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nucleotide-freqs.pl
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#!/usr/bin/env perl
# ___UNDOCUMENTED___
use warnings;
use strict;
use Data::Dumper;
use Carp;
use Getopt::Long;
use Pod::Usage;
# Check required command line parameters
pod2usage ( -verbose => 1 )
unless @ARGV;
my $kmer = 2;
my @excluded_sequences;
my $alphabet = 'ACGT';
my $output;
# Grabs and parses command line options
my $result = GetOptions (
'kmer|k=i' => \$kmer,
'exclude-seq|x=s{,}' => \@excluded_sequences,
'alphabet|a=s' => \$alphabet,
'output|o=s' => \$output,
'verbose|v' => sub { use diagnostics; },
'quiet|q' => sub { no warnings; },
'help|h' => sub { pod2usage ( -verbose => 1 ); },
'manual|m' => sub { pod2usage ( -verbose => 2 ); }
);
if ($output) {
open my $USER_OUT, '>', $output or carp "Can't open $output for writing: $!";
select $USER_OUT;
}
my $reference = $ARGV[0];
my %reference = %{ index_fasta ($reference, join "|", @excluded_sequences) };
my %nucleotide_frequencies;
for my $k (1, $kmer) {
print STDERR "#k:\t$k\n";
my %frequencies = ();
my $total_length = 0;
for my $chromosome (sort keys %reference) {
next if $chromosome =~ m/-length/;
$total_length += $reference{"$chromosome-length"};
print STDERR "#chromosome:\t$chromosome\n";
print STDERR "#length:\t", $reference{"$chromosome-length"}, "\n";
my %frequency = %{ word_composition ($reference{$chromosome}, $k) };
for my $word (sort keys %frequency) {
next if $word =~ m/[^$alphabet]/i;
$frequencies{$word} += $frequency{$word};
print STDERR join ("\t",
$word,
$frequency{$word},
$frequency{$word} / $reference{"$chromosome-length"},
), "\n";
}
}
print STDERR "#all:\n";
print STDERR "#length:$total_length\n";
print join ("\t",
'#word',
'#count',
'#size',
'#observed',
'#expected',
'#obs/expect',
'#independent',
), "\n"
if $k > 1;
for my $word (sort keys %frequencies) {
next if $word =~ m/[^$alphabet]/i;
if ($k == 1) {
$nucleotide_frequencies{$word} = $frequencies{$word} / $total_length;
print STDERR join ("\t",
$word,
$nucleotide_frequencies{$word},
), "\n";
}
else {
my $observed = $frequencies{$word} / $total_length;
my $expected = 1;
map {$expected *= $nucleotide_frequencies{$_}} (split //, $word);
print join ("\t",
$word,
$frequencies{$word},
$total_length,
$observed,
$expected,
$observed / $expected,
map {$nucleotide_frequencies{$_} * $total_length} (split //, $word),
), "\n";
}
}
}
sub word_composition {
my ($sequence, $k, $alphabet) = @_;
my %frequency = ();
for (0 .. length ($sequence) - $k) {
my $word = substr $sequence, $_, $k;
next if $word =~ m/[^ACGT]/i;
$frequency{$word}++;
}
return \%frequency;
}
sub index_fasta {
my $reference_file = shift;
my $excluded_sequences = shift;
my %reference = ();
return \%reference unless $reference_file;
# reads in the reference genome file into @fastaseq
open my $REF, '<', "$reference_file"
or croak "Can't open $reference for reading: $!";
my @fastaseq = <$REF>;
close $REF;
# find and store indices for each chromosome change and corresponding descriptions
my ( @idx, @dsc ) = ();
for my $i ( 0 .. @fastaseq - 1 ) {
if ( $fastaseq[$i] =~ m/^>/ ) {
$fastaseq[$i] =~ s/>//g;
$fastaseq[$i] = ( split /\s/, "$fastaseq[$i]" )[0];
next if grep {m/$excluded_sequences/i} $fastaseq[$i];
push @idx, $i;
push @dsc, $fastaseq[$i];
}
}
for my $j ( 0 .. @idx - 1 ) {
my $line;
if ( $j == scalar @idx - 1 ) {
$line = join( q{}, @fastaseq[ $idx[$j] + 1 .. @fastaseq - 1]);
}
else {
$line = join( q{}, @fastaseq[ $idx[$j] + 1 .. $idx[$j + 1] - 1]);
}
$line =~ s/[\n\r]//g;
my $length = $line =~ tr/ACGT//;
$reference{$dsc[$j]} = $line;
$reference{"$dsc[$j]-length"} = $length;
}
return \%reference;
}
__END__
=head1 NAME
name.pl - Short description
=head1 SYNOPSIS
=head1 DESCRIPTION
=head1 OPTIONS
name.pl [OPTION]... [FILE]...
-o, --output filename to write results to (defaults to STDOUT)
-v, --verbose output perl's diagnostic and warning messages
-q, --quiet supress perl's diagnostic and warning messages
-h, --help print this information
-m, --manual print the plain old documentation page
=head1 REVISION
Version 0.0.1
$Rev: 249 $:
$Author: psilva $:
$Date: 2010-01-11 21:24:34 -0800 (Mon, 11 Jan 2010) $:
$HeadURL: http://dzlab.pmb.berkeley.edu/svn/bisulfite/trunk/nucleotide-freqs.pl $:
$Id: nucleotide-freqs.pl 249 2010-01-12 05:24:34Z psilva $:
=head1 AUTHOR
Pedro Silva <[email protected]/>
Zilberman Lab <http://dzlab.pmb.berkeley.edu/>
Plant and Microbial Biology Department
College of Natural Resources
University of California, Berkeley
=head1 COPYRIGHT
This program is free software: you can redistribute it and/or modify
it under the terms of the GNU General Public License as published by
the Free Software Foundation, either version 3 of the License, or
(at your option) any later version.
This program is distributed in the hope that it will be useful,
but WITHOUT ANY WARRANTY; without even the implied warranty of
MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the
GNU General Public License for more details.
You should have received a copy of the GNU General Public License
along with this program. If not, see <http://www.gnu.org/licenses/>.
=cut