https://github.com/jsollari/popABC
Revision e6a0334445b5755bb52a0d2209120ee4e251e7b4 authored by Joao Sollari Lopes on 13 November 2017, 18:32:56 UTC, committed by Joao Sollari Lopes on 13 November 2017, 18:32:56 UTC
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Tip revision: e6a0334445b5755bb52a0d2209120ee4e251e7b4 authored by Joao Sollari Lopes on 13 November 2017, 18:32:56 UTC
First commit
First commit
Tip revision: e6a0334
summstats_sd.c
/*
@author: joao lopes
@workplace: Reading University
@date: 17th October 2008
NBB - based on Mark's translate.c and translateS.c
*/
#include "maketarget.h"
/*
This function calculates the allele number in one population
@param nhap - total number of alleles
@param freq - frequency of an allele
@return the allele number in one population
*/
int calc_nhap(int nhap, int freq[]);
/*
This function calculates the Shannon's index of one population
@param nhap - number of all the haplotypes
@param npop - number of population
@param nsamp - number of samples of a population
@param freq - frequency of haplotypes of a population in a locus
@param cpop - current populations
@result number of haplotypes of one population
*/
double calc_shanon(int nhap, int nsamp, int *freq, int cpop);
/* only used in Microsatellite analysis ********************************************************************/
/*
This function calculates the hetetozygosity in a population
@param sum - size of the sample
@param freq - frequency of a microsatellite size (in number of occurrencies
@param nhap - number of diferent microsatellite sizes
@return the hetetozygosity in one population
*/
double calc_het(int sum,int freq[], int nhap);
/*
This function calculates the variance of allele length in a population
@param sum - size of the sample
@param freq - frequency of a microsatellite size (in number of occurrencies)
@param val - diferent sizes of a microsatellite
@param nhap - number of diferent microsatellite sizes
@return variance of allele length in one population
*/
double calc_var(int sum,int freq[],int val[],int nhap);
/*
This function calculates the curtosis of allele length in a population
@param nhap - total number of microsatellite sizes
@param freq - frequency of a microsatellite size (in number of occurrencies)
@return the allele number in one population
*/
double calc_curt(int nhap, int *freq);
/*
This function calculates the Nm estimator using the heterozygosity
@param Hw - heterozygosity within pop
@param Ha - heterozygosity among pop
@result Nm_H
*/
double calc_Nm_H(double Hw,double Ha);
/* only used in Sequence Data analysis *********************************************************************/
/*
This function is used to caluclate the pairwise difference for one population
@param sum - number of samples
@param freq - frequency of haplotypes of a population in a locus
@param lsites - size of a haplotype in a locus
@param val - all the haplotypes in a locus
@param nhap - number of all the haplotypes
@result pairwise difference of one population
*/
double calc_pi(int sum,int freq[], int lsites, char **val,int nhap);
/*
Number of diferent sites in two diferent haplotypes
@param n - number of sites in the haplotype
@param vi - one haplotype
@param v2 - other haplotype
@result number of diferent sites in the two haplotypes
*/
int numdiff(int n, char *v1, char *v2);
/*
This function is used to caluclate the number of segregate sites of one population
@param sum - number of samples
@param freq - frequency of haplotypes of a population in a locus
@param lsites - size of a haplotype in a locus
@param val - all the haplotypes in a locus
@param nhap - number of all the haplotypes
@param lsnp - SNP in a locus in a population
@result number of segregate sites of one population
*/
double calc_segsites(int sum,int freq[],int lsites, char **val,int nhap, int *lsnp);
/*
This function is used to caluclate the number of segregate sites of populations pooled together
@param sum - number of samples
