R/computeChIPProfile.R

Defines functions computeChIPProfile

Documented in computeChIPProfile

#######################################################################
# Functions
#######################################################################


computeChIPProfile <- function(genomicProfiles,loci=NULL,
    parameterOptions = NULL,
    norm = TRUE, method = c("moving_kernel","truncated_kernel","exact"),
    peakSignificantThreshold = NULL,cores=1, verbose = TRUE){

    # Validity checking
    if(!is.null(loci)){
        if(is(loci,"ChIPScore")){
          chipMean(genomicProfiles)<-chipMean(loci)
          chipSd(genomicProfiles)<-chipSd(loci)
          chipSmooth(genomicProfiles)<-chipSmooth(loci)
          maxSignal(genomicProfiles)<-maxSignal(loci)
          backgroundSignal(genomicProfiles)<-backgroundSignal(loci)
          loci<-loci(loci)


        } else if(is(loci,"Granges")) {
           loci <-loci
        }
    } else {
        stop(paste("Please provide a set of loci to be analysed \n",
                   "If you have used processingChIP, you can parse that object \n",
                   "Otherwise, you can provide your own loci as a GRanges. "))
    }
    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 an parameterOptions Object."))
    }

    if(!is.null(parameterOptions)){
        genomicProfiles<-.updateGenomicProfiles(genomicProfiles,parameterOptions)
    }

    # Extraction of Ocuupancy and associated values
    Occup <- profiles(genomicProfiles)
    ZeroBackground <- .ZeroBackground(genomicProfiles)

    #Extraction of Occupancy Profile Parameters
    stepSize <- stepSize(genomicProfiles)
    backgroundSignal <- backgroundSignal(genomicProfiles)
    removeBackground <- removeBackground(genomicProfiles)
    chipMean <- chipMean(genomicProfiles)
    chipSd <- chipSd(genomicProfiles)
    dropLoci<-drop(genomicProfiles)
    if(!is.null(chipSmooth(genomicProfiles))){
        chipSmooth <- chipSmooth(genomicProfiles)
    } else {
        chipSmooth <- NULL
    }
    maxSignal <- maxSignal(genomicProfiles)


    # Extracting names of sequences with no accesible DNA

   if(length(grep("No loci dropped",dropLoci))==0){
      widthDisplay<-round(options()$width*0.5)
      cat("No Accessible DNA in: ",paste(rep(" ",
         times=(widthDisplay-nchar("StepSize: ")-nchar(dropLoci[1]))),collapse=''),
         dropLoci,"\n","\n")
    }

    # loci fragmentation
    #Spliting loci for Chip PRofile computing
    if(!is.null(loci) & is.null(names(loci))){
			  names(loci)<-paste0(seqnames(loci),":",
				start(ranges(loci)),"..",end(ranges(loci)),sep="")
		}


    LocalSet <- split(loci, names(loci))
    LocalSet <-LocalSet[match(names(Occup[[1]]),names(LocalSet))]


    #Computing Chip like profile
    if(verbose){
        message("Computing ChIP Profile \n")
    }

    SplitGRList <-parallel::mclapply(LocalSet,.internalChIPLociSplit,stepSize,mc.cores=cores)

    names(SplitGRList) <- names(LocalSet)


    ##method set
    if(length(Occup)>length(Occup[[1]])){
        OccupancyVals <- parallel::mclapply(Occup,.internalChIPOccupValsParam,mc.cores=cores)

        profile <- parallel::mcmapply(.internalChIPParam,Occup=Occup,
        OccupancyVals=OccupancyVals,
        MoreArgs=list(SplitGRList=SplitGRList,LocalSet=LocalSet,
        chipMean=chipMean,chipSd=chipSd,
        stepSize=stepSize,norm=norm,chipSmooth=chipSmooth,
        peakSignificantThreshold=peakSignificantThreshold,
        ZeroBackground=ZeroBackground,
        removeBackground=removeBackground,method=method),
        mc.cores=cores,SIMPLIFY=FALSE)
    } else {
    profile <- vector("list", length(Occup))
    OccupancyVals <- vector("list", length(Occup))
    for(i in seq_along(Occup)){
        OccupancyVals[[i]]<- parallel::mclapply(Occup[[i]],.internalChIPOccupValsLoci,mc.cores=cores)

        profile[[i]]<-SplitGRList
        profile[[i]] <- parallel::mcmapply(.internalChIPLoci,
        profile=profile[[i]],Occup=Occup[[i]],LocalSet=LocalSet,
        OccupancyVals=OccupancyVals[[i]],
        MoreArgs=list(chipMean=chipMean,chipSd=chipSd,
        stepSize=stepSize,norm=norm,chipSmooth=chipSmooth,
        peakSignificantThreshold=peakSignificantThreshold,
        ZeroBackground=ZeroBackground,
        removeBackground=removeBackground,method=method), mc.cores=cores)

    }
    }
    ### GRlist output

    profile <-lapply(profile,GRangesList)
    names(profile)<-names(Occup)

    .profiles(genomicProfiles)<-profile
    .tags(genomicProfiles)<-"ChIPProfile"
    return(genomicProfiles)

}
patrickCNMartin/ChIPanalyser documentation built on Nov. 24, 2022, 12:02 a.m.