#
# BioPerl module for Bio::SeqIO::tigrxml
#
# Please direct questions and support issues to <bioperl-l@bioperl.org>
#
# Cared for by Jason Stajich <jason-at-bioperl-dot-org>
#
# Copyright Jason Stajich
#
# You may distribute this module under the same terms as perl itself
# POD documentation - main docs before the code
=head1 NAME
Bio::SeqIO::tigrxml - Parse TIGR (new) XML
=head1 SYNOPSIS
use Bio::SeqIO;
my $in = Bio::SeqIO->new(-format => 'tigrcoordset',
-file => 'file.xml');
while( my $seq = $in->next_seq ) {
# do something...
}
=head1 DESCRIPTION
This is a parser for TIGR Coordset XML for their in-progress
annotation dbs.
=head1 FEEDBACK
=head2 Mailing Lists
User feedback is an integral part of the evolution of this and other
Bioperl modules. Send your comments and suggestions preferably to
the Bioperl mailing list. Your participation is much appreciated.
bioperl-l@bioperl.org - General discussion
http://bioperl.org/wiki/Mailing_lists - About the mailing lists
=head2 Support
Please direct usage questions or support issues to the mailing list:
I<bioperl-l@bioperl.org>
rather than to the module maintainer directly. Many experienced and
reponsive experts will be able look at the problem and quickly
address it. Please include a thorough description of the problem
with code and data examples if at all possible.
=head2 Reporting Bugs
Report bugs to the Bioperl bug tracking system to help us keep track
of the bugs and their resolution. Bug reports can be submitted via the
web:
https://redmine.open-bio.org/projects/bioperl/
=head1 AUTHOR - Jason Stajich
Email jason-at-bioperl-dot-org
=head1 APPENDIX
The rest of the documentation details each of the object methods.
Internal methods are usually preceded with a _
=cut
# Let the code begin...
package Bio::SeqIO::tigrxml;
use vars qw($Default_Source);
use strict;
use XML::SAX;
use XML::SAX::Writer;
use Data::Dumper;
use Bio::Seq::SeqFactory;
use Bio::Species;
use Bio::SeqFeature::Generic;
use Bio::Annotation::Reference;
use Bio::Annotation::Comment;
use Bio::Annotation::DBLink;
use List::Util qw(min max);
use base qw(Bio::SeqIO XML::SAX::Base);
$Default_Source = 'TIGR';
sub _initialize {
my ($self) = shift;
$self->SUPER::_initialize(@_);
$self->{'_parser'} = XML::SAX::ParserFactory->parser('Handler' => $self);
if( ! defined $self->sequence_factory ) {
$self->sequence_factory(Bio::Seq::SeqFactory->new
(-verbose => $self->verbose(),
-type => 'Bio::Seq::RichSeq'));
}
return;
}
sub next_seq {
my $self = shift;
if( @{$self->{'_seendata'}->{'_seqs'} || []} ||
eof($self->_fh)) {
return shift @{$self->{'_seendata'}->{'_seqs'}};
}
$self->{'_parser'}->parse_file($self->_fh);
return shift @{$self->{'_seendata'}->{'_seqs'}};
}
# XML::SAX::Base methods
sub start_document {
my ($self,$doc) = @_;
$self->{'_seendata'} = {'_seqs' => [],
'_authors' => [],
'_feats' => [] };
$self->SUPER::start_document($doc);
}
sub end_document {
my ($self,$doc) = @_;
$self->SUPER::end_document($doc);
}
sub start_element {
my ($self,$ele) = @_;
# attributes
my $name = uc $ele->{'LocalName'};
my $attr = $ele->{'Attributes'};
my $seqid = defined $self->{'_seendata'}->{'_seqs'}->[-1] ?
