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#' @title Calculation of fractional copy numbers for the CNVs and CNV regions.
#'
#' @description This generic function calculates the fractional copy numbers of
#' a CNV detection method stored in an instance of
#' \code{\link{CNVDetectionResult-class}}. Must be a result of
#' "referencecn.mops".
#'
#' @param object An instance of "CNVDetectionResult"
#' @param segStat Which statistic per segment should be used. Can be either
#' "mean" or "median". (Default="mean").
#' @examples
#' data(cn.mops)
#' r <- referencecn.mops(X[,1:2],apply(X,1,median))
#' calcFractionalCopyNumbers(r)
#' @return \code{calcFractionalCopyNumbers} returns an
#' instance of "CNVDetectionResult".
#' @author Guenter Klambauer \email{klambauer@@bioinf.jku.at}
#' @export
#' @importFrom IRanges findOverlaps
#' @importFrom IRanges as.list
#' @importFrom IRanges as.matrix
#' @importFrom GenomicRanges values
setMethod("calcFractionalCopyNumbers", signature="CNVDetectionResult",
definition = function(object,segStat="mean"){
message(paste("This is an experimental function that has not",
"been tested thoroughly! Please report bugs to",
"the maintainer!"))
priorImpact <- object@params$priorImpact
cyc <- object@params$cyc
classes <- object@params$classes
I <- object@params$folds
minReadCount <- object@params$minReadCount
X <- object@normalizedData
cnvr <- object@cnvr
segmentation <- segmentation(object)
cnvs <- cnvs(object)
gr <- object@gr
cov <- object@params$cov
uT <- object@params$upperThreshold
lT <- object@params$lowerThreshold
mainClass <- object@params$mainClass
method <- object@params$method
mainCN <- 2*I[which(classes==mainClass)]
usedMethod <- switch(method,
"cn.mops"=.cn.mopsC,
"haplocn.mops"=haplocn.mopsC,
"referencecn.mops"=.referencecn.mops)
segStatI <- switch(segStat,"mean"=mean,"median"=median)
if (length(cnvr)==0 | length(cnvs)==0)
stop(paste("No CNV regions in result object. Rerun cn.mops",
"with different parameters!"))
# for CNV regions
M <- IRanges::as.list(IRanges::findOverlaps(cnvr,object@gr))
XX <- lapply(M,function(i){
if (length(i)>=3) ii <- i[-c(1,length(i))]
else ii <- i
apply(X[ii, ,drop=FALSE],2,segStatI) })
if (method=="referencecn.mops"){
lambda <- object@params$L[,mainClass]
ll <- lapply(M,function(i){
if (length(i)>=3) ii <- i[-c(1,length(i))]
else ii <- i
segStatI(lambda[ii])
})
# CN <-t(sapply(1:length(XX),function(j) {
# round(mainCN*XX[[j]]/ll[[j]],1)
# }))
alpha.prior <- rep(1,length(I))
alpha.prior[which(classes=="CN2")] <- 1+priorImpact
alpha.prior <- alpha.prior/sum(alpha.prior)
CN <-t(sapply(1:length(XX),function(j) {
paste("CN",format(
round(mainCN*2^(usedMethod(x=XX[[j]],
lambda=ll[[j]],
I=I,
classes=classes,
cov=cov,
minReadCount=minReadCount,
alpha.prior=alpha.prior,
)$sini),1),nsmall=1),sep="")
}))
} else {
stop("Only possible for referencecn.mops!")
}
CN <- matrix(CN,ncol=ncol(X))
colnames(CN) <- colnames(X)
resObject <- object
GenomicRanges::values(cnvr) <- CN
resObject@cnvr <- cnvr
## now for individual CNVs and segmentation
#mapping from CNVs to segmentation
iCN <- rep(paste("CN",format(mainCN,nsmall=1),sep=""),length(segmentation))
csM <- IRanges::as.matrix(IRanges::findOverlaps(segmentation,cnvs,type="within"))
tmpIdx <- which(IRanges::values(segmentation)$sampleName[csM[,1]]==values(cnvs)$sampleName[csM[,2]])
csM <- csM[tmpIdx, ,drop=FALSE]
M2 <- IRanges::as.data.frame(segmentation)
if (method=="referencecn.mops"){
if (segStat=="mean"){
CN2 <- paste("CN",format(round(2^(M2$mean)*mainCN,1),nsmall=1),
sep="")
} else if (segStat=="median"){
CN2 <- paste("CN",format(round(2^(M2$median)*mainCN,1),nsmall=1),
sep="")
} else {
stop("\"segStat\" must be \"mean\" or \"median\"!")
}
} else {
stop("Only possible for referencecn.mops!")
}
GenomicRanges::values(segmentation)$CN <- CN2
GenomicRanges::values(cnvs)$CN <- CN2[csM[,1]]
resObject@cnvs <- cnvs
resObject@segmentation <- segmentation
return(resObject)
})
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