@param freq - frequency of haplotypes of a population in a locus
@param lsites - size of a haplotype in a locus
@param val - all the haplotypes in a locus
@param nhap - number of all the haplotypes
@result number of segregate sites of one population
*/
double calc_segsites2(int sum,int freq[],int lsites, char **val,int nhap);
/*
This function calculates the Mutation Frequency Spectrum (MFS)
@param val - array with all the haplotypes
@param freq - array with the frequency of all the haplotypes
@param nhap - number of different haplotypes
@param nsites - number of sites of a locus
@param cloc - considered locus
@param cpop - considered population
@param mfs - Mutation Frequency Spectrum
*/
void fillMFS(char **val,int *freq,int nhap,int nsites,int nsamp,int cloc,int cpop,int***mfs);
/*
This function changes a char '1' or '0' to a int 1 or 0
@param c1 - char '1' or '0'
@result int 1 or 0
*/
int segtoint(char c1);
/*
This function calculates the mean of the Mutation Frequency Spectrum (MFS)
@param nsites - number of sites of a locus
@param mfs - MFS
@param snp - number of SNP
@result mean of MFS
*/
double calc_meanMFS(int nsites,int *mfs, int snp);
/*
This function calculates the stdev of the Mutation Frequency Spectrum (MFS)
@param nsites - number of sites of a locus
@param mfs - MFS
@param snp - number of SNP
@param lsnp - list the SNPs
@param mMFS - mean of MFS
@result stdev of MFS
*/
double calc_stdevMFS(int nsites,int *mfs, int snp, int *lsnp, double mMFS);
/*
This function calculates the Nm estimator using the segregating sites
@param Sw - no segregating sites within pop
@param Sa - no segregating sites among pop
@result Nm_S
*/
double calc_Nm_S(double Sw,double Sa);
/*
This function calculates the number of private segregating sites
@param nsites - number of sites of the current locus
@param npop - total number of populations
@param pop - current population
@param loc - current locus
@param lsnp - SNP per site per loci per pop
@result privateS
*/
double calc_privS(int nsites, int npop, int pop, int loc,int*** lsnp);
/*
This function calculates the average frequency of private segregating sites
@param nsites - number of sites of the current locus
@param npop - total number of populations
@param nhap -
@param pop - current population
@param loc - current locus
@param lsnp - SNP per locus per pop per site
@param freq - array with the frequency of all the haplotypes
@param val - array with all the haplotypes
@result S_1
*/
double calc_S_1(int nsites, int npop, int nhap, int pop,int loc,int ***lsnp,int **freq,char **val);
void summStats(struct data *data,int *lsstats,char *outp,int foundSTR,int foundSNP,char *ltype){
int cloc,cdna,cpop,cpop2,csite,ic, //iterators
maxDna, //maximum number of different haplotypes of all loci
npop, //number of population
nloc, //number of loci
tpop, //iterator for two populations
tsamp, //size of sample of two populations
skip, //number of loci with 1 or less samples
npair, //number of population pairs
*tfreq, //sum of the frequencies of diferent microsatellites size of two populations
*ldna, //number of diferent alleles sizes by loci
**nsamp, //size of sample per locus per population
***freq; //all the frequencies of the diferent microsatellite sizes by pop and loci
/*only used in microssatellites data*/
int **valM; //all the diferent microsatellite sizes by loci
double sstats1_t, //heterozygosity for all populations pooled together
*sstats1, //heterozygosity difference in each population
*sstats2, //variance of allele length in each population
*sstats3, //allele no. in each population
*sstats4, //curtosis of allele lengths in each population
*sstats5, //Shanon's index in each population
*sstats6, //Nm_H in each population
*sstats1_2, //heterozygosity for each pair of population pooled together
*sstats2_2, //variance of allele length for each pair of population pooled together
*sstats3_2, //allele no.for each pair of population pooled togther
*sstats4_2, //curtosis of allele lengths for each pair of population pooled together