$self->{'_seendata'}->{'_seqs'}->[-1]->display_id : undef;
# we're going to try and be SO-nice here
if( $name eq 'ASSEMBLY' ) { # New sequence
my ($len) = $attr->{'{}COORDS'}->{'Value'} =~ /\d+\-(\d+)/;
push @{$self->{'_seendata'}->{'_seqs'}},
$self->sequence_factory->create
(
-display_id => $attr->{'{}ASMBL_ID'}->{'Value'},
-length => $len,
);
} elsif( $name eq 'HEADER' ) {
} elsif( $name eq 'CLONE_NAME' ) {
} elsif( $name eq 'ORGANISM' ) {
} elsif( $name eq 'AUTHOR_LIST' ) {
$self->{'_seendata'}->{'_authors'} = [];
} elsif( $name eq 'TU' ) { # gene feature
my ($s,$e) = ($attr->{'{}COORDS'}->{'Value'} =~ /(\d+)\-(\d+)/);
my $strand = 1;
if( $s > $e) {
($s,$e,$strand) = ( $e,$s,-1);
}
my $fname = $attr->{'{}FEAT_NAME'}->{'Value'};
my $f = Bio::SeqFeature::Generic->new
(-seq_id => $seqid,
-start => $s,
-end => $e,
-strand => $strand,
-primary_tag => 'gene', # what does this really map to?
-source_tag => $Default_Source,
-tag => {
'Note' => $attr->{'{}COM_NAME'}->{'Value'},
'ID' => $fname,
'locus' => $attr->{'{}LOCUS'}->{'Value'},
'pub_locus' => $attr->{'{}PUB_LOCUS'}->{'Value'},
'alt_locus' => $attr->{'{}ALT_LOCUS'}->{'Value'},
'pub_comment' => $attr->{'{}PUB_COMMENT'}->{'Value'},
}
);
push @{$self->{'_seendata'}->{'_feats'}}, $f;
# add this feature to the current sequence
$self->{'_seendata'}->{'_seqs'}->[-1]->add_SeqFeature($f);
} elsif( $name eq 'MODEL' ) { # mRNA/transcript
# reset the UTRs
$self->{'_seendata'}->{"five_prime_UTR"}= undef;
$self->{'_seendata'}->{"three_prime_UTR"} = undef;
my ($s,$e) = ($attr->{'{}COORDS'}->{'Value'} =~ /(\d+)\-(\d+)/);
my $strand = 1;
if( $s > $e) {
($s,$e,$strand) = ( $e,$s,-1);
}
my $parent = $self->{'_seendata'}->{'_feats'}->[-1];
my ($parentid) = $parent->get_tag_values('ID');
my $f = Bio::SeqFeature::Generic->new
(-primary_tag => 'transcript',
-source_tag => $Default_Source,
-start => $s, # we use parent start/stop because 'MODEL' means CDS start/stop
-end => $e, # but we want to reflect
-strand => $strand,
-seq_id => $seqid,
-tag => {
'ID' => $attr->{'{}FEAT_NAME'}->{'Value'},
'Parent' => $parentid,
'Note' => $attr->{'{}COMMENT'}->{'Value'},
});
$parent->add_SeqFeature($f);
push @{$self->{'_seendata'}->{'_feats'}}, $f;
$self->{'_seendata'}->{'_seqs'}->[-1]->add_SeqFeature($f);
} elsif( $name eq 'EXON' ) { # exon feature
my ($s,$e) = ($attr->{'{}COORDS'}->{'Value'} =~ /(\d+)\-(\d+)/);
my $strand = 1;
if( $s > $e) {
($s,$e,$strand) = ( $e,$s,-1);
}
my $parent = $self->{'_seendata'}->{'_feats'}->[-1];
my ($parentid) = $parent->get_tag_values('ID');
my $f = Bio::SeqFeature::Generic->new
(-primary_tag => 'exon',
-source_tag => $Default_Source,
-seq_id => $seqid,
-start => $s,
-end => $e,
-strand => $strand,
-tag => {
'ID' => $attr->{'{}FEAT_NAME'}->{'Value'},
'Parent' => $parentid,
});
$parent->add_SeqFeature($f,'EXPAND');
$self->{'_seendata'}->{'_seqs'}->[-1]->add_SeqFeature($f);
# we'll still just add exons to the transcript
} elsif( $name eq 'PROTEIN_SEQ' ) {
} elsif( $name eq 'CDS' ) {
# CDS will be the translation of the transcript
my ($s,$e) = ($attr->{'{}COORDS'}->{'Value'} =~ /(\d+)\-(\d+)/);
my $strand = 1;
if( $s > $e) {
($s,$e,$strand) = ( $e,$s,-1);
}
my $parent = $self->{'_seendata'}->{'_feats'}->[-1];
