| Bio-Graphics documentation | Contained in the Bio-Graphics distribution. |
Bio::Graphics::Glyph::ideogram - The "ideogram" glyph
See L<Bio::Graphics::Panel> and L<Bio::Graphics::Glyph>.
This glyph draws a section of a chromosome ideogram. It relies on certain data from the feature to determine which color should be used (stain) and whether the segment is a telomere or centromere or a regular cytoband. The centromeres and 'var'-marked bands are rendered with diagonal black-on-white patterns if the "-patterns" option is true, otherwise they are rendered in dark gray. This is to prevent a libgd2 crash on certain 64-bit platforms when rendering patterned images.
The cytobandband features would typically be formatted like this in GFF3:
...
ChrX UCSC cytoband 136700001 139000000 . . . Parent=ChrX;Name=Xq27.1;Alias=ChrXq27.1;stain=gpos75;
ChrX UCSC cytoband 139000001 140700000 . . . Parent=ChrX;Name=Xq27.2;Alias=ChrXq27.2;stain=gneg;
ChrX UCSC cytoband 140700001 145800000 . . . Parent=ChrX;Name=Xq27.3;Alias=ChrXq27.3;stain=gpos100;
ChrX UCSC cytoband 145800001 153692391 . . . Parent=ChrX;Name=Xq28;Alias=ChrXq28;stain=gneg;
ChrY UCSC cytoband 1 1300000 . . . Parent=ChrY;Name=Yp11.32;Alias=ChrYp11.32;stain=gneg;
which in this case is a GFF-ized cytoband coordinate file from UCSC:
http://hgdownload.cse.ucsc.edu/goldenPath/hg16/database/cytoBand.txt.gz
and the corresponding GBrowse config options would be like this to
create an ideogram overview track for the whole chromosome:
The 'chromosome' feature below would aggregated from bands and centromere using the default
chromosome aggregator
[CYT:overview]
feature = chromosome
glyph = ideogram
fgcolor = black
bgcolor = gneg:white gpos25:silver gpos50:gray
gpos:gray gpos75:darkgray gpos100:black acen:cen gvar:var
arcradius = 6
height = 25
bump = 0
label = 0
A script to reformat UCSC annotations to GFF3 format can be found at
the end of this documentation.
The following options are standard among all Glyphs. See Bio::Graphics::Glyph for a full explanation.
Option Description Default
------ ----------- -------
-fgcolor Foreground color black
-outlinecolor Synonym for -fgcolor
-linewidth Line width 1
-height Height of glyph 10
-font Glyph font gdSmallFont
-connector Connector type 0 (false)
-connector_color
Connector color black
-label Whether to draw a label 0 (false)
-description Whether to draw a description 0 (false)
The following options are specific to the ideogram glyph.
Option Description Default
------ ----------- -------
-bgcolor Band coloring string none
-bgfallback Coloring to use when no bands yellow
are present
-bgcolor is used to map each chromosome band's "stain" attribute into a color or pattern. It is a string that looks like this:
gneg:white gpos25:silver gpos50:gray \ gpos:gray gpos75:darkgray gpos100:black acen:cen gvar:var
This is saying to use "white" for features whose stain attribute is "gneg", "silver" for those whose stain attribute is "gpos25", and so on. Several special values are recognized: "stalk" draws a narrower gray region and is usually used to indicate an acrocentric stalk. "var" creates a diagonal black-on-white pattern. "cen" draws a centromere.
If -bgcolor is just a color name, like "yellow", the glyph will ignore all bands and just draw a filled in chromosome.
If -bgfallback is set to a color name or value, then the glyph will fall back to the indicated background color if the chromosome contains no bands.
The following short script can be used to convert a UCSC cytoband annotation file into GFF format. If you have the lynx web-browser installed you can call it like this in order to download and convert the data in a single operation:
fetchideogram.pl http://hgdownload.cse.ucsc.edu/goldenPath/hg18/database/cytoBand.txt.gz
Otherwise you will need to download the file first. Note the difference between this script and input data from previous versions of ideogram.pm: UCSC annotations are used in place of NCBI annotations.
