diff preProcess.pl @ 0:87fe81de0931 draft default tip

Uploaded

--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/preProcess.pl	Sun Jan 04 02:47:25 2015 -0500
@@ -0,0 +1,385 @@
+#!/usr/bin/perl -w
+#Filename:
+#Author: Tian Dongmei
+#Email: [e-mail]
+#Date: 2014-12-2
+#Modified:
+#Description: RNA-seq data pre-process
+my $version=1.00;
+
+use strict;
+use Getopt::Long;
+use threads;
+#use threads::shared;
+use File::Path;
+use File::Basename;
+#use RNA;
+#use Term::ANSIColor;
+
+my %opts;
+GetOptions(\%opts,"i:s@","tag:s@","format=s","phred:i","gfa=s","rfam:s","idx:s","idx2:s","mis:i","v:i","a:s","M:i","t:i","min:i","max:i","o:s","path:s","h");
+if (!(defined $opts{i} and defined $opts{format} and defined $opts{gfa} ) || defined $opts{h}) { #necessary arguments
+&usage;
+}
+
+my $time=&Time();
+print "miPlant program start:\n   The time is $time!\n";
+print "Command line:\n   $0 @ARGV\n";
+
+my $format=$opts{'format'};
+if ($format ne "fastq" && $format ne "fq" && $format ne "fasta" && $format ne "fa") { 
+	#&printErr();
+	die "Parameter \"-format\" is error! Parameter is fastq, fq, fasta or fa\n";
+}
+
+my $phred_qv=64;
+if (defined $opts{'phred'}) {$phred_qv=$opts{'phred'};}
+
+my @inputfiles=@{$opts{'i'}};
+my @inputtags=@{$opts{'tag'}};
+
+my  $mypath=`pwd`;
+chomp $mypath;
+
+my $dir=defined $opts{'o'} ? $opts{'o'} : "$mypath/preProcess/";
+
+
+unless ($dir=~/\/$/) {$dir.="/";}
+if (not -d $dir) {
+	mkdir $dir;
+}
+my $config=$dir."/input_config";
+open CONFIG,">$config";
+	for (my $i=0;$i<@inputfiles;$i++) {
+		print CONFIG $inputfiles[$i],"\t",$inputtags[$i],"\n";
+	}
+close CONFIG;
+
+my $scipt_path=defined $opts{'path'} ? $opts{'path'} : "/Users/big/galaxy-dist/tools/myTools/";
+
+my $a="ATCTCGTATG";  #adapter
+if (defined $opts{'a'}) {$a=$opts{'a'};}
+
+my $m=6;  #adapter minimum mapped nt
+if (defined $opts{'M'}) {$m=$opts{'M'};}
+
+my $t=1; #threads number
+if (defined $opts{'t'}) {$t=$opts{'t'};}
+
+my $min_nt=19; # minimum reads length
+if (defined $opts{'min'}) {$min_nt=$opts{'min'};}
+
+my $max_nt=28; #maximum reads length
+if (defined $opts{'max'}) {$max_nt=$opts{'max'};}
+
+my $mis=0; #mismatch number for microRNA
+if (defined $opts{'mis'}) {$mis=$opts{'mis'};}
+
+my $mis_rfam=0;# mismatch number for rfam
+if (defined $opts{'v'}) {$mis_rfam=$opts{'v'};}
+
+my (@filein,@mark,@clean);
+#&read_config();
+@filein=@inputfiles;
+@mark=@inputtags;
+
+&checkfa($opts{gfa});
+
+
+##### clip adpter --> clean data  start
+my $preprocess=$dir."preProcess_clean/";
+mkdir $preprocess;
+my $can_use_threads = eval 'use threads; 1';
+if ($can_use_threads) {
+# Do processing using threads
+	print "Do processing using threads\n";
+	my @filein1=@filein; my @mark1=@mark;
+	while (@filein1>0) {
+		my @thrs; my @res;
+		for (my $i=0;$i<$t ;$i++) {
+			last if(@filein1==0);
+			my $in=shift @filein1;
+			my $out=shift @mark1;
+			push @clean,$preprocess.$out."_clips_adapter.fq";
+			$thrs[$i]=threads->create(\&clips,$in,$out);
+		}
+		for (my $i=0;$i<@thrs;$i++) {
+			$res[$i]=$thrs[$i]->join();
+		}
+	}
+} else {
+# Do not processing using threads
+	print "Do not processing using threads\n";
+	for (my $i=0;$i<@filein ;$i++) {
+		my $in=$filein[$i];
+		my $out=$mark[$i];
+		push @clean,$preprocess.$out."_clips_adapter.fq";
+		&clips($in,$out);
+	}
+}
+
+##### clip adpter --> clean data  end
+
+my $collapsed=$preprocess."collapse_reads.fa";
+my $data=$preprocess."collapse_reads_${min_nt}_${max_nt}.fa"; ## raw clean data
+&collapse(\@clean,$collapsed);   #collapse reads to tags
+
+&filterbylength();  # filter <$min_nt  && >$max_nt
+
+print "The final clean data file is $data, only contains reads which length is among $min_nt\~$max_nt\n\n";
+
+my $clean_data=$preprocess."clean_data.fa";
+system("ln -s $data $clean_data");
+
