哪个是使用Bio :: Graphics绘制两个不同轨迹(染色体,片段,支架...)的最佳选择?

时间:2015-04-13 23:20:32

标签: perl graphics imagemagick coordinate-systems bioperl

我正在使用BioPerl模块Bio::Graphics绘制一些基因组坐标。我有来自不同支架或轨道的具有进化保守元素的区域,其想法是在相同的图中绘制相应的片段及其元素。我怎样才能做到这一点?

这是我的原始数据:

reftig_235  SNORD100    86265   86176   36171   136261  37251   37449   -   protein_coding.exon .   240680
reftig_235  SNORD100    86265   86176   36171   136261  52121   51889   -   RNAzCandidate   217 240680
reftig_235  SNORD100    86265   86176   36171   136261  37251   37449   -   protein_coding.exon .   240680
reftig_235  SNORD100    86265   86176   36171   136261  73633   73397   -   RNAzCandidate   224 240680
reftig_235  SNORD100    86265   86176   36171   136261  37251   37449   -   protein_coding.exon .   240680
reftig_235  SNORD100    86265   86176   36171   136261  114129  114369  +   RNAzCandidate   232 240680
reftig_235  SNORD100    86265   86176   36171   136261  37251   37449   -   protein_coding.exon .   240680
reftig_235  SNORD100    86265   86176   36171   136261  118835  119071  +   RNAzCandidate   224 240680
reftig_235  SNORD100    86265   86176   36171   136261  37251   37449   -   protein_coding.exon .   240680
reftig_235  SNORD100    86265   86176   36171   136261  130220  130454  +   RNAzCandidate   221 240680
reftig_235  SNORD100    86265   86176   36171   136261  37251   37449   -   protein_coding.exon .   240680
reftig_235  SNORD100    86265   86176   36171   136261  129525  129758  +   RNAzCandidate   219 240680
reftig_235  SNORD100    86265   86176   36171   136261  37251   37449   -   protein_coding.exon .   240680
reftig_2    SNORD100    86265   86176   36171   136261  124395  124625  +   RNAzCandidate   213 240680
reftig_2    SNORD100    86265   86176   36171   136261  37251   37449   -   protein_coding.exon .   240680
reftig_2    SNORD100    86265   86176   36171   136261  124687  124923  +   RNAzCandidate   224 240680

片段名称为:reftig_235和reftig_2。所以当我传递我的代码时:

#!/usr/bin/perl

# This is code example 3 in the Graphics-HOWTO
use strict;
use lib '/home/lstein/projects/bioperl-live';
use Bio::Graphics;
use Bio::SeqFeature::Generic;
use Data::Dumper;

my (@fill, @comparison, @db, @temp);
open my $IN, "< $ARGV[0]";

while (<$IN>){
    chomp $_;
    push @db, $_;
}

@temp = split /\t/, $db[0];
my $chrLen = $temp[11];
my $chrS = $temp[4];
my $chrE = $temp[5];
my $chr = $temp[0];
my $ann = $temp[9];
my $typ = $temp[1];

my $panel = Bio::Graphics::Panel->new(
  -length    => $chrLen, #longitud scala
  -width => 1500, #Ancho del gráfico
  -grid => 1,
  -pad_left  => 20,
  -pad_right => 20,
  -truetype => 1
  );

my $full_length = Bio::SeqFeature::Generic->new(
  -start => 0,
  -end   => $chrLen,
  -display_name => $chr,
                        );
my $partial_length = Bio::SeqFeature::Generic->new(
  -start => $chrS,
  -end   => $chrE,
  -display_name => "$chrS\-$chrE",
  );

$panel->add_track($full_length,
                  -key => $chr,
                  -glyph   => 'extending_arrow',
                  -tick    => 3,
                  -fgcolor => 'black',
                  -double  => 1,
                 );

$panel->add_track($partial_length,
                  -key => "$chrS\-$chrE",
                  -glyph   => 'extending_arrow',
                  -tick    => 3,
                  -fgcolor => 'blue',
                  -double  => 1,
                 );

my $track1 = $panel->add_track(
                #-category => 'HMMs'
                -key => 'ncRNAs by HMMs',
                -glyph => 'generic',
                #-glyph       => 'graded_segments',
                -label       => 1,
                -bgcolor     => 'lime',
                -stranded   => 1,
                              #-min_score   => 0,
                              #-max_score   => 240,
                -font2color  => 'black',
                -sort_order => 'left|longest',
                              #-sort_order  => 'high_score',
                              -description => sub {
                                my $feature = shift;
                                my $score   = $feature->score;
                                return "$typ";
                               },
                -bump => 3,
                #d-decorate_introns => 1,
                             );

