/usr/bin/vcf-subset is in vcftools 0.1.15-1.
This file is owned by root:root, with mode 0o755.
The actual contents of the file can be viewed below.
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 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149 150 151 152 153 154 155 156 157 158 159 160 161 162 163 164 165 166 167 168 169 170 171 172 173 174 175 176 177 178 179 180 181 182 183 184 185 186 187 188 189 190 191 192 193 194 195 196 197 198 199 200 201 202 203 204 205 206 207 208 209 210 211 212 213 214 215 216 217 218 219 220 221 222 223 | #!/usr/bin/env perl
#
# Author: petr.danecek@sanger
#
use strict;
use warnings;
use Carp;
use Vcf;
my $opts = parse_params();
vcf_subset($opts);
exit;
#--------------------------------
sub error
{
my (@msg) = @_;
if ( scalar @msg )
{
croak @msg;
}
die
"Usage: vcf-subset [OPTIONS] in.vcf.gz > out.vcf\n",
"Options:\n",
" -a, --trim-alt-alleles Remove alternate alleles if not found in the subset\n",
" -c, --columns <string> File or comma-separated list of columns to keep in the vcf file. If file, one column per row\n",
" -e, --exclude-ref Exclude rows not containing variants.\n",
" -f, --force Proceed anyway even if VCF does not contain some of the samples.\n",
" -p, --private Print only rows where only the subset columns carry an alternate allele.\n",
" -r, --replace-with-ref Replace the excluded types with reference allele instead of dot.\n",
" -t, --type <list> Comma-separated list of variant types to include: ref,SNPs,indels,MNPs,other.\n",
" -u, --keep-uncalled Do not exclude rows without calls.\n",
" -h, -?, --help This help message.\n",
"Examples:\n",
" cat in.vcf | vcf-subset -r -t indels -e -c SAMPLE1 > out.vcf\n",
"\n";
}
sub parse_params
{
$0 =~ s{^.+/}{}; $0 .= "($Vcf::VERSION)";
my $opts = { exclude_ref=>0, keep_uncalled=>0, replace_with_ref=>0, private=>0, args=>[$0, @ARGV] };
while (my $arg=shift(@ARGV))
{
if ( $arg eq '-t' || $arg eq '--type' )
{
my %known = ( ref=>'r', SNPs=>'s', indels=>'i', MNPs=>'m', other=>'o' );
my $types = shift(@ARGV);
for my $t (split(/,/,$types))
{
if ( !(exists($known{$t})) ) { error("Unknown type [$t] with -t [$types]\n"); }
$$opts{types}{$known{$t}} = 1;
}
next;
}
if ( $arg eq '-a' || $arg eq '--trim-alt-alleles' ) { $$opts{'trim_alts'} = 1; next }
if ( $arg eq '-e' || $arg eq '--exclude-ref' ) { $$opts{'exclude_ref'} = 1; next }
if ( $arg eq '-f' || $arg eq '--force' ) { $$opts{'force'} = 1; next }
if ( $arg eq '-p' || $arg eq '--private' ) { $$opts{'private'} = 1; next }
if ( $arg eq '-r' || $arg eq '--replace-with-ref' ) { $$opts{'replace_with_ref'} = 1; next }
if ( $arg eq '-u' || $arg eq '--keep-uncalled' ) { $$opts{'keep_uncalled'} = 1; next }
if ( $arg eq '-c' || $arg eq '--columns' ) { $$opts{'columns_file'} = shift(@ARGV); next }
if ( $arg eq '-?' || $arg eq '-h' || $arg eq '--help' ) { error(); }
if ( -e $arg ) { $$opts{file} = $arg; next }
if ( -e $arg or $arg=~m{^(?:ftp|http)://} ) { $$opts{file}=$arg; next; }
error("Unknown parameter \"$arg\". Run -h for help.\n");
}
if ( !$$opts{exclude_ref} && !$$opts{'columns_file'} && !exists($$opts{'types'}) && !exists($$opts{trim_alts}) ) { error("Missing the -c or -t or -r option.\n") }
return $opts;
}
sub read_columns
{
my ($fname) = @_;
my @columns;
if ( !-e $fname )
{
@columns = split(/,/,$fname);
return \@columns;
}
open(my $fh,'<',$fname) or error("$fname: $!");
while (my $line=<$fh>)
{
chomp($line);
$line=~s/\s+//g;
push @columns, $line;
}
close($fh);
return \@columns;
}
sub check_columns
{
my ($opts,$vcf,$columns) = @_;
my @out;
for my $col (@$columns)
{
if ( exists($$vcf{has_column}{$col}) )
{
push @out, $col;
next;
}
my $msg = qq[No such column in the VCF file: "$col"\n];
if ( $$opts{force} ) { warn($msg); }
else { error($msg); }
}
return \@out;
}
sub vcf_subset
{
my ($opts) = @_;
my $vcf = $$opts{file} ? Vcf->new(file=>$$opts{file}) : Vcf->new(fh=>\*STDIN);
$vcf->parse_header();
my $AGtags;
if ( $$opts{trim_alts} )
{
$$vcf{trim_redundant_ALTs} = 1;
$AGtags = $vcf->has_AGtags();
