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Copy pathSNPtable2BasicPopGenStats_v1.pl
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SNPtable2BasicPopGenStats_v1.pl
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#!/usr/bin/perl
use warnings;
use strict;
use lib './'; #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 %samples;
my @Good_samples;
my %Anc;
my %AncCount;
my %TotalSites;
my %pop;
my %Genotype;
my %samplepop;
my %poplist;
my $Npops = 2;
my $BiCount = 0;
my $TriCount= 0;
my $QuadCount = 0;
my $SingleTri =0;
unless (@ARGV == 2) {die;}
my $in = $ARGV[0];
my $pop = $ARGV[1];
require "countbadcolumns.pl";
my ($iupac_coding, $badcolumns) = count_bad_columns($in);
$. = 0;
open POP, $pop;
while (<POP>){
chomp;
my @a = split (/\t/,$_);
$pop{$a[0]}=$a[1];
$poplist{$a[1]}++;
}
close POP;
my @tmp = keys %poplist;
if ($#tmp eq 2){
print STDERR "This is really only designed for 2 pops, you have $#tmp\n";
}
my $pop1 = $tmp[0];
my $pop2 = $tmp[1];
open IN, $in;
while (<IN>){
chomp;
my @a = split (/\t/,$_);
if ($. == 1){
foreach my $i ($badcolumns..$#a){ #Get sample names for each column
if ($pop{$a[$i]}){
$samplepop{$i} = $pop{$a[$i]};
}
}
print $a[0]."-"."$a[1]\t$a[0]";
foreach my $i (1..($badcolumns-1)){
print "\t$a[$i]";
}
print "\tpAll\tqAll\tHeAll\tHoAll\tCallRate\tp1\tq1\tp2\tq2\tHo1\tHo2\tHe1\tHe2\tFst\tlnRH\tprivate1\tprivate2\tprivatepresent1\tprivatepresent2\tFis1\tFis2\tshared\tdxy\tHsBar\tfixedDif\tn_1\tn_2\tH_bar\tsigma_squared\tWC_a\tWC_b\tWC_c\tWC_fst\tpi\n";
}
else{
next if /^\s*$/;
print $a[0]."-"."$a[1]\t$a[0]";
foreach my $i (1..($badcolumns-1)){
print "\t$a[$i]";
}
my %BC;
my %BS;
my %total_alleles;
foreach my $i ($badcolumns..$#a){
if ($samplepop{$i}){
$BC{"total"}{"total"}++;
if ($iupac_coding eq "TRUE"){
$a[$i] = $t{$a[$i]};
}
unless (($a[$i] eq "NN")or($a[$i] eq "XX")){
my @bases = split(//, $a[$i]);
$total_alleles{$bases[0]}++;
$total_alleles{$bases[1]}++;
$BC{"total"}{$bases[0]}++;
$BC{"total"}{$bases[1]}++;
$BC{$samplepop{$i}}{$bases[0]}++;
$BC{$samplepop{$i}}{$bases[1]}++;
$BC{"total"}{"Calls"}++;
$BC{$samplepop{$i}}{"Calls"}++;
if($bases[0] ne $bases[1]){
$BC{"total"}{"Het"}++;
$BC{$samplepop{$i}}{"Het"}++;
}
}
}
}
my $pAll;
my $qAll;
my $rAll;
my $HeAll;
my $HoAll;
my $CallRate;
my $p1;
my $q1;
my $r1;
my $p2;
my $q2;
my $r2;
my $Ho1;
my $Ho2;
my $He1 ;
my $He2;
my $Fst;
my $lnRH;
my $private1;
my $private2;
my $privatepresent1;
my $privatepresent2;
my $Fis1;
my $Fis2;
my $shared;
my $dxy;
my $HsBar;
my $fixedDif;
my $H_bar;
