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CAPICE.pm
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CAPICE.pm
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=head1 LICENSE
Copyright [1999-2015] Wellcome Trust Sanger Institute and the EMBL-European Bioinformatics Institute
Copyright [2016-2024] 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
CAPICE
=head1 SYNOPSIS
mv CAPICE.pm ~/.vep/Plugins
# Download CAPICE SNVs, InDels and index (TBI) files to the same path
# - capice_v1.0_build37_indels.tsv.gz
# - capice_v1.0_build37_indels.tsv.gz.tbi
# - capice_v1.0_build37_snvs.tsv.gz
# - capice_v1.0_build37_snvs.tsv.gz.tbi
./vep -i variations.vcf --plugin CAPICE,snv=/FULL_PATH_TO_CAPICE_FILE/capice_v1.0_build37_snvs.tsv.gz,indels=/FULL_PATH_TO_CAPICE_FILE/capice_v1.0_build37_indels.tsv.gz
./filter_vep -i variant_effect_output.txt --filter "CAPICE_SCORE >= 0.02"
=head1 DESCRIPTION
A VEP plugin that retrieves CAPICE scores for variants from one or more
tabix-indexed CAPICE data files, in order to predict their pathogenicity.
Please cite the CAPICE publication alongside the VEP if you use this resource:
https://pubmed.ncbi.nlm.nih.gov/32831124/
The tabix utility must be installed in your path to use this plugin. The CAPICE
SNVs, InDels and respective index (TBI) files for GRCh37 can be downloaded from
https://zenodo.org/record/3928295
To filter results, please use filter_vep with the output file or standard
output. Documentation on filter_vep is available at:
https://www.ensembl.org/info/docs/tools/vep/script/vep_filter.html
For recommendations on threshold selection, please read the CAPICE publication.
=cut
package CAPICE;
use strict;
use warnings;
use Bio::EnsEMBL::Utils::Sequence qw(reverse_comp);
use Bio::EnsEMBL::Variation::Utils::Sequence qw(get_matched_variant_alleles);
use Bio::EnsEMBL::Variation::Utils::BaseVepTabixPlugin;
use base qw(Bio::EnsEMBL::Variation::Utils::BaseVepTabixPlugin);
sub new {
my $class = shift;
my $self = $class->SUPER::new(@_);
$self->expand_left(0);
$self->expand_right(0);
$self->get_user_params();
# Check files in arguments
my @files;
my $params = $self->params_to_hash();
if (!keys %$params){
@files = @{$self->params};
} else {
for my $key (keys %{$params}) {
push @files, $params->{$key};
}
}
die "ERROR: No CAPICE files specified\n" unless @files > 0;
$self->add_file($_) for @files;
return $self;
}
sub feature_types {
return ['Feature','Intergenic'];
}
sub get_header_info {
return {
CAPICE_SCORE => 'CAPICE score to predict the pathogenicity of SNVs and InDels'
}
}
sub run {
my ($self, $tva) = @_;
my $vf = $tva->variation_feature;
# get allele
my $allele = $tva->base_variation_feature->alt_alleles;
my @data = @{$self->get_data($vf->{chr}, $vf->{start} - 2, $vf->{end})};
foreach (@data) {
my $matches = get_matched_variant_alleles(
{
ref => $vf->ref_allele_string,
alts => $allele,
pos => $vf->{start},
strand => $vf->strand
},
{
ref => $_->{ref},
alts => [$_->{alt}],
pos => $_->{start},
}
);
return $_->{result} if (@$matches);
}
return {};
}
sub parse_data {
my ($self, $line) = @_;
my ($chrom, $start, $ref, $alt, $score) = split /\t/, $line;
# VCF-like adjustment of mismatched substitutions for comparison with VEP
if(length($alt) != length($ref)) {
my $first_ref = substr($ref, 0, 1);
my $first_alt = substr($alt, 0, 1);
if ($first_ref eq $first_alt) {
$start++;
$ref = substr($ref, 1);
$alt = substr($alt, 1);
$ref ||= '-';
$alt ||= '-';
}
}
return {
ref => $ref,
alt => $alt,
start => $start,
result => {
CAPICE_SCORE => $score
}
};
}
sub get_start {
return $_[1]->{start};
}
sub get_end {
return $_[1]->{end};
}
1;