+$time=Time();
+print "$time: Genome alignment!\n\n";
+my $genome_map=$dir."genome_match";
+&genome($data);
+#my $genome_map=&search($dir,"genome_match_");
+my $mapfile=$genome_map."/genome_mapped.bwt";
+my $mapfa=$genome_map."/genome_mapped.fa";
+my $unmap=$genome_map."/genome_not_mapped.fa";
+
+chdir $dir;
+my $pathfile="$dir/path.txt";
+open PA,">$pathfile";
+print PA "$config\n";
+print PA "$preprocess\n";
+print PA "$genome_map\n";
+
+if (defined $opts{'rfam'}) {              #rfam mapping and analysis
+	$time=Time();
+	print "$time: RNA annotate!\n\n";
+	$time=~s/:/-/g;
+	$time=~s/ /-/g;
+	my $rfam_exp_dir=$dir."rfam_match";
+	&rfam();
+	#my $rfam_exp_dir=&search($dir,"rfam_match_");
+print PA "$rfam_exp_dir\n";
+
+	my $tag=join "\\;" ,@mark;
+	system("perl $scipt_path/count_rfam_express.pl -i $rfam_exp_dir/rfam_mapped.bwt -tag $tag -o rfam_non-miRNA_annotation.txt");
+}
+
+
+close PA;
+system("perl $scipt_path/html_preprocess.pl -i $pathfile -format $format -min $min_nt -max $max_nt -o $dir/preprocessResult.html");
+
+$time=Time();
+print "$time: Program end!!\n";
+
+############################## sub programs ###################################
+sub genome{
+	my ($file)=@_;
+	if(defined $opts{'idx'}){
+		system("perl $scipt_path/matching.pl -i $file -g $opts{gfa} -r 1000 -v $mis -p $t -o $dir -index $opts{idx}") ;
+#		print "\nmatching.pl -i $file -g $opts{gfa} -v $mis -p $t -r $hit -o $dir -index $opts{idx} -time $time\n";
+	}else{
+		system("perl $scipt_path/matching.pl -i $file -g $opts{gfa} -r 1000 -v $mis -p $t -o $dir") ;
+#		print "\nmatching.pl -i $file -g $opts{gfa} -v $mis -p $t -r $hit -o $dir -time $time\n";
+	}
+}
+sub rfam{
+	if (defined $opts{'idx2'}) {
+		system("perl $scipt_path/rfam.pl -i $mapfa -ref $opts{rfam} -v $mis_rfam -p $t -o $dir -index $opts{idx2} ");
+#		print "\nrfam.pl -i $data2 -ref $opts{rfam} -v $mis_rfam -p $t -o $dir -index $opts{idx2} -time $time\n";
+	}else{
+		system("perl $scipt_path/rfam.pl -i $mapfa -ref $opts{rfam} -v $mis_rfam -p $t -o $dir ");
+#		print "\nrfam.pl -i $data2 -ref $opts{rfam} -v $mis_rfam -p $t -o $dir -time $time\n";
+	}
+}
+sub filterbylength{
+	my $tmpmark=join ",", @mark;
+	system("perl $scipt_path/filterReadsByLength.pl -i $collapsed -o $data -min $min_nt -max $max_nt -mark $tmpmark");
+	system("perl $scipt_path/Length_Distibution.pl -i $preprocess/reads_length_distribution.txt  -o $preprocess/length.html");
+#	print "\nfilterReadsByLength.pl -i $collapsed -o $data -min $min_nt -max $max_nt -mark $tmpmark\n";
+
+}
+sub collapse{
+	my ($ins,$data)=@_;
+		my $str="";
+	for (my $i=0;$i<@{$ins};$i++) {
+		$str .="-i $$ins[$i] ";
+	}
+	system ("perl $scipt_path/collapseReads2Tags.pl $str -mark seq -o $data -format $format");
+#	print "\ncollapseReads2Tags.pl $str -mark seq -o $data -format $format\n";
+}
+
+sub clips{
+	my ($in,$out)=@_;
+	my $adapter=$preprocess.$out."_clips_adapter.fq";
+	if($format eq "fq" || $format eq "fastq"){
+		system("fastx_clipper -a $a -M $m -Q $phred_qv -i $in -o $adapter") ;
+#		print "\nfastx_clipper -a $a -M $m -Q $phred_qv -i $in -o $adapter\n";
+	}
+	if($format eq "fa" || $format eq "fasta"){
+		system("fastx_clipper -a $a -M $m -i $in -o $adapter") ;
+        #		print "\nfastx_clipper -a $a -M $m -i $in -o $adapter\n";
+	}
+	#my $clean=$preprocess.$out."_clean.fq";
+	#system("filterReadsByLength.pl -i $adapter -o $clean -min $min_nt -max $max_nt ");
+
+	return;
+}
+
+sub read_config{
+	open CON,"<$config";
+	while (my $aline=<CON>) {
+		chomp $aline;
+		my @tmp=split/\t/,$aline;
+		push @filein,$tmp[0];
+		push @mark,$tmp[1];
+		&check_rawdata($tmp[0]);
+	}
+	close CON;
+	if (@filein != @mark) {
+		#&printErr();
+		die "Maybe config file have some wrong!!!\n";
+	}
+}
+sub check_rawdata{
+	my ($fileforcheck)=@_;
+	if (!(-s $fileforcheck)) {
