# Subset Genepop
#' @title Genepop subset loci and populations
#' @description Function to subset loci and populations
#' @param genepop the genepop data to be manipulated. This can be either a file path
#' or a dataframe read in with tab separation, header=FALSE , quote="", and stringsAsFactors=FALSE.
#' This will be the standard genepop format with the first n+1 rows corresponding to the n loci names,
#' or a single comma delimited row of loci names followed by the locus data. Populations are
#' separated by "Pop". Each individual ID is linked to the locus data by " , " (space,space space) and is read in as
#' as a single row (character).
#' @param subs the loci names of interest or a vector which corresponds to the order of which
#' they appear in the genepop file.
#' These can be either the order by which they occur or the exact name of the loci
#' e.g. subs <-c(1,2,3,4) would return the first 4 loci
#' & subs <- c("190_56","145_21",456_12") would return loci with defined names.
#' @param keep logical vector which defines whether you want to remove the loci or keep them.
#' The default is to keep them keep <- TRUE assuming you are removing neutral markers
#' and only keeping the subs.
#' @param spop is the populations of interest. Note these are specified in the order which they appear in the
#' original genepop file. i.e. first pop = 1 second pop = 2
#' Examples: numeric - spop <- c(1,3,4,7) or
#' the population ID (alpha-numeric code before the underscore). Here we assume conventional
#' naming of "Population_sample#" e.g. (Aqua01_05: population Aqua01 & sample #5).
#' text- spop <- c("Aqua01", "GRR","GHR","TRS").
#' @param path the filepath and filename of output.
#' @rdname subset_genepop
#' @importFrom data.table fread as.data.table
#' @importFrom utils write.table
#' @export
##
subset_genepop <- function(genepop,subs=NULL,keep=TRUE,spop=NULL,path)
{
#Check to see if genepop is a data.frame from the workspace and convert to data.table
if(is.data.frame(genepop)){genepop <- data.table::as.data.table(genepop)}
#Check to see if genepop is a file path or dataframe
if(is.character(genepop)){
genepop <- data.table::fread(genepop,
header = FALSE, sep = "\t",
stringsAsFactors = FALSE)
}
## check if loci names are read in as one large character vector (1 row)
header <- genepop[1,]
if(length(gregexpr(',', header, fixed=F)[[1]])>1){
lociheader <- strsplit(header,",")
lociheader <- gsub(" ","",unlist(lociheader))
#remove the first column of loci names
genepop <- as.vector(genepop)
genepop <- genepop[-1,]
genepop <- c(lociheader,genepop)
genepop <- data.table::as.data.table(genepop,stringsAsFactors = FALSE)
}
## Stacks version information
stacks.version <- genepop[1,] #this could be blank or any other source. First row is ignored by genepop
#Remove first label of the stacks version
genepop <- genepop[-1,]
colnames(genepop) <- "data"
#ID the rows which flag the Populations
Pops <- which(genepop$data == "Pop" | genepop$data =="pop" | genepop$data == "POP")
npops <- 1:length(Pops)
## separate the data into the column headers and the rest
ColumnData <- genepop$data[1:(Pops[1]-1)]
ColumnData <- gsub("\r","",ColumnData)#remove any hidden carriage returns
snpData <- genepop[Pops[1]:NROW(genepop),]
#Get a datafile with just the snp data no pops
tempPops <- which(snpData$data=="Pop"| snpData$data =="pop" | snpData$data == "POP") ## Changed because we allowed
snpData <- snpData[-tempPops,]
#separate the snpdata
temp <- as.data.frame(do.call(rbind, strsplit(snpData$data," ")))
#data format check
if(unique(temp[,2])!="," | !length(which(temp[,3]==""))>1){
stop("Genepop sampleID delimiter not in proper format. Ensure sampleIDs are separated from loci by ' , ' (space comma space space). Function stopped.",call. = FALSE)
}
temp2 <- temp[,4:length(temp)] #split characters by spaces
#Contingency to see if R read in the top line as the "stacks version"
if (length(temp2)!=length(ColumnData)){colnames(temp2) <- c(stacks.version,ColumnData)}
if (length(temp2)==length(ColumnData)){colnames(temp2) <- ColumnData}
if (length(temp2)!=length(ColumnData)){stacks.version="No STACKS version specified"}
#stacks version character
stacks.version <- as.character(stacks.version)
## Get the population names (prior to the _ in the Sample ID)
NamePops <- temp[,1] # Sample names of each
NameExtract <- substr(NamePops,1,regexpr("_",NamePops)-1)
## Now add the population tags using npops (number of populations and Pops for the inter differences)
tPops <- c(Pops,NROW(genepop))
PopIDs <- NULL
for (i in 2:length(tPops)){
hold <- tPops[i]-tPops[i-1]-1
if(i==length(tPops)){hold=hold+1}
pophold <- rep(npops[i-1],hold)
PopIDs <- c(PopIDs,pophold)
}
temp2$Pop <- PopIDs;rm(hold,pophold,tPops,PopIDs)