*sstats5_2; //Shanon's index for each pair of population pooled togther
/*only used in sequence data*/
int *lsites, //size of the haplotypes by loci
***mfs, //mutation frequency spectrum (MFS) by loci by pop
**snp, //number of SNPs by loci by pop
***lsnp; //SNP per sites per loci per pop
double sstats8_t, //segregate sites no. for all populations pooled together
*sstats7, //pairwise difference in each population
*sstats8, //segregate sites no. in each population
*sstats9, //haplotypes no. in each population
*sstats10, //Shanon's index in each population
*sstats11, //mean of mutation frequency spectrum (MFS) in each population
*sstats12, //stdev of mutation frequency spectrum (MFS) in each population
*sstats13, //Nm_S in each population
*sstats14, //private S in each population
*sstats15, //S(1) in each population
*sstats7_2, //pairwise difference for each pair of population pooled together
*sstats8_2, //segregate sites no. for each pair of population pooled together
*sstats9_2, //haplotypes no. for each pair of population pooled togther
*sstats10_2, //Shanon's index for each pair of population pooled togther
**mMFS; //mean of MFS by loci by pop
char ***valS; //all the diferent haplotypes by loci
npop = data->npop;
nloc = data->nloc;
ldna = data->ldna;
nsamp = data->nsamp;
freq = data->freq;
npair = combinations(npop,2);
if(foundSTR)
valM = data->valM;
if(foundSNP){
valS = data->valS;
lsites = data->lsites;
}
/*allocate memory*/
maxDna = ldna[0];
for(cloc=1 ; cloc<nloc ; cloc++){
if(maxDna<ldna[cloc])
maxDna = ldna[cloc];
}
tfreq = (int *)malloc(maxDna*sizeof(int));
if(foundSTR){
sstats1 = (double *)malloc(npop*sizeof(double));
sstats2 = (double *)malloc(npop*sizeof(double));
sstats3 = (double *)malloc(npop*sizeof(double));
sstats4 = (double *)malloc(npop*sizeof(double));
sstats5 = (double *)malloc(npop*sizeof(double));
sstats6 = (double *)malloc(npop*sizeof(double));
sstats1_2 = (double *)malloc(npair*sizeof(double));
sstats2_2 = (double *)malloc(npair*sizeof(double));
sstats3_2 = (double *)malloc(npair*sizeof(double));
sstats4_2 = (double *)malloc(npair*sizeof(double));
sstats5_2 = (double *)malloc(npair*sizeof(double));
}
if(foundSNP){
snp = (int **)malloc(npop*sizeof(int*));
lsnp = (int ***)malloc(npop*sizeof(int**));
mfs = (int ***)malloc(npop*sizeof(int**));
mMFS = (double **)malloc(npop*sizeof(double*));
for(cpop=0; cpop<npop; cpop++){
snp[cpop] = (int *)malloc(nloc*sizeof(int));
lsnp[cpop] = (int **)malloc(nloc*sizeof(int*));
mMFS[cpop] = (double *)malloc(nloc*sizeof(double));
mfs[cpop] = (int **)malloc(nloc*sizeof(int*));
for(cloc=0; cloc<nloc; cloc++){
mfs[cpop][cloc] = (int *)malloc(lsites[cloc]*sizeof(int));
lsnp[cpop][cloc] = (int *)malloc(lsites[cloc]*sizeof(int));
}
}
sstats7 = (double *)malloc(npop*sizeof(double));
sstats8 = (double *)malloc(npop*sizeof(double));
sstats9 = (double *)malloc(npop*sizeof(double));
sstats10 = (double *)malloc(npop*sizeof(double));
sstats11 = (double *)malloc(npop*sizeof(double));
sstats12 = (double *)malloc(npop*sizeof(double));
sstats13 = (double *)malloc(npop*sizeof(double));
sstats14 = (double *)malloc(npop*sizeof(double));
sstats15 = (double *)malloc(npop*sizeof(double));
sstats7_2 = (double *)malloc(npair*sizeof(double));
sstats8_2 = (double *)malloc(npair*sizeof(double));
sstats9_2 = (double *)malloc(npair*sizeof(double));
sstats10_2 = (double *)malloc(npair*sizeof(double));
}
/*start calculating the summary statistics*/
memset(outp,'\0',sizeof(outp));
if(foundSTR){
/*hetetozygosity in each population */
if(lsstats[0]==1){
for(cpop = 0;cpop <npop;++cpop){
sstats1[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] <= 1 || ltype[cloc] == 'S' || ltype[cloc] == 's'){
++skip;
continue;
}
sstats1[cpop] += calc_het(nsamp[cloc][cpop],freq[cloc][cpop],ldna[cloc]);
}
if(nloc-skip==0)
sstats1[cpop]=0;
else
sstats1[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats1[cpop]);
}
}
/*variance of allele length in each population */
if(lsstats[1]==1){
