# HG changeset patch
# User dcouvin
# Date 1630708616 0
# Node ID 82dce1eb90743f47d791d06aa1b00da16c4dcd41

Uploaded

diff -r 000000000000 -r 82dce1eb9074 nucleScore.pl
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/nucleScore.pl	Fri Sep 03 22:36:56 2021 +0000
@@ -0,0 +1,241 @@
+#!/usr/bin/perl
+
+use strict;
+use warnings;
+use Bio::SeqIO;
+#use Shannon::Entropy qw/entropy/;
+use File::Basename;
+#use Bio::Species;
+
+#use FindBin;
+#use lib "$FindBin::RealBin/../perl5";
+
+#my $input = $ARGV[0];
+#chercher comment faire une liste perl pour input 
+#my @liste = split(/,/, $input);
+#my $recap_total_seq = $ARGV[1];
+
+#my ($input, $recap_total_seq) = @ARGV;
+
+#my $start = time();
+
+#my $file = ""; #= $ARGV[0];
+#my $recap_total_seq = "nucleScore_result.xls";
+
+#open (RECAP,'>', $recap_total_seq) or die "could not open $!";
+  print "File\tA percent\tT percent\tC percent\tG percent\tGC percent\tAT/GC ratio\tNucleScore\tATG\tTGA\tTAG\tTAA\tGenome size (bp)\n";
+#close(RECAP);
+
+
+#FASTA files
+#if(@ARGV){
+
+  #for (my $i = 0; $i <= $#ARGV; $i++) {
+    #if ($ARGV[$i]=~/-output/i or $ARGV[$i]=~/-o/i) {
+    #		$recap_total_seq = $ARGV[$i+1];
+    #}
+  #}
+
+
+ #open (RECAP,'>>', $recap_total_seq) or die "could not open $!";
+
+#refaire le for pour la liste input  	
+for my $arg (@ARGV){
+#for my $arg (@liste){
+#    if ($arg =~ m/.fasta/ or $arg =~ m/.fna/ or $arg =~ m/.fa/){
+
+	#print "Traitement du fichier de sequence: $arg\n";
+	#print "Traitement du fichier de sequence: $arg\n";
+	#my $file = $arg;
+	my $file = $arg;
+
+
+	my $seqIO = Bio::SeqIO->new(-format=>'Fasta', -file=>$file);
+	my $globalSeq = "";		
+	while (my $seq = $seqIO->next_seq()) {
+		my $seqID = $seq->id;
+		my $seqNuc = $seq->seq;
+		$globalSeq .= $seqNuc; 
+		#push @arrayID, $seqID;
+		#$hSeq{$seqID} = $seqNuc;
+		#my @seqArray = split //, $seqNuc;
+	}
+	
+	my $gcpercent = gc_percent($globalSeq);
+	my ($ade, $thy, $gua, $cyt, $n, $length) = number_nuc_length_seq($file);	
+	my ($aPercent, $tPercent, $gPercent, $cPercent, $nPercent) = nucleotid_percent($ade, $thy, $gua, $cyt, $n, $length);
+
+	my $atgcRatio =	 atgc_ratio($ade, $thy, $gua, $cyt);
+		
+	my @percentList = ($aPercent, $tPercent, $gPercent, $cPercent, $nPercent);
+		
+	my $variance = shift_data_variance(@percentList);
+	my $nucleScore = nucle_score($variance, $gcpercent, $atgcRatio, $length);
+	#my $entropy = entropy($globalSeq);
+	
+	#print "The sequence length for $file is: $length\n";		
+	#print "A percent: $aPercent\n";
+	#print "T percent: $tPercent\n";
+	#print "G percent: $gPercent\n";
+	#print "C percent: $cPercent\n";
+	#print "N percent: $nPercent\n";
+
+	#print "GC percent: $gcpercent\n";
+
+	#print "AT/GC ratio: $atgcRatio\n";
+
+	#print "NucleScore: $nucleScore\n";
+
+	#print "Shannon Entropy: $entropy\n\n";
+	
+	#print "3 digits:\n";
+	my @trinucs=($globalSeq=~/(?=(.{3}))/g);
+	my %tri_count=();
+	$tri_count{$_}++ for @trinucs;
+	#print $_,":",$tri_count{$_},"\n" for sort keys(%tri_count);	
+	#print "\n2 digits:\n";
+	my @trinucs2=($globalSeq=~/(?=(.{2}))/g);
+	my %tri_count2=();
+	$tri_count2{$_}++ for @trinucs2;
+	#print $_,":",$tri_count2{$_},"\n" for sort keys(%tri_count2);	
+	
+	my $atg = $tri_count{'ATG'};
+	my $tga = $tri_count{'TGA'};
+  	my $tag = $tri_count{'TAG'};
+	my $taa = $tri_count{'TAA'};
+	
+	#print "--------------------------------------\n\n";
+
+	my $label = basename($file);
+			
+	
+	#Summary file