my $n_bar;
my $n_1;
my $n_2;
my $n_total;
my $sigma_squared;
my $n_c;
my $WC_a;
my $WC_b;
my $WC_c;
my $WC_denom;
my $WC_fst;
my $pi;
unless ($BC{"total"}{"Calls"}){
$BC{"total"}{"Calls"} = 0;
}
$CallRate = $BC{"total"}{"Calls"}/ $BC{"total"}{"total"};
#print "\t".keys %total_alleles;
if (keys %total_alleles == 2){
#Sort bases so p is the major allele and q is the minor allele
my @bases = sort { $total_alleles{$a} <=> $total_alleles{$b} } keys %total_alleles ;
#Major allele
my $b1 = $bases[1];
#Minor allele
my $b2 = $bases[0];
#Total number of samples
$n_total = $BC{"total"}{"Calls"};
#Major allele frequency in all samples
$pAll = $BC{"total"}{$b1}/($BC{"total"}{"Calls"}*2);
#Minor allele frequency in all samples
$qAll = $BC{"total"}{$b2}/($BC{"total"}{"Calls"}*2);
#Heterozygosity expected in all samples
$HeAll = 2*($pAll * $qAll);
#Heterozygosity observed in all samples
if ($BC{"total"}{"Het"}){
$HoAll = $BC{"total"}{"Het"}/($BC{"total"}{"Calls"}*2);
}else{
$HoAll = 0;
}
#Allele frequency of each allele in each population
if ($BC{$pop1}{$b1}){
$p1 = $BC{$pop1}{$b1}/($BC{$pop1}{"Calls"}*2);
}else{
$p1 = 0;
}
if ($BC{$pop2}{$b1}){
$p2 = $BC{$pop2}{$b1}/($BC{$pop2}{"Calls"}*2);
}else{
$p2 = 0;
}
if ($BC{$pop1}{$b2}){
$q1 = $BC{$pop1}{$b2}/($BC{$pop1}{"Calls"}*2);
}else{
$q1 = 0;
}
if ($BC{$pop2}{$b2}){
$q2 = $BC{$pop2}{$b2}/($BC{$pop2}{"Calls"}*2);
}else{
$q2 = 0;
}
#Heterozygosity observed in each population
if ($BC{$pop1}{"Het"}){
$Ho1 = $BC{$pop1}{"Het"}/$BC{$pop1}{"Calls"}
}else{
$Ho1 = 0;
}
if ($BC{$pop2}{"Het"}){
$Ho2 = $BC{$pop2}{"Het"}/$BC{$pop2}{"Calls"}
}else{
$Ho2 = 0;
}
#Amount of pairwise difference between population
$dxy = (($p1 * $q2) + ($p2 * $q1));
#Heterozygosity expected
$He1 = 2*($p1 * $q1);
$He2 = 2*($p2 * $q2);
my $tmp = 1 / (1 - $He1);
$tmp = $tmp * $tmp;
my $tmpTOP = $tmp -1;
$tmp = 1 / (1 - $He2);
$tmp = $tmp * $tmp;
my $tmpBOT = $tmp -1;
if (($tmpTOP) and ($tmpBOT)){
$lnRH = log( $tmpTOP / $tmpBOT );
}else{
$lnRH = "NA";
}
#print "$tmpTOP\t$tmpBOT\n\n";
#$lnRH = "X";
#Private alleles for each pop
if (($p1 > 0) and ($p2 eq 0)){
$private1 = $b1;
}elsif(($q1 > 0) and ($q2 eq 0)){
$private1 = $b2;
}else{
$private1 = "-";
}
if (($p2 > 0) and ($p1 eq 0)){
$private2 = $b1;
}elsif(($q2 > 0) and ($q1 eq 0)){
$private2 = $b2;
}else{
$private2 = "-";
}
#Presence of private allele?
if ($private1 eq "-"){
$privatepresent1 = 0;
}else{
$privatepresent1 = 1;
}
if ($private2 eq "-"){
$privatepresent2 = 0;
}else{
$privatepresent2 = 1;
}
#Presence of shared polymorphism?