for(cpop = 0;cpop <npop;++cpop){
sstats2[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] <= 1 || ltype[cloc] == 'S' || ltype[cloc] == 's'){
++skip;
continue;
}
sstats2[cpop] += calc_var(nsamp[cloc][cpop],freq[cloc][cpop],valM[cloc],ldna[cloc]);
}
if(nloc-skip==0)
sstats2[cpop]=0;
else
sstats2[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats2[cpop]);
}
}
/*allele number in each population */
if(lsstats[2]==1){
for(cpop = 0;cpop <npop;++cpop){
sstats3[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] < 1 || ltype[cloc] == 'S' || ltype[cloc] == 's'){
++skip;
continue;
}
sstats3[cpop] += calc_nhap(ldna[cloc],freq[cloc][cpop]);
}
if(nloc-skip==0)
sstats3[cpop]=0;
else
sstats3[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats3[cpop]);
}
}
/*curtosis of allele length in each population */
if(lsstats[3]==1){
for(cpop = 0;cpop <npop;++cpop){
sstats4[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] <= 1 || ltype[cloc] == 'S' || ltype[cloc] == 's'){
++skip;
continue;
}
sstats4[cpop] += calc_curt(ldna[cloc],freq[cloc][cpop]);
}
if(nloc-skip==0)
sstats4[cpop]=0;
else
sstats4[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats4[cpop]);
}
}
/*Shanon's index for each population */
if(lsstats[4]==1){
for(cpop=0 ; cpop<npop ; ++cpop){
sstats5[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] < 1 || ltype[cloc] == 'S' || ltype[cloc] == 's'){
++skip;
continue;
}
sstats5[cpop] += calc_shanon(ldna[cloc],nsamp[cloc][cpop],freq[cloc][cpop],cpop);
}
if(nloc-skip==0)
sstats5[cpop]=0;
else
sstats5[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats5[cpop]);
}
}
/*heterozygosity for all populations pooled together */
if(lsstats[5]==1 && npop>1){
tsamp=0;
for(cdna=0;cdna<maxDna;++cdna)
tfreq[cdna]=0;
for(cpop = 0;cpop <npop;++cpop) {
for(cloc=0;cloc<nloc;++cloc){
tsamp += nsamp[cloc][cpop];
for(cdna=0;cdna<ldna[cloc];++cdna)
tfreq[cdna] += freq[cloc][cpop][cdna];
}
}
sstats1_t = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(tsamp <= 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
++skip;
continue;
}
sstats1_t += calc_het(tsamp,tfreq,ldna[cloc]);
}
if(nloc-skip==0)
sstats1_t=0;
else
sstats1_t /= nloc-skip;
}
/*Nm_H in each population */
if(lsstats[5]==1 && npop>1){
for(cpop = 0;cpop <npop;++cpop){
sstats6[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] <= 1 || ltype[cloc] == 'S' || ltype[cloc] == 's'){
++skip;
continue;
}
sstats6[cpop] += calc_Nm_H(sstats1[cpop],sstats1_t);
}
if(nloc-skip==0)
sstats6[cpop]=0;
else
sstats6[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats6[cpop]);
}
}
/*heterozygosity for each pair of population pooled together */
if(lsstats[0]==1){
for(cpop = 0,ic=0;cpop <npop;++cpop){
for(cpop2 = cpop+1;cpop2 < npop;++cpop2){
sstats1_2[ic] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] + nsamp[cloc][cpop2] <= 1 || ltype[cloc] == 'S' || ltype[cloc] == 's') {
++skip;
continue;
}
tsamp = nsamp[cloc][cpop]+nsamp[cloc][cpop2];
for(cdna=0;cdna<ldna[cloc];++cdna)
tfreq[cdna] = freq[cloc][cpop][cdna] + freq[cloc][cpop2][cdna];
sstats1_2[ic] += calc_het(tsamp,tfreq,ldna[cloc]);
}
if(nloc-skip==0)
sstats1_2[ic]=0;
else
sstats1_2[ic] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats1_2[ic]);
++ic;
}
}
}
/*variance of allele lengths for each pair of population pooled together */
if(lsstats[1]==1){
for(cpop = 0,ic=0;cpop <npop;++cpop){
for(cpop2 = cpop+1;cpop2 < npop;++cpop2){
sstats2_2[ic] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] + nsamp[cloc][cpop2] <= 1 || ltype[cloc] == 'S' || ltype[cloc] == 's'){
++skip;
continue;
}
tsamp = nsamp[cloc][cpop]+nsamp[cloc][cpop2];
for(cdna=0;cdna<ldna[cloc];++cdna)
tfreq[cdna] = freq[cloc][cpop][cdna] + freq[cloc][cpop2][cdna];
sstats2_2[ic] += calc_var(tsamp,tfreq,valM[cloc],ldna[cloc]);
}
if(nloc-skip==0)
sstats2_2[ic]=0;
else
sstats2_2[ic] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats2_2[ic]);
++ic;
}
}
}
/*number of alleles for each pair of population pooled together */
if(lsstats[2]==1){
