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| =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 | |
| Will McLaren <wm2@ebi.ac.uk> | |
| =cut | |
| =head1 NAME | |
| FATHMM_MKL | |
| =head1 SYNOPSIS | |
| mv FATHMM_MKL.pm ~/.vep/Plugins | |
| ./vep -i input.vcf --plugin FATHMM_MKL,fathmm-MKL_Current.tab.gz | |
| =head1 DESCRIPTION | |
| A VEP plugin that retrieves FATHMM-MKL scores for variants from a tabix-indexed | |
| FATHMM-MKL data file. | |
| See https://github.com/HAShihab/fathmm-MKL for details. | |
| NB: The currently available data file is for GRCh37 only. | |
| =cut | |
| package FATHMM_MKL; | |
| use strict; | |
| use warnings; | |
| use Bio::EnsEMBL::Utils::Sequence qw(reverse_comp); | |
| 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); | |
| return $self; | |
| } | |
| sub feature_types { | |
| return ['Feature','Intergenic']; | |
| } | |
| sub get_header_info { | |
| my $self = shift; | |
| return { | |
| FATHMM_MKL_C => 'FATHMM-MKL coding score', | |
| FATHMM_MKL_NC => 'FATHMM-MKL non-coding score', | |
| } | |
| } | |
| sub run { | |
| my ($self, $tva) = @_; | |
| my $vf = $tva->variation_feature; | |
| return {} unless $vf->{start} eq $vf->{end}; | |
| # get allele, reverse comp if needed | |
| my $allele = $tva->variation_feature_seq; | |
| reverse_comp(\$allele) if $vf->{strand} < 0; | |
| return {} unless $allele =~ /^[ACGT]$/; | |
| # adjust coords, file is BED-like (but not 0-indexed, go figure...) | |
| my ($s, $e) = ($vf->{start}, $vf->{end} + 1); | |
| foreach my $data(@{$self->get_data($vf->{chr}, $s, $e)}) { | |
| if($data->{start} == $s && $allele eq $data->{alt}) { | |
| return $data->{result}; | |
| } | |
| } | |
| return {}; | |
| } | |
| sub parse_data { | |
| my ($self, $line) = @_; | |
| my ($c, $s, $e, $ref, $alt, $nc_score, $nc_groups, $c_score, $c_groups) = split /\t/, $line; | |
| return { | |
| start => $s, | |
| end => $e - 1, | |
| alt => $alt, | |
| result => { | |
| FATHMM_MKL_C => $c_score, | |
| FATHMM_MKL_NC => $nc_score, | |
| } | |
| }; | |
| } | |
| sub get_start { | |
| return $_[1]->{start}; | |
| } | |
| sub get_end { | |
| return $_[1]->{end}; | |
| } | |
| 1; | |