#######################################################################
# Functions profile Accuracy
#######################################################################
profileAccuracyEstimate <- function(genomicProfiles,ChIPScore,
parameterOptions=NULL,method="all",cores=1){
#Validity checking
if(!.is.genomicProfiles(genomicProfiles)){
stop(paste0(deparse(substitute(genomicProfiles)),
" is not a Genomic Profiles Object"))
}
if(!.is.parameterOptions(parameterOptions) &
!is.null(parameterOptions)){
stop(paste0(deparse(substitute(parameterOptions)),
" is not a parameterOptions Object."))
}
if(class(ChIPScore)!="ChIPScore" &
!is.null(ChIPScore)){
stop(paste0(deparse(substitute(ChIPScore)),
" is not a ChIPScore Object."))
}
if(!is.null(parameterOptions)){
genomicProfiles<-.updateGenomicProfiles(genomicProfiles,parameterOptions)
}
#If Sites are not accesible or have no overlapp with chipprofile
dropLoci<-drop(genomicProfiles)
if(dropLoci!="No loci dropped"){
widthDisplay<-round(options()$width*0.5)
cat("No Accessible DNA in: ",paste(rep(" ",
times=(widthDisplay-nchar("StepSize: ")-nchar(dropLoci[1]))),collapse=''),
dropLoci,"\n","\n")
}
## Extract and reorder
predictionSet<-profiles(genomicProfiles)
ValidationSet<-scores(ChIPScore)
stepSize <- stepSize(genomicProfiles)
GoF<-.cleanGoF(predictionSet,ValidationSet,stepSize)
## paralle : choosing which one to split over
if(length(predictionSet) > length(ValidationSet)){
GoF<-parallel::mclapply(GoF,.GoFPred,method,step=stepSize,mc.cores=cores)
}else{
GoF <-lapply(GoF,.GoFLoci,method=method,step=stepSize, cores=cores)
}
### computing mean over all regions
GoF <- lapply(GoF,.meanGoFScore)
.profiles(genomicProfiles)<-GoF
.tags(genomicProfiles)<-"GoF"
return(genomicProfiles)
}
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