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Copy pathSNPtable2hiestSW_bychr.pl
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SNPtable2hiestSW_bychr.pl
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#!/usr/bin/perl
#This version of the script divides the data into chromosomes. It also requires that an individual have data in atleast 10 sites within a window, or it doesn't print that sample.
use strict;
use warnings;
use lib '/home/owens/bin/pop_gen/'; #For GObox server
my %t;
$t{"N"} = "NN";
$t{"A"} = "AA";
$t{"T"} = "TT";
$t{"G"} = "GG";
$t{"C"} = "CC";
$t{"W"} = "TA";
$t{"R"} = "AG";
$t{"M"} = "AC";
$t{"S"} = "CG";
$t{"K"} = "TG";
$t{"Y"} = "CT";
my $in = $ARGV[0];
my $pop = $ARGV[1];
my $out = $ARGV[2];
require "countbadcolumns.pl";
my ($iupac_coding, $badcolumns) = count_bad_columns($in);
$. = 0;
my %sample;
my $loci_count = 0;
my %data;
my @samplelist;
my %marker;
my %poplist;
my %totals;
my @parents = ("P1", "P2");
my %Major;
my %Minor;
open POP, $pop;
while (<POP>){
chomp;
my @a = split(/\t/, $_);
$poplist{$a[0]} = $a[1];
}
close POP;
my $currentchr;
my %hasdatacount;
open IN, $in;
while (<IN>){
chomp;
my @a = split(/\t/, $_);
if ($. == 1){
foreach my $i ($badcolumns..$#a){
$sample{$i} = $a[$i];
push (@samplelist, $a[$i]);
}
}else{
next if /^\s*$/;
next if /^scaffold/;
unless ($currentchr){
$currentchr = $a[0];
}
my %total_alleles;
# $loci_count++;
if ($currentchr ne $a[0]){
open(my $g_file, '>', "${out}.chr.${currentchr}.hiest.G");
open(my $p_file, '>', "${out}.chr.${currentchr}.hiest.P");
print $g_file "sample";
foreach my $i (1..$loci_count){
print $g_file "\t$marker{$i}";
}
foreach my $sample (@samplelist){
if ($poplist{$sample} eq "H"){
if ($hasdatacount{$sample}){
if ($hasdatacount{$sample} >= 10){
print $g_file "\n";
print $g_file "$sample";
foreach my $i (1..$loci_count){
print $g_file "\t$data{$sample}{$i}";
}
}
}
}
}
close $g_file;
print $p_file "Locus\tAllele\tP1\tP2";
foreach my $i (1..$loci_count){
print $p_file "\n";
print $p_file "$marker{$i}\t1";
foreach my $pop (@parents){
my $freq;
if (($totals{$i}{$pop}{$Major{$i}}) and ($totals{$i}{$pop}{$Minor{$i}})){
$freq = ($totals{$i}{$pop}{$Major{$i}} / ($totals{$i}{$pop}{$Major{$i}} + $totals{$i}{$pop}{$Minor{$i}}));
}elsif($totals{$i}{$pop}{$Major{$i}}){
$freq = "1";
}else{
$freq = "0";
}
print $p_file "\t$freq";
}
}
close $p_file;
#Reset the variables
$currentchr = $a[0];
%totals = ();
$loci_count = 0;
%data= ();
%marker = ();
%hasdatacount = ();
}
$loci_count++;
$marker{$loci_count} = "$a[0]_$a[1]";
foreach my $i ($badcolumns..$#a){
if ($iupac_coding eq "TRUE"){
$a[$i] = $t{$a[$i]};
}
unless (($a[$i] eq "NN")or($a[$i] eq "XX")){
$hasdatacount{$sample{$i}}++;
my @strands = split(//, $a[$i]);
$total_alleles{$strands[0]}++;
$total_alleles{$strands[1]}++;
if ($poplist{$sample{$i}} ne "H"){
$totals{$loci_count}{$poplist{$sample{$i}}}{$strands[0]}++;
$totals{$loci_count}{$poplist{$sample{$i}}}{$strands[1]}++;
}
}
}
# print "$totals{$loci_count}{'P1'}{'A'}\n";
my @bases = sort { $total_alleles{$a} <=> $total_alleles{$b} } keys %total_alleles ;
$Major{$loci_count} = $bases[1];
$Minor{$loci_count} = $bases[0];
foreach my $i ($badcolumns..$#a){
my @strands = split(//, $a[$i]);
if ($strands[0] eq "N"){
$data{$sample{$i}}{$loci_count} = "-9";
}elsif(($strands[0] eq $bases[0]) and ($strands[1] eq $bases[0])){
$data{$sample{$i}}{$loci_count} = "0";
}elsif ($strands[0] ne $strands[1]){
$data{$sample{$i}}{$loci_count} = "1";
}else{
$data{$sample{$i}}{$loci_count} = "2";
}
}
}
}