my $track2 = $panel->add_track(
                #-category => 'Others',
                -key => 'RNAz Predictions',
                              #-glyph       => 'graded_segments',
                 -hbumppad => 1,
                -glyph       => 'transcript',
                #-height       => 7,
                -label       => 1,
                -bgcolor     => 'cyan',
                -min_score   => 0,
                -max_score   => 400,
                -strand_arrow   => 1,
                -label       => 1,
                -font2color  => 'red',
                -sort_order  => 'strand|left|longest',
                #-connector   => 'solid',
                -description => sub {
                                my $feature = shift;
                                my $score   = $feature->score;
                                return "RNAzAnn.; score=$score";
                               },
                             );


my $track3 = $panel->add_track( # Annotations
                -key => 'Genomic Annotations',
                -glyph       => 'transcript2',
                #-glyph       => 'transcript2',
                #-height      => 7,
                -label       => 1,
                -bgcolor     => 'teal',
                -min_score   => 0,
                -max_score   => 400,
                -strand_arrow   => 1,
                -label       => 1,
                -font2color  => 'purple',
                -sort_order  => 'strand|left|longest',
                -description => sub {
                                my $feature = shift;
                               #my $ann1   = $feature->annotation;
                                return "Ann.=$ann";
                               },
                             );


while (<>) { # read blast file
  chomp;
  next if /^\#/;  # ignore comments

#scaffold_401   5_8S_rRNA   3054    3211    0   22710   2620    2831    +   RNAzCandidate   176 22710
#scaffold_401   5_8S_rRNA   3054    3211    0   22710   13649   15877   -   Gaze.mRNA   .   22710
#reftig_235      SNORD100        86265   86176   36171   136261  86850   87250   +       RNAzCandidate   387    240680
#reftig_235      SNORD100        86265   86176   36171   136261  37251   37449   -       protein_coding.exon    .       240680

my($chr,$type,$startncRNA,$endncRNA,$startChr,$endChr, $startAnn, $endAnn, $sense, $annotation, $bitscore, $chrlen) = split /\t/;
    push @comparison, "$chr\.$type\.$startncRNA\.$endncRNA";
    my ($num,$sens, $sen, $se);
    #my $nameAnn = $annotation;
    #my @temp = (split /\;/, $nameAnn);
    #nameAnn =~ s/(^gene\_id\".*\")\;(.*)$/$1/g;
my ($feature1, $feature2, $feature3);
#if($startncRNA < $endncRNA){


if($startncRNA < $endncRNA){
    $sen = "+1";} else {
    $sen = "-1";}
    $feature1 = Bio::SeqFeature::Generic->new(
    -display_name => "\($startncRNA\-$endncRNA\)",
    -start        => $startncRNA,
    -end          => $endncRNA,
    -strand => $sen,
    );

if($annotation eq "RNAzCandidate"){
    if($startAnn < $endAnn){
    $sens = "+1";} else {
    $sens = "-1";}
    $feature2 = Bio::SeqFeature::Generic->new(
    -score        => $bitscore,
    -display_name => "\($startAnn\-$endAnn\)",
    -start        => $startAnn,
    -end          => $endAnn,
    -strand        => $sens,
    );
} elsif ($annotation ne "RNAzCandidate" && $bitscore eq "\."){
    if($sense eq "\+"){
    $se = "+1";} else { $se = "-1";}
    $feature3 = Bio::SeqFeature::Generic->new(
   -display_name => "\($startAnn\-$endAnn\)",
   -start        => $startAnn,
   -end          => $endAnn,
   -strand      => $se,
    );
} else {next;}
    $num = scalar @comparison;
    if ($num == 1){
    $track1->add_feature($feature1); #Anchor ncRNA
    $track2->add_feature($feature2); #RNAzCandidates
    $track3->add_feature($feature3); #Annotations
} else {
    my @split1 = split /\./, $comparison[-2];
    my @split2 = split /\./, $comparison[-1];
    if($split1[0] eq $split2[0] && $split1[1] eq $split2[1] && $split1[2] eq $split2[2] && $split1[3] eq $split2[3]){
        $track2->add_feature($feature2); #RNAzCandidates
        #$track3->add_feature($feature3); #Annotations
        shift @comparison;
        next;
    } else {
    $track1->add_feature($feature1); #Anchor ncRNA
    $track2->add_feature($feature2); #RNAzCandidates
    $track3->add_feature($feature3); #Annotations
    shift @comparison;
}}}
print $panel->gd->gif;

$panel->finished;
#print $panel->gif;

结果如下:

Plot generated by BioPerl, represent generic coordinates

但它没有绘制名为reftig_2的第二个片段。我能做什么? 提前谢谢!

0 个答案:

没有答案