+	#print RECAP "$file\t$aPercent\t$tPercent\t$cPercent\t$gPercent\t$gcpercent\t$atgcRatio\t$nucleScore\t$entropy\t$aaa\t$aat\n";
+	print "$label\t$aPercent\t$tPercent\t$cPercent\t$gPercent\t$gcpercent\t$atgcRatio\t$nucleScore\t$atg\t$tga\t$tag\t$taa\t$length\n";
+	#}
+  }
+  #close (RECAP) or die "close file error : $!";
+#}
+
+#my $end = time();
+
+#my $total = $end - $start;
+
+#print "***** Total time (in seconds) is: $total *****\n";
+
+#------------------------------------------------------------------------------
+# number nucleotid and length
+sub number_nuc_length_seq {
+	my ($fastaFile) = @_;
+	my $ade = 0;
+	my $thy = 0;
+	my $gua = 0;
+	my $cyt = 0;
+	my $n = 0;
+	my $length = 0;
+	
+	open (FASTA, "<", $fastaFile) or die "Could not open $!";
+	while (<FASTA>) {
+		chomp;
+		if ($_ !~ />/) {
+			my @seq = split //, $_;
+			
+			for my $nuc (@seq) {
+				$length +=1 ;
+				if ($nuc =~ /a/i) {$ade+=1;}
+				elsif ($nuc =~ /t/i) {$thy+=1;}
+				elsif ($nuc =~ /g/i) {$gua+=1;}
+				elsif ($nuc =~ /c/i) {$cyt+=1;}
+				elsif ($nuc =~ /n/i) {$n+=1;}
+			}
+		}
+	}
+	close(FASTA) or die "Error close file :$!";
+	return ($ade, $thy, $gua, $cyt, $n, $length);
+	
+}
+
+#------------------------------------------------------------------------------
+# compute percentage of nucleotid
+sub nucleotid_percent {
+	my($ade, $thy, $gua, $cyt, $n, $length) = @_;
+	
+	my $adePercent = $ade / $length * 100;
+	my $thyPercent = $thy / $length * 100;
+	my $guaPercent = $gua / $length * 100;
+	my $cytPercent = $cyt / $length * 100;
+	my $nPercent = $n / $length * 100;
+	
+	return ($adePercent, $thyPercent, $guaPercent, $cytPercent, $nPercent);
+	
+}
+
+#------------------------------------------------------------------------------
+# compute GC pourcent
+sub gc_percent {
+	my ($seq) = @_;
+	
+	my @charSeq = split(//, uc($seq));
+	my %hashFlank = ();
+
+	foreach my $v (@charSeq) {
+		$hashFlank{$v} += 1;  
+	}
+  
+	if (! $hashFlank{'G'}) { $hashFlank{'G'} = 0;}
+	if (! $hashFlank{'C'}) { $hashFlank{'C'} = 0;}
+
+	if(length($seq) == 0) {
+		return 0;
+	}
+	else {
+		return (($hashFlank{'G'} + $hashFlank{'C'}) / (length($seq))) * 100;
+	}
+	
+}
+#------------------------------------------------------------------------------
+# compute ATGC ratio 
+sub atgc_ratio {
+	my ($ade, $thy, $gua, $cyt) = @_;
+	
+	return (($ade + $thy) / ($gua + $cyt));
+	
+}
+#------------------------------------------------------------------------------
+# variance
+sub shift_data_variance {
+	my (@data) = @_;
+	
+	if ($#data + 1 < 2) { return 0.0; }
+
+	my $K = $data[0];
+	my ($n, $Ex, $Ex2) = 0.0;
+	
+	for my $x (@data) {
+		$n = $n + 1;
+		$Ex += $x - $K;
+		$Ex2 += ($x - $K) * ($x - $K);
+	}
+	
+	my $variance = ($Ex2 - ($Ex * $Ex) / $n) / ($n); ## ($n - 1)
+	
+	return $variance;
+
+}
+#------------------------------------------------------------------------------
+# nucle score
+#sub nucle_score {
+#	my ($variance, $gcPercent, $atgcRatio, $length) = @_;
+#	
+#	return (($variance * $gcPercent * $atgcRatio) / $length);
+#}
+sub nucle_score {
+	my ($variance, $gcPercent, $atgcRatio, $length) = @_;
+	return log2(($variance * $gcPercent * $atgcRatio ** (3)) / sqrt($length));
+}
+
+#------------------------------------------------------------------------------
+sub log2 {
+  my $n = shift;
+  return (log($n) / log(2));
+}
diff -r 000000000000 -r 82dce1eb9074 nuclescore.sample
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/nuclescore.sample	Fri Sep 03 22:36:56 2021 +0000
@@ -0,0 +1,281 @@
