Permalink
Find file
Fetching contributors…
Cannot retrieve contributors at this time
161 lines (115 sloc) 4.04 KB
=head1 LICENSE
Copyright [1999-2015] Wellcome Trust Sanger Institute and the EMBL-European Bioinformatics Institute
Copyright [2016-2017] 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 <dev@ensembl.org>
=cut
=head1 NAME
SpliceRegion
=head1 SYNOPSIS
mv SpliceRegion.pm ~/.vep/Plugins
./vep -i variations.vcf --plugin SpliceRegion
=head1 DESCRIPTION
This is a plugin for the Ensembl Variant Effect Predictor (VEP) that
provides more granular predictions of splicing effects.
Three additional terms may be added:
# splice_donor_5th_base_variant : variant falls in the 5th base after the splice donor junction (5' end of intron)
v
...EEEEEIIIIIIIIII...
(E = exon, I = intron, v = variant location)
# splice_donor_region_variant : variant falls in region between 3rd and 6th base after splice junction (5' end of intron)
vv vvv
...EEEEEIIIIIIIIII...
# splice_polypyrimidine_tract_variant : variant falls in polypyrimidine tract at 3' end of intron, between 17 and 3 bases from the end
vvvvvvvvvvvvvvv
...IIIIIIIIIIIIIIIIIIIIEEEEE...
=cut
package SpliceRegion;
use strict;
use warnings;
use Bio::EnsEMBL::Variation::Utils::VariationEffect qw(overlap);
use Bio::EnsEMBL::Variation::Utils::Constants qw(%OVERLAP_CONSEQUENCES);
use base qw(Bio::EnsEMBL::Variation::Utils::BaseVepPlugin);
my %TERM_RANK = (
splice_donor_5th_base_variant => 1,
splice_donor_region_variant => 2,
splice_polypyrimidine_tract_variant => 3,
);
sub feature_types {
return ['Transcript'];
}
sub get_header_info {
return {
SpliceRegion => "SpliceRegion predictions",
};
}
sub run {
my ($self, $tva) = @_;
my $vf = $tva->variation_feature;
my ($vf_start, $vf_end) = ($vf->{start}, $vf->{end});
my $is_insertion = 0;
if($vf_start > $vf_end) {
($vf_start, $vf_end) = ($vf_end, $vf_start);
$is_insertion = 1;
}
my $tv = $tva->transcript_variation;
my $tr = $tv->transcript;
my $vf_tr_seq = $tva->feature_seq;
# define some variables depending on transcript strand
my ($strand_mod, $donor_coord, $acc_coord);
if($tr->strand > 0) {
$strand_mod = 1;
$donor_coord = 'start';
$acc_coord = 'end';
}
else {
$strand_mod = -1;
$donor_coord = 'end';
$acc_coord = 'start';
}
my %results;
for my $intron(@{$tv->_overlapped_introns($vf_start, $vf_end)}) {
# define terms to check for and their regions
my @terms = (
{
term => 'splice_donor_5th_base_variant',
region => [$intron->{$donor_coord} + (4 * $strand_mod), $intron->{$donor_coord} + (4 * $strand_mod)]
},
{
term => 'splice_donor_region_variant',
region => [$intron->{$donor_coord} + (2 * $strand_mod), $intron->{$donor_coord} + (5 * $strand_mod)]
},
{
term => 'splice_polypyrimidine_tract_variant',
region => [$intron->{$acc_coord} + (-16 * $strand_mod), $intron->{$acc_coord} + (-2 * $strand_mod)],
# allele_specific_mod => {
# A => '_to_purine',
# G => '_to_purine',
# }
},
);
foreach my $term_hash(@terms) {
my $pass = overlap($vf_start, $vf_end, sort {$a <=> $b} @{$term_hash->{region}});
if($pass) {
my $term = $term_hash->{term};
# if(my $allele_specific_mods = $term_hash->{allele_specific_mod}) {
# $term .= $allele_specific_mods->{$vf_tr_seq} || '';
# }
$results{$term}++;
last;
}
}
}
return {} unless %results;
return { SpliceRegion => [sort {$TERM_RANK{$a} <=> $TERM_RANK{$b}} keys %results]};
}
1;