my ($parentid) = $parent->get_tag_values('ID');
$self->assert($parent->primary_tag eq 'transcript', 'Testing for primary tag equivalent to mRNA');
$self->assert($parent->strand == $strand || abs($s-$e) == 0, 'Testing that parent feature and current feature strand are equal '. $parentid. ' '.$attr->{'{}FEAT_NAME'}->{'Value'});
my $f = Bio::SeqFeature::Generic->new
(-primary_tag => 'CDS',
-source_tag => $Default_Source,
-seq_id => $seqid,
-start => $s,
-end => $e,
-strand => $parent->strand,
-tag => {
'ID' => $attr->{'{}FEAT_NAME'}->{'Value'},
'Parent' => $parentid, # should be the mRNA
});
$parent->add_SeqFeature($f);
$self->{'_seendata'}->{'_seqs'}->[-1]->add_SeqFeature($f);
} elsif( $name eq 'RNA-EXON' ) {
my ($s,$e) = ($attr->{'{}COORDS'}->{'Value'} =~ /(\d+)\-(\d+)/);
my $strand = 1;
if( $s > $e) {
($s,$e,$strand) = ( $e,$s,-1);
}
my $parent = $self->{'_seendata'}->{'_feats'}->[-1];
my ($parentid) = $parent->get_tag_values('ID');
my $f = Bio::SeqFeature::Generic->new
(-primary_tag => 'tRNA_exon', # tRNA_exon?
-source_tag => $Default_Source,
-seq_id => $seqid,
-start => $s,
-end => $e,
-strand => $strand,
-tag => {
'ID' => $attr->{'{}FEAT_NAME'}->{'Value'},
'Parent' => $parentid,
}
);
$parent->add_SeqFeature($f);
$self->{'_seendata'}->{'_seqs'}->[-1]->add_SeqFeature($f);
} elsif( $name eq 'PRE-TRNA' ) { # tRNA gene
my ($s,$e) = ( $attr->{'{}COORDS'}->{'Value'} =~/(\d+)\-(\d+)/);
my $strand = 1;
if( $s > $e) {
($s,$e,$strand) = ( $e,$s,-1);
}
my $f = Bio::SeqFeature::Generic->new
( -primary_tag => 'tRNA_coding_gene',
-source_tag => $Default_Source,
-seq_id => $seqid,
-start => $s,
-end => $e,
-strand => $strand,
-tag => {'ID' => $attr->{'{}FEAT_NAME'}->{'Value'},
}
);
push @{$self->{'_seendata'}->{'_feats'}}, $f;
$self->{'_seendata'}->{'_seqs'}->[-1]->add_SeqFeature($f);
} elsif( $name eq 'TRNA' ) { # tRNA transcript
my ($s,$e) = ($attr->{'{}COORDS'}->{'Value'} =~ /(\d+)\-(\d+)/);
my $strand = 1;
if( $s > $e) {
($s,$e,$strand) = ( $e,$s,-1);
}
my $parent = $self->{'_seendata'}->{'_feats'}->[-1];
my ($parentid) = $parent->get_tag_values('ID');
my $f = Bio::SeqFeature::Generic->new
(-primary_tag => 'tRNA_primary_transcript',
-source_tag => $Default_Source,
-start => $s,
-end => $e,
-strand => $strand,
-seq_id => $seqid,
-tag => {
'ID' => $attr->{'{}FEAT_NAME'}->{'Value'},
'Parent' => $parentid,
'Note' => $attr->{'{}COM_NAME'}->{'Value'},
'anticodon' => $attr->{'{}ANTICODON'}->{'Value'},
'pub_locus' => $attr->{'{}PUB_LOCUS'}->{'Value'},
});
$parent->add_SeqFeature($f);
push @{$self->{'_seendata'}->{'_feats'}}, $f;
$self->{'_seendata'}->{'_seqs'}->[-1]->add_SeqFeature($f);
} elsif( $name eq 'REPEAT_LIST' ) {
} elsif( $name eq 'REPEAT' ) {
my ($s,$e) = ($attr->{'{}COORDS'}->{'Value'} =~ /(\d+)\-(\d+)/);
my $strand = 1;
if( $s > $e) {
($s,$e,$strand) = ( $e,$s,-1);
}
my $f = Bio::SeqFeature::Generic->new
(-primary_tag => 'simple_repeat',
-source_tag => $Default_Source,
-seq_id => $seqid,
-start => $s,
-end => $e,
-stand => $strand,
-tag => {
'ID' => $attr->{'{}FEAT_NAME'}->{'Value'},
});
push @{$self->{'_seendata'}->{'_feats'}}, $f;
$self->{'_seendata'}->{'_seqs'}->[-1]->add_SeqFeature($f);
} elsif ( $name eq 'AUTHOR' ) {
