Nothing
#' @title Writes a bayescan file
#'
#' @description write the genotypes in a format suitable for
#' analysis with bayescan
#'
#' @usage write.bayescan(dat=dat,diploid=TRUE,fn="dat.bsc")
#'
#' @param dat a genotype data frame
#' @param diploid whether the dataset is diploid or haploid
#' @param fn file name for output
#'
#' @return a text file fn is written in the current directory
#'
#' @author Jerome Goudet \email{jerome.goudet@@unil.ch}
#'
#' @references \href{https://academic.oup.com/genetics/article/180/2/977/6073889}{Foll M and OE Gaggiotti (2008)
#' Genetics 180: 977-993}
#'
#'
#' \url{http://cmpg.unibe.ch/software/BayeScan/}
#'
#'@export
#'
#'
##############################################
write.bayescan<-function(dat=dat,diploid=TRUE,fn="dat.bsc"){
nloc<-dim(dat)[2]-1
npop<-length(table(dat[,1]))
alc.dat<-allele.count(dat,diploid)
nal<-unlist(lapply(alc.dat,function(x) dim(x)[1]))
nindx<-sapply(alc.dat,function(x) apply(x,2,sum))
write(paste("[loci]=",nloc,sep=""),fn)
write("",fn,append=TRUE)
write(paste("[populations]=",npop,sep=""),fn,append=TRUE)
write("",fn,append=TRUE)
for (ip in 1:npop){
write("",fn,append=TRUE)
write(paste("[pop]=",ip,sep=""),fn,append=TRUE)
for (il in 1:nloc){
tow<-c(il,nindx[ip,il],nal[il],alc.dat[[il]][,ip])
write(tow,fn,
append=TRUE,ncolumns=length(tow))
}
}
}
Any scripts or data that you put into this service are public.
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.