This file is indexed.

/usr/bin/fill-aa is in vcftools 0.1.12+dfsg-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
#!/usr/bin/env perl
#
# Notes:
#   * The AA files can be downloaded from ftp://ftp.1000genomes.ebi.ac.uk/vol1/ftp/pilot_data/technical/reference/ancestral_alignments
#   * The program runs samtools, therefore the AA files must be gzipped (not b2zipped).
#
# support: pd3@sanger

use strict;
use warnings;
use Carp;
use Vcf;
use FindBin;
use lib "$FindBin::Bin";
use FaSlice;

my $opts = parse_params();
fill_aa($opts,$$opts{aa_file});

exit;

#--------------------------------

sub error
{
    my (@msg) = @_;
    if ( scalar @msg ) { confess @msg; }
    die
        "About: This script fills ancestral alleles into INFO column of VCF files. It depends on samtools,\n",
        "   therefore the fasta sequence must be gzipped (not bgzipped!) and indexed by samtools faidx.\n",
        "   The AA files can be downloaded from\n",
        "       ftp://ftp.1000genomes.ebi.ac.uk/vol1/ftp/pilot_data/technical/reference/ancestral_alignments\n",
        "   and processed as shown in the example below. This is because the sequences in the original files\n",
        "   are named as 'ANCESTOR_for_chromosome:NCBI36:1:1:247249719', but the underlying FaSplice.pm\n",
        "   requires names as 'chr1' or '1'.\n",
        "Usage: fill-aa [OPTIONS] < in.vcf >out.vcf\n",
        "Options:\n",
        "   -a, --ancestral-allele <prefix>     Prefix to ancestral allele chromosome files.\n",
        "   -t, --type <list>                   Variant types to process: all,indel,ref,snp. [all]\n",
        "   -h, -?, --help                      This help message.\n",
        "Example:\n",
        "   # Get the files ready: compress by gzip and index by samtools faidx. Either repeat the\n",
        "   # following command for each file manually\n",
        "   bzcat human_ancestor_1.fa.bz2 | sed 's,^>.*,>1,' | gzip -c > human_ancestor_1.fa.gz\n",
        "   samtools faidx human_ancestor_1.fa.gz\n",
        "   \n",
        "   # .. or use this loop (tested in bash shell)\n",
        "   ls human_ancestor_*.fa.bz2 | while read IN; do\n",
        "       OUT=`echo \$IN | sed 's,bz2\$,gz,'`\n",
        "       CHR=`echo \$IN | sed 's,human_ancestor_,, ; s,.fa.bz2,,'`\n",
        "       bzcat \$IN | sed \"s,^>.*,>\$CHR,\" | gzip -c > \$OUT\n",
        "       samtools faidx \$OUT\n",
        "   done\n",
        "   \n",
        "   # After this has been done, the following command should return 'TACGTGGcTGCTCTCACACAT'\n",
        "   samtools faidx human_ancestor_1.fa.gz 1:1000000-1000020\n",
        "   \n",
        "   # Now the files are ready to use with fill-aa. Note that the VCF file\n",
        "   # should be sorted (see vcf-sort), otherwise the performance would be seriously\n",
        "   # affected.\n",
        "   cat file.vcf | fill-aa -a human_ancestor_ 2>test.err | gzip -c >out.vcf.gz \n",
        "\n";
}


sub parse_params
{
    my $opts = {};
    while (my $arg=shift(@ARGV))
    {
        if ( $arg eq '-a' || $arg eq '--ancestral-allele' ) { $$opts{aa_file} = shift(@ARGV); next }
        if ( $arg eq '-t' || $arg eq '--type' ) 
        { 
            my %known = ( snp=>'s', indel=>'i', all=>'a', ref=>'r' );
            my $types = shift(@ARGV);
            for my $t (split(/,/,$types))
            {
                if ( !(exists($known{$t})) ) { error("Unknown type [$t] with -t [$types]\n"); }
                $$opts{types}{$known{$t}} = 1;
            }
            if ( exists($$opts{types}{a}) )
            {
                $$opts{types}{s} = 1;
                $$opts{types}{i} = 1;
                $$opts{types}{r} = 1;
            }
            next;
        }
        if ( $arg eq '-?' || $arg eq '-h' || $arg eq '--help' ) { error(); }
        error("Unknown parameter \"$arg\". Run -h for help.\n");
    }
    if ( !exists($$opts{aa_file}) ) { error("Missing the -a option.\n") }
    return $opts;
}


sub fill_aa
{
    my ($opts,$aa_fname) = @_;

    my $n_unknown = 0;
    my $n_filled_sites = 0;
    my $n_filled_bases = 0;

    my $vcf = Vcf->new(fh=>\*STDIN, assume_uppercase=>1);
    $vcf->parse_header();
    $vcf->add_header_line({key=>'INFO',ID=>'AA',Number=>1,Type=>'String',
        Description=>'Ancestral Allele, ftp://ftp.1000genomes.ebi.ac.uk/vol1/ftp/pilot_data/technical/reference/ancestral_alignments/README'});
    print $vcf->format_header();

    my %chr2fa = ();
    my $nskipped = 0;
    while (my $line = $vcf->next_line() )
    {
        my $rec = $vcf->next_data_array($line);
        my $chr = $$rec[0];
        my $pos = $$rec[1];
        my $ref = $$rec[3];

        if ( !exists($chr2fa{$chr}) )
        {
            my $fname = $aa_fname;
            if ( ! -e $fname )
            {
                if ( -e "$fname$chr.fa.gz" ) { $fname = "$fname$chr.fa.gz"; }
                else { error(qq[Neither "$fname" nor "$fname$chr.fa.gz" exists.\n]); }
            }
            $chr2fa{$chr} = FaSlice->new(file=>$fname, size=>100_000);
        }

        my $fa = $chr2fa{$chr};
        my $ref_len = length($ref);
        if ( exists($$opts{types}) && !exists($$opts{types}{a}) )
        {
            my $ok = 0;
            for my $alt (split(/,/,$$rec[4]))
            {
                my ($type,$len,$ht) = $vcf->event_type($ref,$alt);
                if ( exists($$opts{types}{$type}) ) { $ok=1; last; }
            }
            if ( !$ok )
            {
                print $line;
                $nskipped++;
                next;
            }
        }
        my $aa = $ref_len==1 ? $fa->get_base($chr,$pos) : $fa->get_slice($chr,$pos,$pos+$ref_len-1);

        if ( $aa )
        {
            $$rec[7] = $vcf->add_info_field($$rec[7],'AA'=>$aa);
            $n_filled_sites++;
            $n_filled_bases+=$ref_len;
        }
        else
        {
            $$rec[7] = $vcf->add_info_field($$rec[7],'AA'=>'.');
            $n_unknown++;
        }
        print join("\t",@$rec),"\n";
    }

    print STDERR 
        "AA sites filled  .. $n_filled_sites\n",
        "AA bases filled  .. $n_filled_bases\n",
        "No AAs           .. $n_unknown\n",
        "Lines skipped    .. $nskipped\n";
}