}
# Init requested column info. If not present, include all columns.
my $columns = exists($$opts{columns_file}) ? read_columns($$opts{columns_file}) : [];
$columns = check_columns($opts,$vcf,$columns);
if ( !@$columns && (my $ncols=@{$$vcf{columns}})>9 )
{
push @$columns, @{$$vcf{columns}}[9..($ncols-1)];
}
my $columns_to_keep = { map { $_ => 1 } @$columns };
my %has_col = map { $_ => 1 } @$columns;
$vcf->add_header_line({key=>'source',value=>join(' ',@{$$opts{args}})},append=>'timestamp');
$vcf->set_samples(include=>$columns) unless $$opts{private};
print $vcf->format_header($columns);
my $check_private = $$opts{private};
while (my $x=$vcf->next_data_hash())
{
my $site_has_call = 0;
my $site_has_nonref = 0;
my $site_is_private = 1;
my $ref = $$x{REF};
for my $col (keys %{$$x{gtypes}})
{
if ( !$has_col{$col} && ($site_is_private==0 || !$check_private) )
{
# This column is not to be printed
delete($$x{gtypes}{$col});
next;
}
my ($alleles,$seps,$is_phased,$is_empty) = $vcf->parse_haplotype($x,$col);
my $sample_has_call = 0;
my $sample_has_nonref = 0;
my @out_alleles;
for (my $i=0; $i<@$alleles; $i++)
{
my ($type,$len,$ht) = $vcf->event_type($ref,$$alleles[$i]);
$out_alleles[$i] = $$alleles[$i];
# Exclude unwanted variant types if requested
if ( exists($$opts{types}) )
{
if ( $type eq 's' && $len>1 ) { $type = 'm'; }
elsif ( $type eq 'b' or $type eq 'u' ) { $type = 'o'; }
if ( !exists($$opts{types}{$type}) )
{
$out_alleles[$i] = $$opts{replace_with_ref} ? $ref : '.';
next;
}
$sample_has_call = 1;
}
elsif ( !$is_empty ) { $sample_has_call = 1; }
if ( $type ne 'r' ) { $site_has_nonref = 1; $sample_has_nonref = 1; }
}
if ( $check_private && !$has_col{$col} )
{
if ( $sample_has_nonref ) { $site_is_private=0; }
delete($$x{gtypes}{$col});
next;
}
if ( !$sample_has_call )
{
if ( $$opts{replace_with_ref} )
{
for (my $i=0; $i<@$alleles; $i++) { $out_alleles[$i] = $ref; }
}
else
{
for (my $i=0; $i<@$alleles; $i++) { $out_alleles[$i] = '.'; }
}
}
else
{
$site_has_call = 1;
}
$$x{gtypes}{$col}{GT} = $vcf->format_haplotype(\@out_alleles,$seps);
}
if ( !$site_has_call && !$$opts{keep_uncalled} ) { next; }
if ( !$site_has_nonref && $$opts{exclude_ref} ) { next; }
if ( $check_private && (!$site_is_private || !$site_has_nonref) ) { next; }
if ( $$opts{trim_alts} && defined $AGtags )
{
$vcf->remove_columns($x, keep=>$columns_to_keep);
$vcf->parse_AGtags($x);
}
$vcf->format_genotype_strings($x);
print $vcf->format_line($x,$columns);
}
}
|