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Bootstrapping.per.locus <- function(table2,HWEs){
# Function used within the functions Bootstrapping.p.r and
# Bootstrapping.CI.r to resample alleles/genotypes
if (HWEs[which(names(HWEs)==as.character((table2$locus)[1]))]==TRUE){
# The confidence limits of the measure of genetic distance for the
# several loci and over all loci are determined by a thousandfold
# resampling of the alleles (for each locus
# and all populations) if the populations are in Hardy Weinberg equilibrium.
# Literature: Goudet J, Raymond M, deMeeus T, Rousset F. (1996).
# Testing differentiation in diploid populations. Genetics 144,1933-1940.
allelepool<-as.numeric(as.vector(table2$fragment.length))
# The alleleles that have been found at a locus in all the populations
# are collected in a common vector named 'allelepool'.
resampled.allelepool<-sample(allelepool,length(allelepool),replace=TRUE)
# The alleles from one locus that were found in all populations that
# were sampled, are resampled with replacement.
table2$fragment.length<-resampled.allelepool
# The alleles for the actual locus are replaced with alleles from
# the resampled.allelepool.
table2#tab3<-rbind(tab3,tab2[[l]])
# The tables with the per locus resampled alleles are bound together
# to a single data frame.
}else{
# The confidence limits of the measure of genetic distance for the
# several loci and over all loci are determined by a thousandfold
# resampling of the genotypes (for each locus and all populations)
# if the populations are not in Hardy Weinberg equilibrium.
# Literature: Goudet J, Raymond M, deMeeus T, Rousset F. (1996).
# Testing differentiation in diploid populations. Genetics 144,1933-1940.
table2.genotype <- split(table2$fragment.length,as.vector(table2$individual))
# The genotypes found for the actual locus are filtered out of
# table2. They are now represented according to the frequency
# with which they occured in the empirical data.
number.genotypes <- length(table2.genotype)
# The number of genotypes that have to be resampled.
genotypepool<-as.data.frame(as.matrix(table2.genotype))[1:number.genotypes,]
# The genotypes that have been found for a locus in all the populations
# are collected in a common vector named 'allelepool'.
resampled.genotypepool<-sample(genotypepool,number.genotypes,replace=TRUE)
resampled.genotypepool <- as.numeric(as.vector(unlist(resampled.genotypepool)))
table2$fragment.length <- resampled.genotypepool
# The genotypes for the actual locus are replaced with the genotypes from
# the resampled genotypepool.
table2# tab3<-rbind(tab3,tab2[[l]])
# The tables with the per locus resampled alleles are bound together
# to a single data frame.
}
}
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