forked from Ensembl/VEP_plugins
-
Notifications
You must be signed in to change notification settings - Fork 0
/
gnomADc.pm
195 lines (127 loc) · 4.74 KB
/
gnomADc.pm
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
121
122
123
124
125
126
127
128
129
130
131
132
133
134
135
136
137
138
139
140
141
142
143
144
145
146
147
148
149
150
151
152
153
154
155
156
157
158
159
160
161
162
163
164
165
166
167
168
169
170
171
172
173
174
175
176
177
178
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
194
=head1 LICENSE
Copyright 2018 QIMR Berghofer Medical Research 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
Stephen Kazakoff <[email protected]>
=cut
=head1 NAME
gnomADc
=head1 SYNOPSIS
mv gnomADc.pm ~/.vep/Plugins
./vep -i variations.vcf --plugin gnomADc,/path/to/gnomad-public/r2.0.2/coverage/genomes
./vep -i variations.vcf --plugin gnomADc,/path/to/gnomad-public/r2.0.2/coverage/exomes
=head1 DESCRIPTION
A VEP plugin that retrieves gnomAD annotation from either the genome
or exome coverage files, available here:
http://gnomad.broadinstitute.org/downloads
The coverage files must be downloaded and tabix indexed before using this
plugin:
> release="2.0.2"
> genomes="https://storage.googleapis.com/gnomad-public/release/${release}/coverage/genomes"
> wget -x "${genomes}"/gnomad.genomes.r${release}.chr{{1..22},X}.coverage.txt.gz
> for i in "${genomes#*//}"/gnomad.genomes.r${release}.chr{{1..22},X}.coverage.txt.gz; do
> tabix -s 1 -b 2 -e 2 "${i}"
> done
> exomes="https://storage.googleapis.com/gnomad-public/release/${release}/coverage/exomes"
> wget -x "${exomes}"/gnomad.exomes.r${release}.chr{{1..22},X,Y}.coverage.txt.gz
> for i in "${exomes#*//}"/gnomad.exomes.r${release}.chr{{1..22},X,Y}.coverage.txt.gz; do
> tabix -s 1 -b 2 -e 2 "${i}"
> done
The parent directory's basename is used to set the output field prefix. This
is 'gnomADg' for genomes, 'gnomADe' for exomes, or else just 'gnomAD'.
If you use this plugin, please see the terms and data information:
http://gnomad.broadinstitute.org/terms
The gnomAD coverage files are provided for GRCh37, but if you use GRCh38
you may like to use the liftover files, available here:
https://console.cloud.google.com/storage/browser/gnomad-public/release
You must have the Bio::DB::HTS module or the tabix utility must be installed
in your path to use this plugin.
=cut
package gnomADc;
use strict;
use warnings;
use File::Basename;
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();
my $params = $self->params;
my $dir = shift @$params;
die("ERROR: gnomAD directory not specified\n") unless $dir;
die("ERROR: gnomAD directory not found\n") unless -d $dir;
# use the parent directory's basename to set a column prefix
my $base = basename($dir);
my $prefix = 'gnomAD' . ($base eq 'genomes' || $base eq 'exomes' ? substr($base, 0, 1) : '');
# add any coverage files to our list of inputs
opendir (my $fh, $dir) or die $!;
for (readdir $fh) {
$self->add_file("$dir/$_") if /\.coverage\.txt\.gz$/;
}
closedir $fh;
my @files = @{ $self->files() };
die("ERROR: Could not find any $prefix coverage files\n") unless @files;
$self->{prefix} = $prefix;
return $self;
}
sub feature_types {
return ['Feature', 'Intergenic'];
}
sub get_header_info {
my $self = shift;
my $prefix = $self->{prefix};
my %header_info;
for (qw(mean median)) {
$header_info{ join('_', $prefix, $_, 'cov') } = "$_ coverage";
};
for (qw(1x 5x 10x 15x 20x 25x 30x 50x 100x)) {
$header_info{ join('_', $prefix, $_, 'cov') } = "Fraction of samples at $_ coverage";
}
return \%header_info;
}
sub run {
my ($self, $vfoa) = @_;
my $vf = $vfoa->variation_feature;
my ($vf_start, $vf_end) = ($vf->{start}, $vf->{end});
$vf_end = $vf_start if $vf_start > $vf_end;
my @results = @{ $self->get_data($vf->{chr}, $vf_start, $vf_end) };
return {} unless @results;
my %sums;
# sum the values across each position
for my $result (@results) {
$sums{$_} += $result->{$_} for keys %$result;
}
# take the average of each of the values
my %avgs = map { $_ => sprintf("%.4f", $sums{$_} / scalar @results) } keys %sums;
return \%avgs;
}
sub parse_data {
my ($self, $line) = @_;
my $prefix = $self->{prefix};
my ($chr, $pos, @cov) = split /\t/, $line;
my @keys = map {
join('_', $prefix, $_, 'cov')
}
qw(mean median 1x 5x 10x 15x 20x 25x 30x 50x 100x);
my %result;
@result{@keys} = @cov;
return \%result;
}
sub get_start {
return $_[1]->{start};
}
sub get_end {
return $_[1]->{end};
}
1;