+<tool id="nuclescoretool" name="nuclescore" version="0.1.0">
+  <description>nuclescore</description>
+
+ 
+<command detect_errors="aggressive"><![CDATA[ 
+
+#import re
+        ## Creates symlinks for each input file based on the Galaxy 'element_identifier'
+        ## Used so that a human-readable name appears in the output table (instead of 'dataset_xyz.dat')
+        #set $named_input_files = ''
+        #for $input_file in $input_files
+            ## Add single quotes around each input file identifier
+            #set $_input_file = "'{}'".format($input_file.element_identifier)
+            ln -s '${input_file}' ${_input_file} &&
+            #set $named_input_files = $named_input_files + ' ' + $_input_file
+        #end for
+
+	perl '$__tool_directory__/nucleScore.pl' $_input_file $output
+
+	
+       
+
+]]></command>
+ <!-- ./nuclescore.sh ${named_input_files} > "$output" -->
+
+<inputs>
+  <param format="fasta" name="input_files" type="data" label="Genome fasta file : " multiple="true" display="checkboxes"/>
+</inputs>
+
+ <outputs>
+    <data format="tabular" name="output" />
+ </outputs>
+
+<help>
+No documentation
+  </help>
+
+</tool>
+
+
+-------------------------------------------------------------------------------------------------------------------------------------------------------------------
+
+#!/usr/bin/perl
+
+use strict;
+use warnings;
+use Bio::SeqIO;
+use Shannon::Entropy qw/entropy/;
+use File::Basename;
+#use Bio::Species;
+
+#use FindBin;
+#use lib "$FindBin::RealBin/../perl5";
+
+my $input = $ARGV[0];
+#chercher comment faire une liste perl pour input 
+my @liste = split(/,/, $input);
+my $recap_total_seq = $ARGV[1];
+
+#my ($input, $recap_total_seq) = @ARGV;
+
+my $start = time();
+
+#my $file = ""; #= $ARGV[0];
+#my $recap_total_seq = "nucleScore_result.xls";
+
+open (RECAP,'>', $recap_total_seq) or die "could not open $!";
+  print RECAP "File\tA percent\tT percent\tC percent\tG percent\tGC percent\tAT/GC ratio\tNucleScore\tShannon Entropy\tAAA\tAAT\n";
+close(RECAP);
+
+
+#FASTA files
+#if(@ARGV){
+
+  #for (my $i = 0; $i <= $#ARGV; $i++) {
+    #if ($ARGV[$i]=~/-output/i or $ARGV[$i]=~/-o/i) {
+    #		$recap_total_seq = $ARGV[$i+1];
+    #}
+  #}
+
+
+ open (RECAP,'>>', $recap_total_seq) or die "could not open $!";
+
+#refaire le for pour la liste input  	
+#for my $arg (@ARGV){
+for my $arg (@liste){
+#    if ($arg =~ m/.fasta/ or $arg =~ m/.fna/ or $arg =~ m/.fa/){
+
+	#print "Traitement du fichier de sequence: $arg\n";
+	print "Traitement du fichier de sequence: $arg\n";
+	#my $file = $arg;
+	my $file = $arg;
+
+
+	my $seqIO = Bio::SeqIO->new(-format=>'Fasta', -file=>$file);
+	my $globalSeq = "";		
+	while (my $seq = $seqIO->next_seq()) {
+		my $seqID = $seq->id;
+		my $seqNuc = $seq->seq;
+		$globalSeq .= $seqNuc; 
+		#push @arrayID, $seqID;
+		#$hSeq{$seqID} = $seqNuc;
+		#my @seqArray = split //, $seqNuc;
+	}
+	
+	my $gcpercent = gc_percent($globalSeq);
+	my ($ade, $thy, $gua, $cyt, $n, $length) = number_nuc_length_seq($file);	
+	my ($aPercent, $tPercent, $gPercent, $cPercent, $nPercent) = nucleotid_percent($ade, $thy, $gua, $cyt, $n, $length);
+
+	my $atgcRatio =	 atgc_ratio($ade, $thy, $gua, $cyt);
+		
+	my @percentList = ($aPercent, $tPercent, $gPercent, $cPercent, $nPercent);
+		
+	my $variance = shift_data_variance(@percentList);
+	my $nucleScore = nucle_score($variance, $gcpercent, $atgcRatio, $length);
+	my $entropy = entropy($globalSeq);
+	