for(cpop = 0,ic=0;cpop <npop;++cpop){
for(cpop2 = cpop+1;cpop2 < npop;++cpop2){
sstats3_2[ic] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] + nsamp[cloc][cpop2] < 1 || ltype[cloc] == 'S' || ltype[cloc] == 's'){
++skip;
continue;
}
for(cdna=0;cdna<ldna[cloc];++cdna)
tfreq[cdna] = freq[cloc][cpop][cdna] + freq[cloc][cpop2][cdna];
sstats3_2[ic] += calc_nhap(ldna[cloc],tfreq);
}
if(nloc-skip==0)
sstats3_2[ic]=0;
else
sstats3_2[ic] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats3_2[ic]);
++ic;
}
}
}
/*curtosis of allele lengths for each pair of population pooled together */
if(lsstats[3]==1){
for(cpop = 0,ic=0;cpop <npop;++cpop){
for(cpop2 = cpop+1;cpop2 < npop;++cpop2){
sstats4_2[ic] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] + nsamp[cloc][cpop2] <= 1 || ltype[cloc] == 'S' || ltype[cloc] == 's'){
++skip;
continue;
}
for(cdna=0;cdna<ldna[cloc];++cdna)
tfreq[cdna] = freq[cloc][cpop][cdna] + freq[cloc][cpop2][cdna];
sstats4_2[ic] += calc_curt(ldna[cloc],tfreq);
}
if(nloc-skip==0)
sstats4_2[ic]=0;
else
sstats4_2[ic] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats4_2[ic]);
++ic;
}
}
}
/*Shanon's index for each pair of populations pooled together */
if(lsstats[4]==1){
for(cpop = 0,ic=0;cpop <npop;++cpop){
for(cpop2 = cpop+1;cpop2 < npop;++cpop2){
sstats5_2[ic] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] + nsamp[cloc][cpop2] < 1 || ltype[cloc] == 'S' || ltype[cloc] == 's'){
++skip;
continue;
}
tsamp = nsamp[cloc][cpop]+nsamp[cloc][cpop2];
for(cdna=0;cdna<ldna[cloc];++cdna)
tfreq[cdna] = freq[cloc][cpop][cdna] + freq[cloc][cpop2][cdna];
sstats5_2[ic] += calc_shanon(ldna[cloc],tsamp,tfreq,cpop);
}
if(nloc-skip==0)
sstats5_2[ic]=0;
else
sstats5_2[ic] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats5_2[ic]);
++ic;
}
}
}
}
if(foundSNP){
/*pairwise difference for each population */
if(lsstats[6]==1){
for(cpop = 0;cpop <npop;++cpop){
sstats7[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] <= 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
++skip;
continue;
}
sstats7[cpop] += calc_pi(nsamp[cloc][cpop],freq[cloc][cpop],lsites[cloc],valS[cloc],ldna[cloc]);
}
if(nloc-skip==0)
sstats7[cpop]=0;
else
sstats7[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats7[cpop]);
}
}
//fill lsnp
if(lsstats[7]==1){
for(cpop=0; cpop<npop; cpop++){
for(cloc=0; cloc<nloc; cloc++){
for(csite=0;csite<lsites[cloc];csite++)
lsnp[cpop][cloc][csite]=0;
}
}
}
/*number of segregating sites for each population */
if(lsstats[7]==1){
for(cpop = 0;cpop <npop;++cpop){
sstats8[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] <= 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
++skip;
continue;
}
snp[cpop][cloc]=calc_segsites(nsamp[cloc][cpop],freq[cloc][cpop],lsites[cloc],
valS[cloc],ldna[cloc],lsnp[cpop][cloc]);
sstats8[cpop]+=snp[cpop][cloc];
}
if(nloc-skip==0)
sstats8[cpop]=0;
else
sstats8[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats8[cpop]);
}
}
/*number of haplotypes for each population */
if(lsstats[8]==1){
for(cpop = 0;cpop <npop;++cpop) {
sstats9[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc)
{
if(nsamp[cloc][cpop] < 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
++skip;
continue;
}
sstats9[cpop] += calc_nhap(ldna[cloc],freq[cloc][cpop]);
}
if(nloc-skip==0)
sstats9[cpop]=0;
else
sstats9[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats9[cpop]);
}
}
/*Shanon's index for each population */
if(lsstats[9]==1){
for(cpop=0 ; cpop<npop ; ++cpop){
sstats10[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] < 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
++skip;
continue;
}
sstats10[cpop] += calc_shanon(ldna[cloc],nsamp[cloc][cpop],freq[cloc][cpop],cpop);
}
if(nloc-skip==0)
sstats10[cpop]=0;
else
sstats10[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats10[cpop]);
}
}
/*build a mutation frequency spectrum (MFS)*/
if(lsstats[10]==1 || lsstats[11]==1){
for(cpop = 0;cpop <npop;++cpop) {
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] < 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