#!/usr/bin/perl
use strict; my %stains; my %centros; my %chrom_ends;
foreach (@ARGV) { if (/^(ftp|http|https):/) { $_ = "lynx --dump $_ |gunzip -c|"; } elsif (/\.gz$/) { $_ = "gunzip -c $_ |"; } print STDERR "Processing $_\n"; }
print "##gff-version 3\n"; while(<>) { chomp; my($chr,$start,$stop,$band,$stain) = split /\t/; $start++; $chr = ucfirst($chr); if(!(exists($chrom_ends{$chr})) || $chrom_ends{$chr} < $stop) { $chrom_ends{$chr} = $stop; } my ($arm) = $band =~ /(p|q)\d+/; $stains{$stain} = 1; if ($stain eq 'acen') { $centros{$chr}->{$arm}->{start} = $stop; $centros{$chr}->{$arm}->{stop} = $start; next; } $chr =~ s/chr//i; print qq/$chr\tUCSC\tcytoband\t$start\t$stop\t.\t.\t.\tParent=$chr;Name=$chr;Alias=$chr$band;stain=$stain;\n/; }
foreach my $chr(sort keys %chrom_ends) { my $chr_orig = $chr; $chr =~ s/chr//i; print qq/$chr\tUCSC\tcentromere\t$centros{$chr_orig}->{p}->{stop}\t$centros{$chr_orig}->{q}->{start}\t.\t+\t.\tParent=$chr;Name=$chr\_cent\n/; }
Please report them.
Bio::Graphics::Panel, Bio::Graphics::Glyph, Bio::Graphics::Glyph::arrow, Bio::Graphics::Glyph::cds, Bio::Graphics::Glyph::crossbox, Bio::Graphics::Glyph::diamond, Bio::Graphics::Glyph::dna, Bio::Graphics::Glyph::dot, Bio::Graphics::Glyph::ellipse, Bio::Graphics::Glyph::extending_arrow, Bio::Graphics::Glyph::generic, Bio::Graphics::Glyph::graded_segments, Bio::Graphics::Glyph::heterogeneous_segments, Bio::Graphics::Glyph::line, Bio::Graphics::Glyph::pinsertion, Bio::Graphics::Glyph::primers, Bio::Graphics::Glyph::rndrect, Bio::Graphics::Glyph::segments, Bio::Graphics::Glyph::ruler_arrow, Bio::Graphics::Glyph::toomany, Bio::Graphics::Glyph::transcript, Bio::Graphics::Glyph::transcript2, Bio::Graphics::Glyph::translation, Bio::Graphics::Glyph::triangle, Bio::DB::GFF, Bio::SeqI, Bio::SeqFeatureI, Bio::Das, GD
Gudmundur A. Thorisson <mummi@cshl.edu>
Copyright (c) 2001-2006 Cold Spring Harbor Laboratory
Sheldon McKay <mckays@cshl.edu<gt>
This library is free software; you can redistribute it and/or modify it under the same terms as Perl itself. See DISCLAIMER.txt for disclaimers of warranty.
| Bio-Graphics documentation | Contained in the Bio-Graphics distribution. |
package Bio::Graphics::Glyph::ideogram; # $Id: ideogram.pm,v 1.11 2009-06-23 13:51:38 lstein Exp $ # Glyph to draw chromosome ideograms use strict qw/vars refs/; use vars '@ISA'; use GD; use base qw(Bio::Graphics::Glyph::generic Bio::Graphics::Glyph::heat_map); sub my_description { return <<END; This glyph draws a section of a chromosome ideogram. It relies on certain data from the feature to determine which color should be used (stain) and whether the segment is a telomere or centromere or a regular cytoband. See the full manual page for this glyph for instructions on formatting the ideogram. END } sub my_options { { bgcolor => [ 'string', ' gneg:white gpos25:silver gpos50:gray gpos:gray gpos75:darkgray gpos100:black acen:cen gvar:var', 'This option is redefined to map each chromosome band\'s "stain" attribute', 'into a color or pattern. The default value is saying to use ', '"white" for features whose stain attribute is', '"gneg", "silver" for those whose stain attribute is "gpos25", and so', 'on. Several special values are recognized: "B<stalk>" draws a narrower', 'gray region and is usually used to indicate an acrocentric', 'stalk. "B<var>" creates a diagonal black-on-white pattern if B<-pattern> is enabled.', '"B<cen>" draws a centromere.', 'If -bgcolor is just a color name, like "yellow", the glyph will ignore', 'all bands and just draw a filled in chromosome.'], bgfallback => [ 'color', 'yellow', 'Color to use when no bands are present.'], pattern => [ 'boolean', undef, 