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1 #!/usr/bin/perl -w
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2 use strict;
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3
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4 #divide the alleles and their information into separate columns for pgSnp-like
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5 #files. Keep any additional columns beyond the pgSnp ones.
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6 #reads from stdin, writes to stdout
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7 my $ref;
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8 my $in;
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9 if (@ARGV && $ARGV[0] =~ /-ref=(\d+)/) {
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10 $ref = $1 -1;
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11 if ($ref == -1) { undef $ref; }
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12 shift @ARGV;
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13 }
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14 if (@ARGV) {
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15 $in = shift @ARGV;
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16 }
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17
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18 open(FH, $in) or die "Couldn't open $in, $!\n";
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19 while (<FH>) {
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20 chomp;
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21 my @f = split(/\t/);
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22 my @a = split(/\//, $f[3]);
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23 my @fr = split(/,/, $f[5]);
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24 my @sc = split(/,/, $f[6]);
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25 if ($f[4] == 1) { #homozygous add N, 0, 0
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26 if ($ref) { push(@a, $f[$ref]); }
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27 else { push(@a, "N"); }
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28 push(@fr, 0);
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29 push(@sc, 0);
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30 }
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31 if ($f[4] > 2) { next; } #skip those with more than 2 alleles
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32 print "$f[0]\t$f[1]\t$f[2]\t$a[0]\t$fr[0]\t$sc[0]\t$a[1]\t$fr[1]\t$sc[1]";
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33 if (scalar @f > 7) {
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34 splice(@f, 0, 7); #remove first 7
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35 print "\t", join("\t", @f), "\n";
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36 }else { print "\n"; }
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37 }
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38 close FH;
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39
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40 exit;
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41
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