continue;
}
fillMFS(valS[cloc],freq[cloc][cpop],ldna[cloc],lsites[cloc],nsamp[cloc][cpop],cloc,cpop,mfs);
}
}
}
/*mean of mutation frequency spectrum (MFS) in each population*/
if(lsstats[10]==1){
for(cpop = 0;cpop <npop;++cpop) {
sstats11[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] < 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
++skip;
continue;
}
mMFS[cpop][cloc]=calc_meanMFS(lsites[cloc],mfs[cpop][cloc],snp[cpop][cloc]);
sstats11[cpop]+=mMFS[cpop][cloc];
}
if(nloc-skip==0)
sstats11[cpop]=0;
else
sstats11[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats11[cpop]);
}
}
/*stdev of mutation frequency spectrum (MFS) in each population*/
if(lsstats[11]==1){
for(cpop = 0;cpop <npop;++cpop){
sstats12[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] < 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
++skip;
continue;
}
sstats12[cpop]+= calc_stdevMFS(lsites[cloc],mfs[cpop][cloc],snp[cpop][cloc],lsnp[cpop][cloc],mMFS[cpop][cloc]);
}
if(nloc-skip==0)
sstats12[cpop]=0;
else
sstats12[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats12[cpop]);
}
}
/*number of segregate sites for all the populations pooled together */
if(lsstats[12]==1 && npop>1){
tsamp=0;
for(cdna=0;cdna<maxDna;++cdna)
tfreq[cdna]=0;
for(cpop = 0;cpop <npop;++cpop){
for(cloc=0;cloc<nloc;++cloc){
tsamp += nsamp[cloc][cpop];
for(cdna=0;cdna<ldna[cloc];++cdna)
tfreq[cdna] += freq[cloc][cpop][cdna];
}
}
sstats8_t = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc)
{
if(tsamp <= 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm')
{
++skip;
continue;
}
sstats8_t += calc_segsites2(tsamp,tfreq,lsites[cloc],valS[cloc],ldna[cloc]);
}
if(nloc-skip==0)
sstats8_t=0;
else
sstats8_t /= nloc-skip;
}
/*Nm_S in each population */
if(lsstats[12]==1 && npop>1){
for(cpop = 0;cpop <npop;++cpop){
sstats13[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] <= 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
++skip;
continue;
}
sstats13[cpop] += calc_Nm_S(sstats8[cpop],sstats8_t);
}
if(nloc-skip==0)
sstats13[cpop]=0;
else
sstats13[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats13[cpop]);
}
}
/*private S in each population */
if(lsstats[13]==1 && npop>1){
for(cpop = 0;cpop <npop;++cpop){
sstats14[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] <= 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
++skip;
continue;
}
sstats14[cpop]+=calc_privS(lsites[cloc],npop,cpop,cloc,lsnp);
}
if(nloc-skip==0)
sstats14[cpop]=0;
else
sstats14[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats14[cpop]);
}
}
/*S(1) in each population */
if(lsstats[14]==1 && npop>1){
for(cpop = 0;cpop <npop;++cpop){
sstats15[cpop] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] <= 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
++skip;
continue;
}
sstats15[cpop] += calc_S_1(lsites[cloc],npop,ldna[cloc],cpop,cloc,lsnp,freq[cloc],valS[cloc]);
}
if(nloc-skip==0)
sstats15[cpop]=0;
else
sstats15[cpop] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats15[cpop]);
}
}
/*pairwise difference for each pair of populations pooled together */
if(lsstats[6]==1){
for(cpop = 0,ic=0;cpop <npop;++cpop){
for(cpop2 = cpop+1;cpop2 < npop;++cpop2){
sstats7_2[ic] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] + nsamp[cloc][cpop2] <= 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
++skip;
continue;
}
tsamp = nsamp[cloc][cpop]+nsamp[cloc][cpop2];
for(cdna=0;cdna<ldna[cloc];++cdna)
tfreq[cdna] = freq[cloc][cpop][cdna] + freq[cloc][cpop2][cdna];
sstats7_2[ic] += calc_pi(tsamp,tfreq,lsites[cloc],valS[cloc],ldna[cloc]);
}
if(nloc-skip==0)
sstats7_2[ic]=0;
else
sstats7_2[ic] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats7_2[ic]);
++ic;
}
}
}
/*number of segregate sites for each pair of populations pooled together */
if(lsstats[7]==1){
for(cpop = 0,ic=0;cpop <npop;++cpop){
for(cpop2 = cpop+1;cpop2 < npop;++cpop2){