## Now subset out the the data according to the specified loci and whether or not you want to keep them.
if(is.numeric(subs))
{ #column number instead of name depending on the output from Outlier detection
if(!keep) # neutral
{
if(length(subs)>0){reqCols <- temp2[,-subs]}
if(length(subs)==0){reqCols <- temp2}
}
if(keep) # outliers or loci under divergent selection
{
PopInd=which(names(temp2)=="Pop")
if(length(subs)>0){reqCols <- temp2[,c(subs,PopInd)]}
if(length(subs)==0){reqCols <- temp2}
}
}
if(!is.numeric(subs))
{ #column name
if(!keep)# neutral
{
if(length(subs)>0){reqCols <- temp2[,-which(names(temp2)%in%subs)]}
if(length(subs)==0){reqCols <- temp2}
}
if(keep)# outliers or loci under divergent selection
{
if(length(subs)>0){reqCols <- temp2[,c(subs,"Pop")]}
if(length(subs)==0){reqCols <- temp2}
}
}
## Now subset the rows
# is a population subset required
if(length(spop)>0){
if(sum(is.numeric(spop))>0){ # if the subsetted populations are numeric
ind <- which(reqCols$Pop %in% spop) # index where the populations are
reqCols <- reqCols[ind,]
temp <- temp[ind,]
temp2 <- temp2[ind,]
NamePops <- NamePops[ind]
}
if(sum(is.numeric(spop))==0){ # if the subsetted populations are character indexes
reqCols <- reqCols[which(NameExtract %in% spop),]
temp <- temp[which(NameExtract %in% spop),]
temp2 <- temp2[which(NameExtract %in% spop),]
NamePops <- NamePops[which(NameExtract %in%spop)]
}
} # end of subset population if statement
reqCols <- reqCols[,-length(reqCols)] # delete the "Pop" data * last column
#Now recompile the GenePop format
#the number of individuals for all populations but the last (Pop tagged to the end)
if(length(table(temp2$Pop))>1){PopLengths <- table(temp2$Pop)[-length(table(temp2$Pop))]} else {PopLengths=1}
if(length(table(temp2$Pop))==2){PopPosition = PopLengths+1}
if(length(table(temp2$Pop))>2){
PopPosition <- c(PopLengths[1]+1,rep(NA,(length(PopLengths)-1)))
for (i in 2:length(PopLengths)){
PopPosition[i] <- PopLengths[i]+PopPosition[i-1]
}
}
# paste together the Loci as one long integer separated for each loci by a space
Loci <- do.call(paste,c(reqCols[,], sep=" "))
#Grab the Population tags that each invididual had following the format ID_,__
PopVec <- paste0(NamePops," , ")
#Paste these to the Loci
Loci <- paste(PopVec,Loci,sep="")
#Insert the value of "Pop" which partitions the data among populations #only if more than one population
if(length(table(temp2$Pop))!=1){Loci <- insert_vals(Vec=Loci,breaks=PopPosition,newVal="Pop")}
#Add the first "Pop" label
Loci <- c("Pop",Loci)
## Add the column labels and the stacks version
if(is.numeric(subs))
{ #Column numbers
if(!keep)
{
PopInd=which(names(temp2)=="Pop")
if(length(subs)==0){Output <- c(stacks.version,names(temp2)[-PopInd],Loci)}
if(length(subs)>0){Output <- c(stacks.version,names(temp2)[-c(subs,PopInd)],Loci)}
}
if(keep)
{
PopInd=which(names(temp2)=="Pop")
if(length(subs)==0){Output <- c(stacks.version,names(temp2)[-PopInd],Loci)}
if(length(subs)>0){Output <- c(stacks.version,names(reqCols),Loci)}
}
}
if(!is.numeric(subs))
{ # column names
if(!keep)
{
PopInd=which(names(temp2)=="Pop")
if(length(subs)==0){Output <- c(stacks.version,names(temp2)[-PopInd],Loci)}
if(length(subs)>0){Output <- c(stacks.version,names(temp2)[-which(names(temp2)%in%c(subs,"Pop"))],Loci)}
}
if(keep)
{
PopInd=which(names(temp2)=="Pop")
if(length(subs)==0){Output <- c(stacks.version,names(temp2)[-PopInd],Loci)}
if(length(subs)>0){Output <- c(stacks.version,subs,Loci)}
}
}
# Save the file
utils::write.table(Output,path,col.names=FALSE,row.names=FALSE,quote=FALSE)
} #End function
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