/
merge-boundaries.pl
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merge-boundaries.pl
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#!/usr/bin/env perl
# merge-boundaries.pl
# Mike Covington
# created: 2013-08-07
#
# Description:
#
use strict;
use warnings;
use Log::Reproducible;
use autodie;
use feature 'say';
use Number::RangeTracker;
use List::Util qw(min max sum);
use Getopt::Long;
#TODO: Add usage statement
# Temporary defaults values:
my $chr_list = "A01,A02,A03,A04,A05,A06,A07,A08,A09,A10";
my $bam_file = "~/git.repos/sample-files/bam/IMB211.good.bam";
my $chr_termini;
my $options = GetOptions(
"chr_list=s" => \$chr_list,
"bam_file=s" => \$bam_file,
"chr_termini" => \$chr_termini,
);
my @boundary_files = @ARGV; # || qw(sample-file/RIL_300.boundaries sample-file/RIL_300.boundaries);
my @chromosomes = split /,/, $chr_list;
my $chr_lengths = get_chr_lengths( $bam_file, \@chromosomes );
my %range;
for my $chr (@chromosomes) {
$range{$chr} = Number::RangeTracker->new();
}
for my $file (@boundary_files) {
open my $boundary_fh, "<", $file;
my %boundaries;
while (<$boundary_fh>) {
my ( $chr, $start, $end ) = split;
$boundaries{$chr}{$start} = $end;
}
for my $chr (@chromosomes) {
my $end = 0;
for my $start ( sort { $a <=> $b } keys %{ $boundaries{$chr} } ) {
if ( $end == 0 && $chr_termini ) {
$range{$chr}->add( $start - 1, $start - 1 );
}
else {
$range{$chr}->add( $end + 1, $start - 1 );
}
$end = $boundaries{$chr}{$start};
}
if ($chr_termini) {
$range{$chr}->add( $end + 1, $end + 1 );
}
else {
$range{$chr}->add( $end + 1, $chr_lengths->{$chr} );
}
}
}
my %borders;
my %bins;
for my $chr (@chromosomes) {
%{ $borders{$chr} } = $range{$chr}->output;
%{ $bins{$chr} } = $range{$chr}->complement( 1, $chr_lengths->{$chr} );
}
# TODO: Write bin boundaries to file
say "BORDER SIZES:";
for my $chr (@chromosomes) {
my @lengths;
for my $start ( sort { $a <=> $b } keys %{ $borders{$chr} } ) {
push @lengths, $borders{$chr}->{$start} - $start + 1;
}
summarize_ranges( $chr, \@lengths ) if scalar @lengths;
}
say "BIN SIZES:";
open my $bin_fh, ">", "bins.tsv";
say $bin_fh join "\t", "chr", "start", "end";
for my $chr (@chromosomes) {
my @lengths;
for my $start ( sort { $a <=> $b } keys %{ $bins{$chr} } ) {
my $end = $bins{$chr}->{$start};
push @lengths, $end - $start + 1;
say $bin_fh join "\t", $chr, $start, $end;
}
summarize_ranges( $chr, \@lengths ) if scalar @lengths;
}
close $bin_fh;
exit;
sub get_chr_lengths {
my ( $bam_file, $chromosomes ) = @_;
my %chr_lengths = map { $_ => 0 } @{$chromosomes};
my $chr_count = scalar @{$chromosomes};
open my $bam_head_fh, "-|", "samtools view -H $bam_file";
while (<$bam_head_fh>) {
next unless /^\@SQ/;
my ( $seq_id, $seq_len ) = $_ =~ m/\tSN:([^\t]+)\tLN:(\d+)/;
next # only skip 'nonexistent' chromosomes if custom list is supplied
if $chr_count > 0
&& !exists $chr_lengths{$seq_id};
$chr_lengths{$seq_id} = $seq_len;
}
close $bam_head_fh;
return \%chr_lengths;
}
sub summarize_ranges {
my ( $chr, $lengths ) = @_;
my $count = scalar @$lengths;
my $min = min @$lengths;
my $median = median(@$lengths);
my $mean = mean(@$lengths);
my $max = max @$lengths;
my $summary = <<END_SUMMARY;
$chr
count: $count
min: $min
median: $median
mean: $mean
max: $max
END_SUMMARY
say $summary;
}
sub mean {
my @values = @_;
my $count = scalar @values;
return int sum(@values) / $count; # truncate decimals for these summaries
}
sub median {
my @unsorted_values = @_;
my @values = sort { $a <=> $b } @unsorted_values;
my $count = scalar @values;
my $mid = int @values / 2;
my $median;
if ( $count == 0 ) {
warn "WARNING: No values passed to median()";
}
elsif ( $count == 1 ) {
$median = $values[0];
}
elsif ( $count == 2 ) {
$median = mean(@values);
}
elsif ( @values % 2 ) {
$median = $values[$mid];
}
else {
$median = mean( $values[$mid], $values[ $mid + 1 ] );
}
return $median;
}