0
|
1 #!/usr/bin/perl -w
|
|
2 use strict;
|
|
3
|
|
4 #convert from a vcf file to a pgSnp file.
|
|
5 #frequency count = chromosome count
|
|
6 #either a single column/individual
|
|
7 #or all columns as a population
|
|
8
|
|
9 my $in;
|
|
10 my $stCol = 9;
|
|
11 my $endCol;
|
|
12 if (@ARGV && scalar @ARGV == 2) {
|
|
13 $stCol = shift @ARGV;
|
|
14 $in = shift @ARGV;
|
|
15 if ($stCol eq 'all') { $stCol = 10; }
|
|
16 else { $endCol = $stCol; }
|
|
17 $stCol--; #go from 1 based to zero based column number
|
|
18 if ($stCol < 9) {
|
|
19 print "ERROR genotype fields don't start until column 10\n";
|
|
20 exit;
|
|
21 }
|
|
22 }elsif (@ARGV && scalar @ARGV == 1) {
|
|
23 $in = shift @ARGV;
|
|
24 }elsif (@ARGV) {
|
|
25 print "usage: vcf2pgSnp.pl [indColNum default=all] file.vcf > file.pgSnp\n";
|
|
26 exit;
|
|
27 }
|
|
28
|
|
29 open(FH, $in) or die "Couldn't open $in, $!\n";
|
|
30 while (<FH>) {
|
|
31 chomp;
|
|
32 if (/^\s*#/) { next; } #skip comments/headers
|
|
33 if (/^\s*$/) { next; } #skip blank lines
|
|
34 my @f = split(/\t/);
|
|
35 #chr pos1base ID refNt altNt[,|D#|Int] quality filter info format geno1 ...
|
|
36 my $a;
|
|
37 my %nt;
|
|
38 my %all;
|
|
39 my $cnt = 0;
|
|
40 my $var;
|
|
41 if ($f[3] eq 'N') { next; } #ignore ref=N
|
|
42 if ($f[4] =~ /[DI]/ or $f[3] =~ /[DI]/) { next; } #don't do microsatellite
|
|
43 #if ($f[4] =~ /[ACTG],[ACTG]/) { next; } #only do positions with single alternate
|
|
44 if ($f[6] && !($f[6] eq '.' or $f[6] eq 'PASS')) { next; } #filtered for some reason
|
|
45 my $ind = 0;
|
|
46 if ($f[8] ne 'GT') { #more than just genotype
|
|
47 my @t = split(/:/, $f[8]);
|
|
48 foreach (@t) { if ($_ eq 'GT') { last; } $ind++; }
|
|
49 if ($ind == 0 && $f[8] !~ /^GT/) { die "ERROR couldn't find genotype in format $f[8]\n"; }
|
|
50 }
|
|
51 #count 0's, 1's, 2's
|
|
52 if (!$endCol) { $endCol = $#f; }
|
|
53 foreach my $col ($stCol .. $endCol) {
|
|
54 if ($ind > 0) {
|
|
55 my @t = split(/:/, $f[$col]);
|
|
56 $f[$col] = $t[$ind] . ":"; #only keep genotype part
|
|
57 }
|
|
58 if ($f[$col] =~ /^(0|1|2).(0|1|2)/) {
|
|
59 $nt{$1}++;
|
|
60 $nt{$2}++;
|
|
61 }elsif ($f[$col] =~ /^(0|1|2):/) { #chrY or male chrX, single
|
|
62 $nt{$1}++;
|
|
63 } #else ignore
|
|
64 }
|
|
65 if (%nt) {
|
|
66 if ($f[0] !~ /chr/) { $f[0] = "chr$f[0]"; }
|
|
67 print "$f[0]\t", ($f[1]-1), "\t$f[1]\t"; #position info
|
|
68 my $cnt = scalar(keys %nt);
|
|
69 my $fr;
|
|
70 my $sc;
|
|
71 my $all;
|
|
72 if (exists $nt{0}) {
|
|
73 $all = uc($f[3]);
|
|
74 $fr = $nt{0};
|
|
75 $sc = 0;
|
|
76 }
|
|
77 if (!exists $nt{0} && exists $nt{1}) {
|
|
78 if ($f[4] =~ /([ACTG]),?/) {
|
|
79 $all = $1;
|
|
80 $fr = $nt{1};
|
|
81 $sc = 0;
|
|
82 }else { die "bad variant nt $f[4] for nt 1"; }
|
|
83 }elsif (exists $nt{1}) {
|
|
84 if ($f[4] =~ /([ACTG]),?/) {
|
|
85 $all .= '/' . $1;
|
|
86 $fr .= ",$nt{1}";
|
|
87 $sc .= ",0";
|
|
88 }else { die "bad variant nt $f[4] for nt 1"; }
|
|
89 }
|
|
90 if (exists $nt{2}) {
|
|
91 if ($f[4] =~ /^[ACTG],([ACTG]),?/) {
|
|
92 $all .= '/' . $1;
|
|
93 $fr .= ",$nt{2}";
|
|
94 $sc .= ",0";
|
|
95 }else { die "bad variant nt $f[4] for nt 2"; }
|
|
96 }
|
|
97 if (exists $nt{3}) {
|
|
98 if ($f[4] =~ /^[ACTG],[ACTG],([ACTG])/) {
|
|
99 $all .= '/' . $1;
|
|
100 $fr .= ",$nt{3}";
|
|
101 $sc .= ",0";
|
|
102 }else { die "bad variant nt $f[4] for nt 3"; }
|
|
103 }
|
|
104 if (exists $nt{4}) {
|
|
105 if ($f[4] =~ /^[ACTG],[ACTG],[ACTG],([ACTG])/) {
|
|
106 $all .= '/' . $1;
|
|
107 $fr .= ",$nt{4}";
|
|
108 $sc .= ",0";
|
|
109 }else { die "bad variant nt $f[4] for nt 4"; }
|
|
110 }
|
|
111 print "$all\t$cnt\t$fr\t$sc\n";
|
|
112 }
|
|
113 }
|
|
114 close FH;
|
|
115
|
|
116 exit;
|