################### INPUT FILES ############################ + +my $file_bowtie_result=shift or die $usage; +my $file_short_seq=shift or die $usage; +my $file_chromosome_seq=shift or die $usage; + + +##################################### GLOBAL VARIBALES ######################### + +my %short_seq_length=(); +my %chromosome_length=(); + + +######################################### MAIN ################################# + +#get the short sequence id and its length +sequence_length($file_short_seq,\%short_seq_length); + +#get the chromosome sequence id and its length +sequence_length($file_chromosome_seq,\%chromosome_length); + +#convert bowtie result format to blast format; +change_format($file_bowtie_result); + +exit; + + +##################################### SUBROUTINES ############################## + +sub sequence_length{ + my ($file,$hash) = @_; + my ($id, $desc, $sequence, $seq_length) = (); + + open (FASTA, "<$file") or die "can not open $$file\n"; + while (<FASTA>) + { + chomp; + if (/^>(\S+)(.*)/) + { + $id = $1; + $desc = $2; + $sequence = ""; + while (<FASTA>){ + chomp; + if (/^>(\S+)(.*)/){ + $$hash{$id} = length $sequence; + $id = $1; + $desc = $2; + $sequence = ""; + next; + } + $sequence .= $_; + } + } + } + $seq_length=length($sequence); + $$hash{$id} = $seq_length; + close FASTA; +} + + + + + +sub change_format{ + #Change Bowtie format into blast format + my $file=shift @_; + open(FILE,"<$file")||die"can not open the bowtie result file:$!\n"; + #open(BLASTOUT,">blastout")||die"can not create the blastout file:$!\n"; + + while(<FILE>){ + chomp; + my @tmp=split("\t",$_); + #Clean the reads ID + my @tmp1=split(" ",$tmp[0]); + print "$tmp1[0]"."\t"."$short_seq_length{$tmp1[0]}"."\t"."1".'..'."$short_seq_length{$tmp1[0]}"."\t"."$tmp[2]"."\t"."$chromosome_length{$tmp[2]}"."\t"; + if($tmp[1] eq "+"){ + my $seq_end=$tmp[3] + $short_seq_length{$tmp1[0]}; + my $seq_bg=$tmp[3] + 1; + print "$seq_bg".'..'."$seq_end"."\t"."1e-04"."\t"."1.00"."\t"."42.1"."\t"."Plus / Plus"."\n"; + } + if($tmp[1] eq "-"){ + my $seq_end=$chromosome_length{$tmp[2]} - $tmp[3]; + my $seq_bg=$seq_end - $short_seq_length{$tmp1[0]} + 1; + print "$seq_bg".'..'."$seq_end"."\t"."1e-04"."\t"."1.00"."\t"."42.1"."\t"."Plus / Minus"."\n"; + } + } + +# close BLASTOUT; + +} + + +