if (($p1 > 0) and ($p2 > 0) and ($q1 > 0) and ($q2 > 0)){
$shared = 1;
}else{
$shared = 0;
}
#Average expected heterozygosity in each population
$HsBar = (($He1+$He2)/2);
#Fst
$Fst = ($HeAll - $HsBar)/ $HeAll;
#Fis for each population
if ($He1 ne 0) {
$Fis1 = ($He1 - $Ho1)/$He1 ;
}else{
$Fis1 = 0;
}
if ($He2 ne 0) {
$Fis2 = ($He2 - $Ho2)/$He2;
}else{
$Fis2 = 0;
}
#Proportion of third alleles in each population and total
$rAll = 0;
$r1 = 0;
$r2 = 0;
#Fixed differences?
if (($p1 == 1) and ($q2 == 1)){
$fixedDif = 1;
}elsif (($p2 == 1) and ($q1 == 1)){
$fixedDif = 1;
}else{
$fixedDif = 0;
}
#Average sample size for populations
$n_bar = ($BC{"total"}{"Calls"} / 2);
#Sample size for population 1
if ($BC{$pop1}{"Calls"}){
$n_1 = $BC{$pop1}{"Calls"};
}else{
$n_1 = 0;
}
#Sample size for population 2
if ($BC{$pop2}{"Calls"}){
$n_2 = $BC{$pop2}{"Calls"};
}else{
$n_2 = 0;
}
#Average observed heterozygosity weighted by population (NEed to scale for sample size)
$H_bar = ((($Ho1 * $n_1) + ($Ho2 * $n_2)) / $n_total);
#Sigma squared. The sample variance of allele p frequencies over populations
$sigma_squared = ((($n_1 * (($p1 - $pAll) ** 2)) / (($Npops - 1) * $n_bar)) + (($n_2 * (($p2 - $pAll) ** 2) / (($Npops - 1) * $n_bar))));
#The squared coefficient of variation of sample sizes
$n_c = ((($Npops * $n_bar) - ((($n_1 ** 2) / ($Npops * $n_bar)) + (($n_2 ** 2) / ($Npops * $n_bar)))) / ($Npops - 1));
#Weir and Cockerham, the observed component of variance for between populations
unless (($n_c eq 0) or ($n_bar <= 1)){
$WC_a = (($n_bar / $n_c) * ($sigma_squared - ((1 / ($n_bar - 1)) * (($pAll * $qAll) - ((($Npops - 1) / $Npops) * $sigma_squared) - (0.25 * $H_bar)))));
}else{
$WC_a = "NA";
}
#Weir and Cockerham, the observed component of variance for between individuals within a population
unless ($n_bar <= 1){
$WC_b = (($n_bar / ($n_bar - 1)) * (($pAll * $qAll) - ((($Npops - 1) / $Npops) * $sigma_squared) - (((2 * $n_bar) - 1) / (4 * $n_bar) * $H_bar)));
}else{
$WC_b = "NA";
}
#Weir and Cockerham, the observed component of variance for between gametes within individuals
$WC_c = (0.5 * $H_bar);
#Weir and Cockerham denominator in Fst calculation
unless (($WC_a eq "NA") or ($WC_b eq "NA")){
$WC_denom = ($WC_a + $WC_b + $WC_c);
}else{
$WC_denom = "NA";
}
#Weir and Cockerham, Theta (Fst)
unless ($WC_denom eq "NA"){
$WC_fst = ($WC_a / $WC_denom);
}else {
$WC_fst = "NA";
}
#Diversity (pi) for single site.