sstats8_2[ic] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] + nsamp[cloc][cpop2] <= 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
++skip;
continue;
}
tsamp = nsamp[cloc][cpop]+nsamp[cloc][cpop2];
for(cdna=0;cdna<ldna[cloc];++cdna)
tfreq[cdna] = freq[cloc][cpop][cdna] + freq[cloc][cpop2][cdna];
sstats8_2[ic] += calc_segsites2(tsamp,tfreq,lsites[cloc],valS[cloc],ldna[cloc]);
}
if(nloc-skip==0)
sstats8_2[ic]=0;
else
sstats8_2[ic] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats8_2[ic]);
++ic;
}
}
}
/*number of haplotypes for each pair of populations pooled together */
if(lsstats[8]==1){
for(cpop = 0,ic=0;cpop <npop;++cpop){
for(cpop2 = cpop+1;cpop2 < npop;++cpop2){
sstats9_2[ic] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] + nsamp[cloc][cpop2] < 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
++skip;
continue;
}
for(cdna=0;cdna<ldna[cloc];++cdna)
tfreq[cdna] = freq[cloc][cpop][cdna] + freq[cloc][cpop2][cdna];
sstats9_2[ic] += calc_nhap(ldna[cloc],tfreq);
}
if(nloc-skip==0)
sstats9_2[ic]=0;
else
sstats9_2[ic] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats9_2[ic]);
++ic;
}
}
}
/*Shanon's index for each pair of populations pooled together */
if(lsstats[9]==1){
for(cpop = 0,ic=0;cpop <npop;++cpop){
for(cpop2 = cpop+1;cpop2 < npop;++cpop2){
sstats10_2[ic] = 0;
skip = 0;
for(cloc=0;cloc<nloc;++cloc){
if(nsamp[cloc][cpop] + nsamp[cloc][cpop2] < 1 || ltype[cloc] == 'M' || ltype[cloc] == 'm'){
++skip;
continue;
}
tsamp = nsamp[cloc][cpop]+nsamp[cloc][cpop2];
for(cdna=0;cdna<ldna[cloc];++cdna)
tfreq[cdna] = freq[cloc][cpop][cdna] + freq[cloc][cpop2][cdna];
sstats10_2[ic] += calc_shanon(ldna[cloc],tsamp,tfreq,cpop);
}
if(nloc-skip==0)
sstats10_2[ic]=0;
else
sstats10_2[ic] /= nloc-skip;
sprintf(outp+strlen(outp),"%g ",sstats10_2[ic]);
++ic;
}
}
}
}
//write informations to string outp
sprintf(outp+strlen(outp),"\n");
/*free stuff*/
free(tfreq);
if(foundSTR){
free(sstats1);
free(sstats2);
free(sstats3);
free(sstats4);
free(sstats5);
free(sstats6);
free(sstats1_2);
free(sstats2_2);
free(sstats3_2);
free(sstats4_2);
free(sstats5_2);
}
if(foundSNP){
for(cpop=0; cpop<npop; cpop++){
for(cloc=0; cloc<nloc; cloc++){
free(mfs[cpop][cloc]);
free(lsnp[cpop][cloc]);
}
free(snp[cpop]);
free(lsnp[cpop]);
free(mMFS[cpop]);
free(mfs[cpop]);
}
free(snp);
free(lsnp);
free(mMFS);
free(mfs);
free(sstats7);
free(sstats8);
free(sstats9);
free(sstats10);
free(sstats11);
free(sstats12);
free(sstats13);
free(sstats14);
free(sstats15);
free(sstats7_2);
free(sstats8_2);
free(sstats9_2);
free(sstats10_2);
}
} //end of get_summstats
int calc_nhap(int nhap, int freq[]){
int chap, //iterator
ndna;
ndna = 0;
for(chap=0;chap<nhap;chap++)
if(freq[chap] > 0)
++ndna;
return ndna;
} //end of calc_nhap
double calc_shanon(int nhap, int nsamp, int *freq, int cpop){
int chap; //iterators
double shan,
p;
shan = 0.0;
for(chap=0;chap<nhap;++chap){
if(freq[chap]!=0&&nsamp!=0){
p = freq[chap]/(double)nsamp;
shan -= p*(log(p)/log(2.0));
}
}
return(shan);
} //end of calc_shanon
double calc_var(int sum,int freq[],int val[],int nhap){
int chap; //iterator
double x,
x2;
x = 0;
for(chap=0;chap<nhap;++chap){
x += val[chap]*freq[chap];
}
x /= sum;
x2 = 0;
for(chap=0;chap<nhap;++chap){
x2 += (val[chap]-x)*(val[chap]-x)*freq[chap];
}
x2 /= sum-1;
return(x2);
} //end of calc_var
double calc_curt(int nhap, int *freq){
int chap; //iterator
double curt,
*x1,
*x2,
*x3,
*x4,
*min,
*max,
*dfreq;
dfreq=(double*)malloc(nhap*sizeof(double));
x1=(double*)malloc(nhap*sizeof(double));
x2=(double*)malloc(nhap*sizeof(double));
x3=(double*)malloc(nhap*sizeof(double));
x4=(double*)malloc(nhap*sizeof(double));
min=(double*)malloc(nhap*sizeof(double));
max=(double*)malloc(nhap*sizeof(double));
for(chap=0 ; chap<nhap ; chap++)
dfreq[chap]=freq[chap];
curt=0.0;
mom(dfreq,nhap,x1,x2,x3,x4,min,max);
curt=*x4;
free(dfreq);
free(x1);
free(x2);
free(x3);
free(x4);
free(min);
free(max);
return curt;
} //end of calc_curt
double calc_het(int sum,int freq[], int nhap){
int chap; //iterator
double het;
het = 0;
for(chap=0;chap<nhap;++chap){
