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Downstream.pm
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Downstream.pm
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=head1 LICENSE
Copyright [1999-2015] Wellcome Trust Sanger Institute and the EMBL-European Bioinformatics Institute
Copyright [2016-2018] EMBL-European Bioinformatics Institute
Licensed under the Apache License, Version 2.0 (the "License");
you may not use this file except in compliance with the License.
You may obtain a copy of the License at
http://www.apache.org/licenses/LICENSE-2.0
Unless required by applicable law or agreed to in writing, software
distributed under the License is distributed on an "AS IS" BASIS,
WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied.
See the License for the specific language governing permissions and
limitations under the License.
=head1 CONTACT
Ensembl <http://www.ensembl.org/info/about/contact/index.html>
=cut
=head1 NAME
Downstream
=head1 SYNOPSIS
mv Downstream.pm ~/.vep/Plugins
./vep -i variations.vcf --plugin Downstream
=head1 DESCRIPTION
This is a plugin for the Ensembl Variant Effect Predictor (VEP) that
predicts the downstream effects of a frameshift variant on the protein
sequence of a transcript. It provides the predicted downstream protein
sequence (including any amino acids overlapped by the variant itself),
and the change in length relative to the reference protein.
Note that changes in splicing are not predicted - only the existing
translateable (i.e. spliced) sequence is used as a source of
translation. Any variants with a splice site consequence type are
ignored.
=cut
package Downstream;
use strict;
use warnings;
use Bio::EnsEMBL::Variation::Utils::BaseVepPlugin;
use POSIX qw(ceil);
use base qw(Bio::EnsEMBL::Variation::Utils::BaseVepPlugin);
sub version {
return '2.3';
}
sub feature_types {
return ['Transcript'];
}
sub variant_feature_types {
return ['VariationFeature'];
}
sub get_header_info {
return {
DownstreamProtein => "Predicted downstream translation for frameshift mutations",
ProteinLengthChange => "Predicted change in protein product length",
};
}
sub run {
my ($self, $tva) = @_;
my @ocs = @{$tva->get_all_OverlapConsequences};
if(grep {$_->SO_term eq 'frameshift_variant'} @ocs) {
# can't do it for splice sites
return {} if grep {$_->SO_term =~ /splice/} @ocs;
my $tv = $tva->transcript_variation;
my $tr = $tv->transcript;
my $cds_seq = defined($tr->{_variation_effect_feature_cache}) ? $tr->{_variation_effect_feature_cache}->{translateable_seq} : $tr->translateable_seq;
# get the sequence to translate
my ($low_pos, $high_pos) = sort {$a <=> $b} ($tv->cds_start, $tv->cds_end);
my $is_insertion = $tv->cds_start > $tv->cds_end ? 1 : 0;
my $last_complete_codon = (ceil($low_pos / 3) - 1) * 3;
my $before_var_seq = substr $cds_seq, $last_complete_codon, $low_pos - $last_complete_codon - ($is_insertion ? 0 : 1);
my $after_var_seq = substr $cds_seq, $high_pos - ($is_insertion ? 1 : 0);
my $to_translate = $before_var_seq.$tva->feature_seq.$after_var_seq;
my $three_prime_utr_seq = $tr->three_prime_utr->seq() if ($tr->three_prime_utr);
$to_translate = $to_translate.$three_prime_utr_seq if ($three_prime_utr_seq);
$to_translate =~ s/\-//g;
# create a bioperl object
my $codon_seq = Bio::Seq->new(
-seq => $to_translate,
-moltype => 'dna',
-alphabet => 'dna'
);
# get codon table
my $codon_table;
if(defined($tr->{_variation_effect_feature_cache})) {
$codon_table = $tr->{_variation_effect_feature_cache}->{codon_table} || 1;
}
else {
my ($attrib) = @{$tr->slice->get_all_Attributes('codon_table')};
$codon_table = $attrib ? $attrib->value || 1 : 1;
}
# translate
my $new_pep = $codon_seq->translate(undef, undef, undef, $codon_table)->seq();
$new_pep =~ s/\*.*//;
# compare lengths
my $translation = defined($tr->{_variation_effect_feature_cache}) && defined($tr->{_variation_effect_feature_cache}->{peptide}) ? $tr->{_variation_effect_feature_cache}->{peptide} : $tr->translation->seq;
my $new_length = ($tv->translation_start < $tv->translation_end ? $tv->translation_start : $tv->translation_end) + length($new_pep);
return {
DownstreamProtein => $new_pep,
ProteinLengthChange => $new_length - length($translation),
};
}
return {};
}
1;