} elsif( $name eq 'GB_DESCRIPTION' ) {
} elsif( $name eq 'GB_COMMENT' ) {
} elsif( $name eq 'LINEAGE' ) {
} else {
$self->warn("Unknown element $name, ignored\n");
}
push @{$self->{'_state'}}, $name;
$self->SUPER::start_element($ele);
}
sub end_element {
my ($self,$ele) = @_;
pop @{$self->{'_state'}};
my $name = $ele->{'LocalName'};
my $curseq = $self->{'_seendata'}->{'_seqs'}->[-1];
if( $name eq 'AUTHOR_LIST' ) {
if( $curseq->can('annotation') ) {
$curseq->annotation->add_Annotation
('reference',Bio::Annotation::Reference->new
(-authors => join(',',@{$self->{'_seendata'}->{'_authors'}}))
);
}
$self->{'_seendata'}->{'_authors'} = [];
} elsif( $name eq 'ASSEMBLY' ) {
if( @{$self->{'_seendata'}->{'_feats'} || []} ) {
$self->warn("Leftover features which were not finished!");
}
$self->debug("end element for ASSEMBLY ". $curseq->display_id. "\n");
} elsif( $name eq 'TU' ||
$name eq 'TRNA' || $name eq 'PRE-TRNA' ||
$name eq 'REPEAT' ) {
pop @{$self->{'_seendata'}->{'_feats'}};
} elsif( $name eq 'MODEL' ) {
# This is all to for adding UTRs
my $model = pop @{$self->{'_seendata'}->{'_feats'}};
my $curseq = $self->{'_seendata'}->{'_seqs'}->[-1];
# sort smallest to largest, don't forget about
# strandedness
my ($parentid) = $model->get_tag_values('Parent');
my @features = $model->get_SeqFeatures();
my @exons = sort { $a->start <=> $b->start }
grep { $_->primary_tag eq 'exon' } @features;
my @cdsexons = sort { $a->start <=> $b->start }
grep { $_->primary_tag eq 'CDS' } @features;
# look at the exons, find those which come after the model start
my $cdsexon = shift @cdsexons;
my $exon = shift @exons; # first exon
if( ! defined $cdsexon ) {
$self->warn( "no CDS exons $parentid!");
return;
} elsif( ! defined $exon ) {
$self->warn("no exons $parentid!" );
return;
}
my $utrct = 1;
while( defined $exon && $exon->start < $cdsexon->start ) {
my ($pid) = $exon->get_tag_values('Parent');
$self->debug("LeftPhase: tu-id $parentid mrna-id $pid exon is ".
$exon->location->to_FTstring.
" CDSexon is ".$cdsexon->location->to_FTstring."\n");
my $utr = Bio::SeqFeature::Generic->new
(-seq_id => $exon->seq_id,
-strand => $exon->strand,
-primary_tag => $exon->strand > 0 ? "five_prime_UTR" : "three_prime_UTR",
-source_tag => $Default_Source,
-tag => {
'ID' => "$pid.UTR".$utrct++,
'Parent' => $pid },
);
my ($ns,$ne);
if( $utr->primary_tag eq 'five_prime_UTR' ) {
$ns = $exon->start;
$ne = min ( $exon->end, $cdsexon->start - 1);
} else {
$ne = min( $exon->end, $cdsexon->start - 1);
$ns = $exon->start;
}
$utr->start($ns); $utr->end($ne);
$model->add_SeqFeature($utr);
$curseq->add_SeqFeature($utr);
$exon = shift @exons;
}
@exons = sort { $a->start <=> $b->start }
grep {$_->primary_tag eq 'exon' } @features;
@cdsexons = sort { $a->start <=> $b->start }
grep { $_->primary_tag eq 'CDS' } @features;
$cdsexon = pop @cdsexons;
$exon = pop @exons;
if( ! defined $cdsexon ) {
$self->warn( "no CDS exons $parentid!");
return;
} elsif( ! defined $exon ) {
$self->warn("no exons $parentid!" );
return;
}
$utrct = 1;
while( defined $exon &&$exon->end > $cdsexon->end ) {
my ($pid) = $exon->get_tag_values('Parent');
$self->debug("RightPhase: tu-id $parentid mrna-id $pid exon is ".