het += freq[chap]*freq[chap];
}
het = sum/(sum-1.0)*(1-het/(sum*sum));
return(het);
} //end of calc_het
double calc_Nm_H(double Hw,double Ha){
if(Ha-Hw<=0)
return Hw;
else
return Hw/(1 + Ha - Hw);
} //end of calc_Nm_H
double calc_pi(int sum,int freq[], int nsites, char **val,int nhap){
int chap,chap2; //iterators
double het;
het = 0;
for(chap=0;chap<nhap;++chap){
for(chap2=chap+1;chap2<nhap;++chap2){
het += freq[chap]*freq[chap2]*numdiff(nsites,val[chap],val[chap2]);
}
}
het /= sum*(sum-1)/2;
return(het);
} //end of calc_pi
int numdiff(int nsites, char *hap1, char *hap2){
int csite,
sum;
sum = 0;
for(csite=0;csite<nsites;++csite)
if(hap1[csite] != hap2[csite])
++sum;
return sum;
} //end of numdiff
double calc_segsites(int sum,int freq[],int nsites, char **val,int nhap,int *lsnp){
int csite,chap, //iterators
ip;
double nS;
nS = 0;
/* find first haplotype that has freq > 0 in this pop */
for(chap=0;chap<nhap;++chap)
if(freq[chap] > 0)
break;
ip = chap;
for(csite=0;csite<nsites;++csite){
for(chap=1;chap<nhap;++chap){
if(freq[chap] == 0)continue; /* ignore haplotype with 0 freq */
if(val[chap][csite] != val[ip][csite]){
nS++;
lsnp[csite]=1;
break;
}
}
}
return nS;
} //end of calc_segsites
double calc_segsites2(int sum,int freq[],int nsites, char **val,int nhap){
int csite,chap, //iterators
ip;
double x;
x = 0;
/* find first haplotype that has freq > 0 in this pop */
for(chap=0;chap<nhap;++chap)
if(freq[chap] > 0)
break;
ip = chap;
for(csite=0;csite<nsites;++csite){
for(chap=1;chap<nhap;++chap){
if(freq[chap] == 0)continue; /* ignore haplotype with 0 freq */
if(val[chap][csite] != val[ip][csite]){
++x;
break;
}
}
}
return x;
} //end of calc_segsites
void fillMFS(char **val,int *freq,int nhap,int nsites,int nsamp,int cloc,int cpop,int ***mfs){
int chap,csite, //iterators
aux;
//fill mfs[][][]
for(csite=0; csite<nsites; csite++){
aux=0;
for(chap=0; chap<nhap; chap++){
aux+=freq[chap]*segtoint(val[chap][csite]);
}
if(aux>nsamp/2)
aux=nsamp-aux;
mfs[cpop][cloc][csite]=aux;
}
} //end of fillMFS
int segtoint(char c1){
if(c1=='0')
return 0;
else
return 1;
} //end of segtoint
double calc_meanMFS(int nsites,int *mfs,int snp){
int csite; //iterators
double aver; //average of MFS
aver=0;
for(csite=0; csite<nsites; csite++){
aver+=mfs[csite];
}
if(snp>0)
return aver/(double)snp;
else
return 0;
} //end of calc_meanMFS
double calc_stdevMFS(int nsites,int *mfs,int snp,int *lsnp,double mMFS){
int csite; //iterators
double stdev; //stdev of MFS
if(snp>1){
stdev = 0;
for(csite=0; csite<nsites; csite++){
if(lsnp[csite])
stdev += pow(mfs[csite]-mMFS,2);
}
stdev = stdev/((double)snp-1);
return pow(stdev,0.5);
}
else
return 0;
} //end of calc_stdevMFS
double calc_Nm_S(double Sw,double Sa){
if(Sa-Sw<=0)
return Sw;
else
return Sw/(Sa - Sw);
} //end of calc_Nm_S
double calc_privS(int nsites, int npop, int pop, int loc,int ***lsnp){
int cpop,csite, //iterators
priv,
nS;
nS = 0;
for(csite=0;csite<nsites;++csite){
if(lsnp[pop][loc][csite]==1){
priv = 1;
for(cpop=0; cpop<npop; cpop++){
if(cpop==pop)
continue;
if(lsnp[cpop][loc][csite]==1){
priv=0;
break;
}
}
if(priv){
++nS;
}
}
}
return nS;
} //end of calc_privS
double calc_S_1(int nsites, int npop, int nhap, int pop, int loc, int ***lsnp, int **freq,char **val){
int cpop,chap,csite, //iterators
gotS,
priv,
nS;
double S_1;
char otherS;
nS = 0;
S_1 = 0.0;
for(csite=0;csite<nsites;++csite){
if(lsnp[pop][loc][csite]==1){
gotS = 0;
priv = 1;
for(cpop=0; cpop<npop; cpop++){
if(cpop==pop)
continue;
if(lsnp[cpop][loc][csite]==1){
priv=0;
break;
}
else{
for(chap=0; chap<nhap && !gotS; chap++){
if(freq[cpop][chap] == 0)continue; /* ignore haplotype with 0 freq */
otherS = val[chap][csite];
gotS = 1;
}
}
}
if(priv){
for(chap=0; chap<nhap; chap++){
if(freq[pop][chap] == 0)continue; /* ignore haplotype with 0 freq */
if(val[chap][csite]!=otherS)
S_1 +=freq[pop][chap];
}
++nS;
}
}
}
if(nS == 0)
S_1 = 0;
else
S_1 /= nS;
return S_1;
} //end of calc_S_1
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