'Enable drawing a vertical line pattern for centromeres and "var" regions.', 'This is off by default due to an intermittent gd2 library crash on certain 64-bit platforms.'], } } sub demo_feature { my $self = shift; my $data = <<END; ##gff-version 3 22 ensembl chromosome 1 500 . . . ID=22;Name=Chr22 22 ensembl chromosome_band 1 30 . . . Parent=22;Name=p13;Alias=22p13;Stain=gvar 22 ensembl chromosome_band 31 66 . . . Parent=22;Name=p12;Alias=22p12;Stain=stalk 22 ensembl chromosome_band 67 97 . . . Parent=22;Name=p11.2;Alias=22p11.2;Stain=gvar 22 ensembl centromere 98 164 . . . Parent=22;Name=22_cent;Alias=2222_cent 22 ensembl chromosome_band 165 206 . . . Parent=22;Name=q11.21;Alias=22q11.21;Stain=gneg 22 ensembl chromosome_band 207 220 . . . Parent=22;Name=q11.22;Alias=22q11.22;Stain=gpos25 22 ensembl chromosome_band 221 245 . . . Parent=22;Name=q11.23;Alias=22q11.23;Stain=gneg 22 ensembl chromosome_band 246 281 . . . Parent=22;Name=q12.1;Alias=22q12.1;Stain=gpos50 22 ensembl chromosome_band 282 307 . . . Parent=22;Name=q12.2;Alias=22q12.2;Stain=gneg 22 ensembl chromosome_band 308 361 . . . Parent=22;Name=q12.3;Alias=22q12.3;Stain=gpos50 22 ensembl chromosome_band 362 396 . . . Parent=22;Name=q13.1;Alias=22q13.1;Stain=gneg 22 ensembl chromosome_band 397 430 . . . Parent=22;Name=q13.2;Alias=22q13.2;Stain=gpos50 22 ensembl chromosome_band 431 472 . . . Parent=22;Name=q13.31;Alias=22q13.31;Stain=gneg 22 ensembl chromosome_band 473 482 . . . Parent=22;Name=q13.32;Alias=22q13.32;Stain=gpos50 22 ensembl chromosome_band 483 500 . . . Parent=22;Name=q13.33;Alias=22q13.33;Stain=gneg END ; eval "require Bio::Graphics::FeatureFile" unless Bio::Graphics::FeatureFile->can('new'); my $db = Bio::Graphics::FeatureFile->new(-text=>$data) or die; return $db->get_features_by_name('Chr22'); } sub bgfallback { my $self = shift; return $self->option('bgfallback') || 'yellow'; } sub bgcolor { my $self = shift; my $bgcolor = $self->option('bgcolor'); return $bgcolor if defined $bgcolor; return 'gneg:white gpos25:silver gpos50:gray gpos:gray gpos75:darkgray gpos100:black acen:cen gvar:var'; } sub can_pattern { my $self = shift; return unless $self->option('pattern'); return $self->panel->image_class !~ /svg/i; } sub draw { my $self = shift; my ($gd,$left,$top,$partno,$total_parts) = @_; my $fstart = $self->feature->start; my $fstop = $self->feature->end; my @parts = $self->parts; # Draw the sides for the whole chromosome (in case # there are missing data). $self->draw_component(@_) if $self->level == 0; if (@parts) { $left += $self->left + $self->pad_left; $top += $self->top + $self->pad_top; } else { @parts = ($self); } # Make unaggregated bands invisible if requested. # This is for making image maps for individual # bands of whole aggregate chromosomes. $self->{invisible} ||= $self->option('invisible') unless @parts > 1; $parts[0]->{single}++ if @parts == 1; # if the bands are subfeatures of an aggregate chromosome, # we can draw the centomere and telomeres last to improve # the appearance my @last; for my $part (@parts) { push @last, $part and next if $part->feature->primary_tag =~ /centromere/i || $part->feature->start <= $fstart || $part->feature->end >= $fstop; my $tile = $part->create_tile('left'); $part->draw_component($gd,$left,$top); } for my $part (@last) { my $tile; if ($part->feature->method =~ /centromere/) { $tile = $self->create_tile('right'); } else { $tile = $part->create_tile('left'); } my $status = $part->{single} ? 'single' : $part->feature->method =~ /centromere/ ? 'centromere' : $part->feature->start <= $fstart ? 'left telomere' : $part->feature->end >= $fstop ? 