$exon->location->to_FTstring.
" CDSexon is ".$cdsexon->location->to_FTstring."\n");
my $utr = Bio::SeqFeature::Generic->new
(-seq_id => $exon->seq_id,
-strand => $exon->strand,
-primary_tag => $exon->strand < 0 ? "five_prime_UTR" : "three_prime_UTR",
-source_tag => $Default_Source,
-tag => {
'Parent' => $pid,
'ID' => "$pid.UTR".$utrct++,
}
);
my ($ns,$ne);
if( $utr->primary_tag eq 'three_prime_UTR' ) {
$ns = max ( $exon->start, $cdsexon->end + 1);
$ne = $exon->end;
} else {
$ns = $cdsexon->end+1;
$ne = max ( $exon->end, $cdsexon->start + 1);
}
$utr->start($ns); $utr->end($ne);
$model->add_SeqFeature($utr);
$curseq->add_SeqFeature($utr);
$exon = pop @exons;
}
}
$self->SUPER::end_element($ele);
}
sub characters {
my ($self,$data) = @_;
if( ! @{$self->{'_state'}} ) {
$self->warn("Calling characters with no previous start_element call. Ignoring data");
} else {
my $curseq = $self->{'_seendata'}->{'_seqs'}->[-1];
my $curfeat = $self->{'_seendata'}->{'_feats'}->[-1];
my $name = $self->{'_state'}->[-1];
if( defined $curseq ) {
if( $name eq 'CLONE_NAME' ) {
$self->debug("Clone name is ",$data->{'Data'}, "\n");
$curseq->display_id($data->{'Data'});
} elsif( $name eq 'ORGANISM' ) {
my ($genus,$species,$subspec) = split(/\s+/,$data->{Data},3);
$curseq->species(Bio::Species->new(
-classification =>
[$species,$genus],
-sub_species => $species));
} elsif( $name eq 'LINEAGE' ) {
$curseq->species->classification(
[
$curseq->species->species,
$curseq->species->genus,
reverse (map { s/^\s+//;
s/\s+$//; $_; }
split /[;\.]+/,$data->{'Data'} ),
]
);
} elsif( $name eq 'AUTHOR' ) {
push @{$self->{'_seendata'}->{'_authors'}}, $data->{'Data'};
}
}
if( defined $curfeat ) {
if( $name eq 'EXON' ) { # exon feature
} elsif( $name eq 'RNA-EXON' ) {
} elsif( $name eq 'PROTEIN_SEQ' ) {
$curfeat->add_tag_value('translation',$data->{'Data'});
} elsif( $name eq 'CDS' ) {
} elsif( $name eq 'PRE-TRNA' ) { # tRNA gene
} elsif( $name eq 'TRNA' ) { # tRNA transcript
} elsif( $name eq 'REPEAT_LIST' ) {
} elsif( $name eq 'REPEAT' ) {
$curfeat->add_tag_value('Note',$data->{'Data'});
} elsif( $name eq 'GB_COMMENT' ) {
$curseq->annotation->add_Annotation
('comment',
Bio::Annotation::Comment->new(-text => $data->{'Data'}));
} elsif( $name eq 'GB_DESCRIPTION' ) {
$curseq->description($data->{'Data'});
}
}
}
$self->SUPER::characters($data);
}
sub assert {
my ($self,$test,$msg) = @_;
$self->throw($msg) unless $test;
}
1;