+	print "The sequence length for $file is: $length\n";		
+	print "A percent: $aPercent\n";
+	print "T percent: $tPercent\n";
+	print "G percent: $gPercent\n";
+	print "C percent: $cPercent\n";
+	print "N percent: $nPercent\n";
+
+	print "GC percent: $gcpercent\n";
+
+	print "AT/GC ratio: $atgcRatio\n";
+
+	print "NucleScore: $nucleScore\n";
+
+	print "Shannon Entropy: $entropy\n\n";
+	
+	print "3 digits:\n";
+	my @trinucs=($globalSeq=~/(?=(.{3}))/g);
+	my %tri_count=();
+	$tri_count{$_}++ for @trinucs;
+	print $_,":",$tri_count{$_},"\n" for sort keys(%tri_count);	
+	print "\n2 digits:\n";
+	my @trinucs2=($globalSeq=~/(?=(.{2}))/g);
+	my %tri_count2=();
+	$tri_count2{$_}++ for @trinucs2;
+	print $_,":",$tri_count2{$_},"\n" for sort keys(%tri_count2);	
+	
+	my $aaa = $tri_count{'AAA'};
+	my $aat = $tri_count{'AAT'};
+	
+	print "--------------------------------------\n\n";
+
+	my $label = basename($file);
+			
+	
+	#Summary file
+	#print RECAP "$file\t$aPercent\t$tPercent\t$cPercent\t$gPercent\t$gcpercent\t$atgcRatio\t$nucleScore\t$entropy\t$aaa\t$aat\n";
+	print RECAP "$label\t$aPercent\t$tPercent\t$cPercent\t$gPercent\t$gcpercent\t$atgcRatio\t$nucleScore\t$entropy\t$aaa\t$aat\n";
+	#}
+  }
+  close (RECAP) or die "close file error : $!";
+#}
+
+my $end = time();
+
+my $total = $end - $start;
+
+print "***** Total time (in seconds) is: $total *****\n";
+
+#------------------------------------------------------------------------------
+# number nucleotid and length
+sub number_nuc_length_seq {
+	my ($fastaFile) = @_;
+	my $ade = 0;
+	my $thy = 0;
+	my $gua = 0;
+	my $cyt = 0;
+	my $n = 0;
+	my $length = 0;
+	
+	open (FASTA, "<", $fastaFile) or die "Could not open $!";
+	while (<FASTA>) {
+		chomp;
+		if ($_ !~ />/) {
+			my @seq = split //, $_;
+			
+			for my $nuc (@seq) {
+				$length +=1 ;
+				if ($nuc =~ /a/i) {$ade+=1;}
+				elsif ($nuc =~ /t/i) {$thy+=1;}
+				elsif ($nuc =~ /g/i) {$gua+=1;}
+				elsif ($nuc =~ /c/i) {$cyt+=1;}
+				elsif ($nuc =~ /n/i) {$n+=1;}
+			}
+		}
+	}
+	close(FASTA) or die "Error close file :$!";
+	return ($ade, $thy, $gua, $cyt, $n, $length);
+	
+}
+
+#------------------------------------------------------------------------------
+# compute percentage of nucleotid
+sub nucleotid_percent {
+	my($ade, $thy, $gua, $cyt, $n, $length) = @_;
+	
+	my $adePercent = $ade / $length * 100;
+	my $thyPercent = $thy / $length * 100;
+	my $guaPercent = $gua / $length * 100;
+	my $cytPercent = $cyt / $length * 100;
+	my $nPercent = $n / $length * 100;
+	
+	return ($adePercent, $thyPercent, $guaPercent, $cytPercent, $nPercent);
+	
+}
+
+#------------------------------------------------------------------------------
+# compute GC pourcent
+sub gc_percent {
+	my ($seq) = @_;
+	
+	my @charSeq = split(//, uc($seq));
+	my %hashFlank = ();
+
+	foreach my $v (@charSeq) {
+		$hashFlank{$v} += 1;  
+	}
+  
+	if (! $hashFlank{'G'}) { $hashFlank{'G'} = 0;}
+	if (! $hashFlank{'C'}) { $hashFlank{'C'} = 0;}
+
+	if(length($seq) == 0) {
+		return 0;
+	}
+	else {
+		return (($hashFlank{'G'} + $hashFlank{'C'}) / (length($seq))) * 100;
+	}
+	
+}
+#------------------------------------------------------------------------------
+# compute ATGC ratio 
+sub atgc_ratio {
+	my ($ade, $thy, $gua, $cyt) = @_;
+	
+	return (($ade + $thy) / ($gua + $cyt));
+	
+}
+#------------------------------------------------------------------------------
+# variance
+sub shift_data_variance {
+	my (@data) = @_;
+	
+	if ($#data + 1 < 2) { return 0.0; }
+
