Nothing
#
# ctl.utils.R
#
# copyright (c) 2010-2012 - GBIC, Danny Arends, Bruno Tesson and Ritsert C. Jansen
# last modified Oct, 2012
# first written nov, 2010
#
# check.genotypes, getRVM, lodscorestoscanone, getCorrelatedPhenotypes, gcLoop
check.genotypes <- function(genotypes, geno.enc=c(1,2), minAmount = 20, verbose=FALSE){
if(verbose) cat("check.genotypes: ", ncol(genotypes)," markers, ", nrow(genotypes)," individuals\n")
if(length(geno.enc) < 2) stop("argument 'geno.enc' length is incorrect, provide at least two genotype.values")
toremove <- NULL
idx <- 1
geno.encNaN <- c(geno.enc, NaN, NA)
checks <- apply(genotypes,2 , function(geno){
#We need at least 3 markers of a certain genotype
for(x in geno.enc){
if(length(which(geno==x)) <= minAmount){
if(verbose) cat("Severe: Small/Empty group", x ," (size:",length(which(geno==x)),"), removing marker",idx,"\n")
toremove <<- c(toremove, idx)
}
}
if(any((geno %in% geno.encNaN) == FALSE)){
if(verbose) cat("Severe: Unknown genotype, removing marker",idx,"\n")
toremove <<- c(toremove, idx)
}
idx <<- idx+1
})
toremove <- unique(toremove)
if(length(toremove) > 0){
cat("check.genotypes: Removing", length(toremove),"/",ncol(genotypes), "markers\n")
cat(toremove, "\n")
}
invisible(toremove)
}
#Adds a na.rm = TRUE switch to unique
munique <- function(x, ... , na.rm=TRUE){
res <- unique(x, ...)
if(na.rm && any(is.na(res))) res <- res[-which(is.na(res))]
return(res)
}
#Create a matrix with row length = n.perms, filled with random numbers 1..n.rows
getRVM <- function(n.perms, n.rows){
rvm <- NULL
for(x in 1:n.perms){ rvm <- rbind(rvm,sample(n.rows)); }
rvm
}
#Change any list of lodscores into a scanone object (only pre-req: length(lodscores)==sum(nmar(cross))
lodscorestoscanone <- function(cross,lodscores,traitnames = NULL){
mymap <- qtl::pull.map(cross)
n <- unlist(lapply(FUN=names,mymap))
chr <- NULL
if(!is.null(ncol(mymap[[1]]))){
d <- as.numeric(unlist(lapply(mymap,FUN=function(x) {x[1,]})))
for(i in 1:qtl::nchr(cross)){
chr <- c(chr,rep(names(cross$geno)[i], ncol(mymap[[i]])))
}
}else{
d <- as.numeric(unlist(mymap))
for(i in 1:qtl::nchr(cross)){
chr <- c(chr,rep(names(cross$geno)[i], length(mymap[[i]])))
}
}
qtlprofile <- cbind(chr,d,lodscores)
qtlprofile <- as.data.frame(qtlprofile)
qtlprofile[,1] <- chr
qtlprofile[,2] <- as.numeric(d)
if(!is.null(ncol(lodscores))){
for(x in 1:ncol(lodscores)){
qtlprofile[,2+x] <- as.numeric(lodscores[,x])
}
traitnames = paste("lod",1:ncol(lodscores))
}else{
qtlprofile[,3] <- as.numeric(lodscores)
traitnames = "lod"
}
rownames(qtlprofile) <- n
colnames(qtlprofile) <- c("chr","cM",traitnames)
class(qtlprofile) <- c("scanone", "data.frame")
invisible(qtlprofile)
}
gcLoop <- function(verbose = FALSE){
p_usage <- gc()[2,3]
n_usage <- gc()[2,3]
while(n_usage < p_usage){
p_usage = n_usage
n_usage <- gc()[2,3]
if(verbose) cat("GCloop ",n_usage," ",p_usage,"\n")
}
}
# end of ctl.utils.R
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