'right telomere' : undef; $part->draw_component($gd,$left,$top,$status); } $self->draw_label(@_) if $self->option('label'); $self->draw_description(@_) if $self->option('description'); } sub draw_component { my $self = shift; my $gd = shift; my ($x,$y,$status) = @_; my $feat = $self->feature; my $arcradius = $self->option('arcradius') || 7; my ($x1, $y1, $x2, $y2 ) = $self->bounds(@_); return if $x2 <= $self->panel->left; return if $x1 >= $self->panel->right; $x2 = $self->panel->right if $x2 > $self->panel->right; # force odd width so telomere arcs are centered $y2 ++ if ($y2 - $y1) % 2; my ($stain) = $feat->get_tag_values('stain'); ($stain) = $feat->get_tag_values('Stain') unless $stain; # Some genome sequences don't contain substantial telomere sequence (i.e. Arabidopsis) # We can suggest their presence at the tips of the chromosomes by setting fake_telomeres = 1 # in the configuration file, resulting in the tips of the chromosome being painted black. my $fake_telomeres = $self->option('fake_telomeres') || 0; my $bgcolor_index = $self->bgcolor; if ((my $fallback = $self->bgfallback) && !$stain) { $bgcolor_index = $fallback; } elsif ($bgcolor_index =~ /\w+:/) { ($bgcolor_index) = $self->bgcolor =~ /$stain:(\S+)/ if $stain; ($bgcolor_index,$stain) = qw/white none/ if !$stain; } my $black = $gd->colorAllocate( 0, 0, 0 ); my $cm_color = $self->{cm_color} ||= $self->cm_color; my $var_color = $self->{var_color} ||= $self->var_color; my $bgcolor = $self->factory->translate_color($bgcolor_index); my $fgcolor = $self->fgcolor; # special color for gvar bands if ( $bgcolor_index =~ /var/) { $bgcolor = $self->can_pattern ? gdTiled : $var_color; } if ( $feat->method !~ /centromere/i && $stain ne 'acen') { # are we at the end of the chromosome? if (($status eq 'single' || $status eq 'left telomere') && $stain ne 'tip') { # left telomere my $state = $status eq 'single' ? -1 : $self->panel->flip ? 0 : 1; $bgcolor = $black if $fake_telomeres; $self->draw_telomere( $gd, $x1, $y1, $x2, $y2, $bgcolor, $fgcolor, $arcradius, $state ); } elsif ($status eq 'right telomere' && $stain ne 'tip') { # right telomere my $state = $self->panel->flip ? 1 : 0; $bgcolor = $black if $fake_telomeres; $self->draw_telomere( $gd, $x1, $y1, $x2, $y2, $bgcolor, $fgcolor, $arcradius, $state ); } # or a stalk? elsif ( $stain eq 'stalk') { $self->draw_stalk( $gd, $x1, $y1, $x2, $y2, $bgcolor, $fgcolor ); } # or a regular band? else { $self->draw_cytoband( $gd, $x1, $y1, $x2, $y2, $bgcolor, $fgcolor ); $self->draw_outline( $gd,$x1,$y1,$x2,$y2,$bgcolor,$fgcolor) if $bgcolor_index =~ /var/i; } } # or a centromere? else { if ( $self->can_pattern ) { my $tile = $self->create_tile('right'); $self->draw_centromere( $gd, $x1, $y1, $x2, $y2, gdTiled, $fgcolor ); } else { $self->draw_centromere( $gd, $x1, $y1, $x2, $y2, $cm_color, $fgcolor ); } } } sub draw_cytoband { my $self = shift; my ( $gd, $x1, $y1, $x2, $y2, $bgcolor, $fgcolor) = @_; # draw the filled box $self->filled_box($gd,$x1,$y1,$x2,$y2,$bgcolor,$bgcolor); # outer border $gd->line($x1,$y1,$x2,$y1,$fgcolor); $gd->line($x1,$y2,$x2,$y2,$fgcolor); } sub draw_outline { my $self = shift; my ( $gd, $x1, $y1, $x2, $y2, $bgcolor, $fgcolor) = @_; # side borders $gd->line($x1,$y1,$x1,$y2,$fgcolor); $gd->line($x2,$y1,$x2,$y2,$fgcolor); } sub draw_centromere { my $self = shift; my ( $gd, $x1, $y1, $x2, $y2, $bgcolor, $fgcolor ) = @_; # blank slate $self->wipe(@_); # draw a sort of hour-glass shape to represent the centromere my $poly = GD::Polygon->new; $poly->addPt( $x1, $y1 ); $poly->addPt( $x1, $y2 ); $poly->addPt( $x2, $y1 ); $poly->addPt( $x2, $y2 ); $gd->filledPolygon( $poly, $bgcolor ); # filled $gd->line( $x2 - 1, $y1 + 1, $x2 - 1, $y2 - 1, $fgcolor ); $gd->polygon( $poly, $fgcolor ); # outline } sub draw_telomere { my $self = shift; my ($gd, $x1, $y1, $x2, $y2, $bgcolor, $fgcolor, $arcradius, $state ) = @_; # blank slate $self->wipe(@_); # For single, unaggregated bands, make the terminal band # a bit wider to accomodate the arc if ($self->{single}) { $x1 -= 5 if $state == 1; $x2 += 5 if $state == 0; } # state should be one of: # 0 right telomere # 1 left telomere # -1 round at both ends (whole chromosome) my $outline++ if $state == -1; my $arcsize = $y2 - $y1; my $bwidth = $x2 - $x1; my $new_x1 = $x1 + $arcradius - 1; my $new_x2 = $x2 - $arcradius; my $new_y = $y1 + int($arcsize/2 + 0.5); my $orange = $self->panel->translate_color('lemonchiffon'); my $bg = $self->panel->bgcolor; $self->draw_cytoband( $gd, $x1, $y1, $x2, $y2, $bgcolor, $fgcolor ); $self->draw_outline( $gd, $x1, $y1, $x2, $y2, $bgcolor, $fgcolor ); if ( $state ) { # left telomere my $x = $new_x1; my $y = $new_y; # erase extra stuff $gd->line($x1,$y1,$x1+5,$y1,$bg); $gd->line($x1,$y1,$x1,$y2,$bg); $gd->line($x1,$y2,$x1+5,$y2,$bg); $gd->arc( $x, $y, $arcradius * 2, $arcsize, 90, 270, $fgcolor); # erase off-target colors $gd->fill($x1+1,$y1+1,$bg); $gd->fill($x1+1,$y2-1,$bg); } if ( $state < 1 ) { # right telomere my $x = $new_x2; my $y = $new_y; # erase extra stuff $gd->line($x2-5,$y1,$x2,$y1,$bg); $gd->line($x2,$y1,$x2,$y2,$bg); $gd->line($x2-5,$y2,$x2,$y2,$bg); $gd->arc( $x, $y, $arcradius * 2, $arcsize, 270, 90, $fgcolor); # erase off-target colors $gd->fill($x2-1,$y1+1,$bg); $gd->fill($x2-1,$y2-1,$bg); } unless ( $self->can_pattern ) { $self->draw_cytoband( $gd, $new_x1 - 1, $y1 + 2, $new_x1 + 1, $y2 - 2, $bgcolor, $bgcolor ); } } # for acrocentric stalk structure, draw a narrower cytoband sub draw_stalk { my $self = shift; my ( $gd, $x1, $y1, $x2, $y2, $bgcolor, $fgcolor, $inset ) = @_; # blank slate $self->wipe(@_); my $height = $self->height; $inset ||= $height > 10 ? int( $height / 10 + 0.5 ) : 2; $_[2] += $inset; $_[4] -= $inset; $self->draw_cytoband(@_); $gd->line( $x1, $y1, $x1, $y2, $fgcolor ); $gd->line( $x2, $y1, $x2, $y2, $fgcolor ); } sub create_tile { my $self = shift; my $direction = shift; my $gd = $self->panel->gd; return unless $gd->can('setTile'); # Prepare tile to use for filling an area my $tile; if ( $direction eq 'right' ) { $tile = GD::Image->new(3,3); my $black = $tile->colorAllocate(0,0,0); my $white = $tile->colorAllocate(255,255,255); $tile->filledRectangle(0, 0, 3, 3, $white); $tile->line( 0, 0, 3, 3, $black); } elsif ( $direction eq 'left' ) { $tile = GD::Image->new(4,4); my $black = $tile->colorAllocate(0,0,0); my $white = $tile->colorAllocate(255,255,255); $tile->filledRectangle(0,0,4,4, $white); $tile->line( 4, 0, 0, 4, $black); } $gd->setTile($tile); return $tile; } # This overrides the Glyph::parts method until I # can figure out how the bands get mangled there sub parts { my $self = shift; my $f = $self->feature; my $level = $self->level + 1; my @subf = sort {$a->start <=> $b->start} $f->get_SeqFeatures; return $self->factory->make_glyph($level,@subf); } # erase anthing that might collide. This is for # clean telomeres, centromeres and stalks sub wipe { my $self = shift; my $whitewash = $self->panel->bgcolor; $self->filled_box(@_[0..4],$whitewash,$whitewash); } # Disable bumping entirely, since it messes up the ideogram sub bump { return 0; } sub cm_color { my $self = shift; my $bgcolor = $self->bgcolor; my ($c) = $bgcolor =~ /cen:(\S+)/; $c ||= 'lightgrey'; return $self->translate_color($c); } sub var_color { my $self = shift; my $bgcolor = $self->bgcolor; my ($c) = $bgcolor =~ /var:(\S+)/; $c ||= '#805080'; return $self->translate_color($c); } 1; __END__