+	my $K = $data[0];
+	my ($n, $Ex, $Ex2) = 0.0;
+	
+	for my $x (@data) {
+		$n = $n + 1;
+		$Ex += $x - $K;
+		$Ex2 += ($x - $K) * ($x - $K);
+	}
+	
+	my $variance = ($Ex2 - ($Ex * $Ex) / $n) / ($n); ## ($n - 1)
+	
+	return $variance;
+
+}
+#------------------------------------------------------------------------------
+# nucle score
+#sub nucle_score {
+#	my ($variance, $gcPercent, $atgcRatio, $length) = @_;
+#	
+#	return (($variance * $gcPercent * $atgcRatio) / $length);
+#}
+sub nucle_score {
+	my ($variance, $gcPercent, $atgcRatio, $length) = @_;
+	return log2(($variance * $gcPercent * $atgcRatio) / sqrt($length));
+}
+
+#------------------------------------------------------------------------------
+sub log2 {
+  my $n = shift;
+  return (log($n) / log(2));
+}
diff -r 000000000000 -r 82dce1eb9074 nuclescore.sh
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/nuclescore.sh	Fri Sep 03 22:36:56 2021 +0000
@@ -0,0 +1,13 @@
+#!/bin/bash
+
+input=$1
+output=$2
+
+
+directory=`dirname $0`
+
+perl $directory/nucleScore.pl $input_files $output   
+
+#perl $directory/nucleScore.pl `echo $input | tr ',' ' '`  $output
+
+
diff -r 000000000000 -r 82dce1eb9074 nuclescore.xml
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/nuclescore.xml	Fri Sep 03 22:36:56 2021 +0000
@@ -0,0 +1,47 @@
+<tool id="nuclescore" name="NucleScore tool" version="0.1.0">
+  <description>allows to get information for classification of genome assemblies</description>
+
+<requirements>
+  <requirement type="package" version="1.7.2">perl-bioperl</requirement>
+</requirements>
+ 
+<command detect_errors="aggressive"><![CDATA[ 
+
+#import re
+        ## Creates symlinks for each input file based on the Galaxy 'element_identifier'
+        ## Used so that a human-readable name appears in the output table (instead of 'dataset_xyz.dat')
+        #set $named_input_files = ''
+        #for $input_file in $input_files
+            ## Add single quotes around each input file identifier
+            #set $_input_file = "'{}'".format($input_file.element_identifier)
+            ln -s '${input_file}' ${_input_file} && 
+            #set $named_input_files = $named_input_files + ' ' + $_input_file
+        #end for
+
+	
+  	perl '$__tool_directory__/nucleScore.pl' $named_input_files > "$output"
+	
+       
+
+]]></command>
+ <!-- perl '$__tool_directory__/nucleScore.pl' $_input_file > "$output"  -->
+ <!-- ./nuclescore.sh ${named_input_files} > "$output" -->
+
+<inputs>
+  <param format="fasta" name="input_files" type="data" label="Genome fasta file : " multiple="true" display="checkboxes"/>
+</inputs>
+
+ <outputs>
+    <data format="tabular" name="output" />
+ </outputs>
+
+<help><![CDATA[
+nucleScore.pl is a Perl script allowing to get information for classification of genome assemblies basing on nucleotides data (GC percent, AT/GC ratio, ...)
+
+This script belongs to the getSequenceInfo supplementary tools
+
+- GitHub: https://github.com/karubiotools/getSequenceInfo/tree/master/supplementary_tools
+]]>
+</help>
+
+</tool>
diff -r 000000000000 -r 82dce1eb9074 output.xls
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/output.xls	Fri Sep 03 22:36:56 2021 +0000
@@ -0,0 +1,2 @@
+File	A percent	T percent	C percent	G percent	GC percent	AT/GC ratio	NucleScore	Shannon Entropy	AAA	AAT
+exemple_sequence_AFRI2a.fasta	17.2865811379154	17.2254003843317	32.9175761234243	32.5704423543286	65.4880184777529	0.526996881635245	1.30199532029328	1.92961990163878	22633	24339