$pi = 2*($pAll * $qAll);
$BiCount++;
}elsif (keys %total_alleles eq 1){
$pAll = 1;
$qAll = 0;
$rAll = 0;
$HeAll = 0;
$HoAll = 0;
$p1 = 1;
$q1 = 0;
$r1 = 0;
$p2 = 1;
$q2 = 0;
$r2 = 0;
$Ho1 = 0;
$Ho2 = 0;
$He1 = 0;
$He2 = 0;
$Fst = "NA";
$lnRH = "NA";
$private1 = "-";
$private2 = "-";
$privatepresent1 = 0;
$privatepresent2 = 0;
$Fis1 = "NA";
$Fis2 = "NA";
$shared = "NA";
$dxy = "NA";
$HsBar = "NA";
$fixedDif = "NA";
$sigma_squared = "NA";
$H_bar = "0";
#Average sample size for populations
$n_bar = ($BC{"total"}{"Calls"} / 2);
#Sample size for population 1
if ($BC{$pop1}{"Calls"}){
$n_1 = $BC{$pop1}{"Calls"};
}else{
$n_1 = 0;
}
if ($BC{$pop2}{"Calls"}){
$n_2 = $BC{$pop2}{"Calls"};
}else{
$n_2 = 0;
}
#Total number of samples
$n_total = $BC{"total"}{"Calls"};
$WC_a = "0";
$WC_b = "0";
$WC_c = "0";
$WC_denom = "0";
$WC_fst = "NA";
$pi = "0";
}
elsif (keys %total_alleles eq 3){ #Need to account for three alleles in tri-allelic sites.
$pAll = "NA";
$qAll = "NA";
$rAll = "NA";
$HeAll = "NA";
$HoAll = "NA";
$p1 = "NA";
$q1 = "NA";
$r1 = "NA";
$p2 = "NA";
$q2 = "NA";
$r2 = "NA";
$Ho1 = "NA";
$Ho2 = "NA";
$He1 = "NA";
$He2 = "NA";
$Fst = "NA";
$lnRH = "NA";
$private1 = "NA";
$private2 = "NA";
$privatepresent1 = "NA";
$privatepresent2 = "NA";
$Fis1 = "NA";
$Fis2 = "NA";
$shared = "NA";
$dxy = "NA"; ##Need to fix
$HsBar = "NA";
$fixedDif = "NA";
$n_total = $BC{"total"}{"Calls"};
$sigma_squared = "NA";
$H_bar = "NA";
$n_1 = "NA";
$n_2 = "NA";
$n_bar = "NA";
$WC_a = "NA"; ##
$WC_b = "NA"; ##
$WC_c = "NA"; ##
$WC_denom = "NA"; ##
$WC_fst = "NA"; ##
$pi = "NA"; ###Need to fix
}elsif ((keys %total_alleles eq 4) or (keys %total_alleles eq 0)){ #If there are four alleles
$pAll = "NA";
$qAll = "NA";
$rAll = "NA";
$HeAll = "NA";
$HoAll = "NA";
$p1 = "NA";
$q1 = "NA";
$r1 = "NA";
$p2 = "NA";
$q2 = "NA";
$r2 = "NA";
$Ho1 = "NA";
$Ho2 = "NA";
$He1 = "NA";
$He2 = "NA";
$Fst = "NA";
$lnRH = "NA";
$private1 = "NA";
$private2 = "NA";
$privatepresent1 = "NA";
$privatepresent2 = "NA";
$Fis1 = "NA";
$Fis2 = "NA";
$shared = "NA";
$dxy = "NA"; ##Need to fix
$HsBar = "NA";
$fixedDif = "NA";
$n_total = $BC{"total"}{"Calls"};
$sigma_squared = "NA";
$H_bar = "NA";
$n_bar = "NA";
$n_1 = "NA";
$n_2 = "NA";
$WC_a = "NA"; ##
$WC_b = "NA"; ##
$WC_c = "NA"; ##
$WC_denom = "NA"; ##
$WC_fst = "NA"; ##
$pi = "NA"; ###Need to fix
}
print "\t$pAll\t$qAll\t$HeAll\t$HoAll\t$CallRate\t$p1\t$q1\t$p2\t$q2\t$Ho1\t$Ho2\t$He1\t$He2\t$Fst\t$lnRH\t$private1\t$private2\t$privatepresent1\t$privatepresent2\t$Fis1\t$Fis2\t$shared\t$dxy\t$HsBar\t$fixedDif\t$n_1\t$n_2\t$H_bar\t$sigma_squared\t$WC_a\t$WC_b\t$WC_c\t$WC_fst\t$pi\n";
}
}
close IN;