+		#&printErr();
+		die "Can not find $fileforcheck, or file is empty!!!\n";
+	}
+	if ($format eq "fasta" || $format eq "fa") {
+		&checkfa($fileforcheck);
+	}
+	if ($format eq "fastq" || $format eq "fq") {
+		&checkfq($fileforcheck);
+	}
+}
+sub checkfa{
+	my ($file_reads)=@_;
+	open N,"<$file_reads";
+	my $line=<N>;
+	chomp $line;
+    if($line !~ /^>\S+/){
+        #printErr();
+        die "The first line of file $file_reads does not start with '>identifier'
+Reads file $file_reads is not a valid fasta file\n\n";
+    }
+    if(<N> !~ /^[ACGTNacgtn]*$/){
+        #printErr();
+        die "File $file_reads contains not allowed characters in sequences
+Allowed characters are ACGTN
+Reads file $file_reads is not a fasta file\n\n";
+    }
+	close N;
+}
+sub checkfq{
+	my ($file_reads)=@_;
+
+	open N,"<$file_reads";
+	for (my $i=0;$i<10;$i++) {
+		my $a=<N>;
+		my $b=<N>;
+		my $c=<N>;
+		my $d=<N>;
+		chomp $a;
+		chomp $b;
+		chomp $c;
+		chomp $d;
+		if($a!~/^\@/){
+			#&printErr();
+			die "$file_reads is not a fastq file\n\n";
+		}
+		if($b!~ /^[ACGTNacgtn]*$/){
+			#&printErr();
+			die "File $file_reads contains not allowed characters in sequences
+Allowed characters are ACGTN
+Reads file $file_reads is not a fasta file\n\n";
+		}
+		if ($c!~/^\@/ && $c!~/^\+/) {
+			#&printErr();
+			die "$file_reads is not a fastq file\n\n";
+		}
+		if ((length $b) != (length $d)) {
+			#&printErr();
+			die "$file_reads is not a fastq file\n\n";
+		}
+		my @qv=split //,$d;
+		for (my $j=0;$j<@qv ;$j++) {
+			my $q=ord($qv[$j])-64;
+			if($q<0){$phred_qv=33;}
+		}
+	}
+	close N;
+}
+
+sub search{
+	my ($dir,$str)=@_;
+	opendir I,$dir;
+	my @ret;
+	while (my $file=readdir I) {
+		if ($file=~/$str/) {
+			push @ret, $file;
+		}
+	}
+	closedir I;
+	if (@ret != 1) {
+		#&printErr();
+
+		die "Can not find directory or file which name has string: $str !!!\n";
+	}
+	return $ret[0];
+}
+
+sub Time{
+        my $time=time();
+        my ($sec,$min,$hour,$day,$month,$year) = (localtime($time))[0,1,2,3,4,5,6];
+        $month++;
+        $year+=1900;
+        if (length($sec) == 1) {$sec = "0"."$sec";}
+        if (length($min) == 1) {$min = "0"."$min";}
+        if (length($hour) == 1) {$hour = "0"."$hour";}
+        if (length($day) == 1) {$day = "0"."$day";}
+        if (length($month) == 1) {$month = "0"."$month";}
+        #print "$year-$month-$day $hour:$min:$sec\n";
+        return("$year-$month-$day $hour:$min:$sec");
+}
+
+
+sub usage{
+print <<"USAGE";
+Version $version
+Usage:
+$0 -i -format -gfa -index -rfam -a -M -min -max -mis -v -t  -o  -path
+options:
+-i input files, # raw data file, can be multipe eg. -i xxx.fq -i xxx .fq ...
+-tag string # raw data file names, -tag xxx -tag xxx
+
+-format string,#specific input rawdata file format : fastq|fq|fasta|fa
+-phred  int # phred quality number, default is 64
+
+-path scirpt path
+
+-gfa string,  input file # genome fasta. sequence file
+-idx string, 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
+
+-rfam string,  input file# rfam database file, microRNAs must not be contained in this file## if not define, rfam small RNA will not be count.
+-idx2 string,  rfam 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
+
+-a string,  ADAPTER string. default is ATCTCGTATG.
+-M int,    require minimum adapter alignment length of N. If less than N nucleotides aligned with the adapter - don't clip it. 
+-min int,  reads min length,default is 19.
+-max int,  reads max length,default is 28.
+
+-mis [int]     number of allowed mismatches when mapping reads to genome, default 0
+-v <int>     report end-to-end hits w/ <=v mismatches; ignore qualities,default 0; used in rfam alignment
+
+-t int,    number of threads [1]
+
+-o output directory# absolute path
+-h help
+USAGE
+exit(1);
+}
+