R/base_multihistoneProcess.R

In yezhengSTAT/permseq_0.3.0: Mapping protein-DNA interactions in highly repetitive regions of the genomes with prior-enhanced read mapping

.multihistoneProcess = function(histoneFile, fragL, AllocThres, chrList, chrom.ref, capping, outfileLoc="./", outfile, bowtieIndex, csemDir, picardDir, bowtieDir, vBowtie, mBowtie, pBowtie, bwaDir, bwaIndex, nBWA, oBWA, tBWA, mBWA, saveFiles){

  #make sure the output folder is created
  if(!file.exists(outfileLoc)){
    system(paste('mkdir ',outfileLoc,sep=''))
  }
  setwd(outfileLoc)

  #find out the input format of histone. SAM/BAM/BED input format can save time by skipping the alignment process
  histoneFormat <- tolower(sub(".*\\.", "", histoneFile))
  
  # Define filenames and extensions
  filename <- strsplit(histoneFile, "/")[[1]]
  filename <- filename[length(filename)]
  filename <- strsplit(filename, paste('.', sub(".*\\.", "", filename), sep=''))[[1]][1]
  file.sai <- paste(filename, '.sai', sep='')
  file.sam <- paste(filename, '.sam', sep='')
  file.bam <- paste(filename, '.bam', sep='')
  file.bed <- paste(filename, '.bed', sep='')
  file.bed_AllocThres <- paste(filename, '_', AllocThres, '.bed', sep='')
  
  # Deal with different Histone file formats (fastq, sam, bam or bed)
  if(histoneFormat != "bed"){
    if(histoneFormat != "bam"){
      if(histoneFormat != "sam"){#Histone file is in fastq format: align-CSEM allocate multi-reads
        if(!is.null(bowtieIndex)){#Provided bowtie Index will align using bowtie
          message( "Info: Aligning histone reads using Bowtie." )
          ## Generates SAM file
          system(paste(bowtieDir, '/bowtie -q -v ', vBowtie, ' -a -m ', mBowtie, ' -p ', pBowtie, ' --sam ', bowtieIndex, ' ', histoneFile, ' ', file.sam, " 2>&1 | tee ", outfileLoc, "/priorProcessHistoneBowtie_temp.txt", sep='')) 
          
        }else{
          message( "Info: Aligning histone reads using BWA." )
          ## Generates the SAM file
          system(paste(bwaDir, '/bwa aln -n ', nBWA, ' -o ', oBWA, ' -t ', tBWA, ' ', bwaIndex, ' ', histoneFile, ' >', file.sai, sep=''))
          system(paste(bwaDir, '/bwa samse -n ', mBWA, ' ', bwaIndex, ' ', file.sai, ' ', histoneFile, ' >', file.sam, '.multiOneLine', sep=''))

          system(paste("awk '{split($0, tag,\"XA\");split($1, head, \"\"); if (head[1] == \"@\") print $0; else if ($5 >24) print $0; else if (tag[2] != \"\") print $0;}' ", file.sam, ".multiOneLine | ", bwaDir, "/xa2multi.pl >", file.sam, ".tmp", sep = ""))
          
          system(paste("cat ", file.sam, ".tmp | awk 'BEGIN {FS=\"\\t\" ; OFS=\"\\t\"} ! /^@/ && $6!=\"*\" { cigar=$6; gsub(\"[0-9]+D\",\"\",cigar); n = split(cigar,vals,\"[A-Z]\"); s = 0; for (i=1;i<=n;i++) s=s+vals[i]; seqlen=length($10) ; if (s!=seqlen) {print $0} }' >", file.sam, ".tmp.badCIGAR", sep = ""))

          system(paste("if [ $(cat ", file.sam, ".tmp.badCIGAR | wc -l) -gt 0 ]; then\ncat ", file.sam, ".tmp  | grep -v -F -f ", file.sam, ".tmp.badCIGAR >", file.sam, "\nelse\nmv ", file.sam, ".tmp ", file.sam, "\nfi", sep = "")) 

          


          ## system(paste(bwaDir, '/bwa samse -n ', mBWA, ' ', bwaIndex, ' ', file.sai, ' ', histoneFile, ' | ', bwaDir, '/xa2multi.pl >', file.sam, sep=''))

        }
        
      }else{#Histone file is in SAM format - can skip alignment step and directly allocate multi-reads using CSEM
        
        print(paste("Histone file ", histoneFile, " is in SAM format. The preprocessed aligned SAM file should contain multi-mapping reads. Otherwise, please provide FASTQ format Histone file.", sep = ""))
        file.sam <- histoneFile
      }

      ## Get chrList from SAM file
      if(length(chrList) == 0){ 
        con <- file(file.sam, open = "r") 
        chrList <- c()
        n <- 1
        while(substring(oneLine <- readLines(con, n=1, warn = FALSE), 1, 3) != "@PG"){
          if(grepl("SN", oneLine)){
            chrList[n] <- gsub('.*SN:(.*)\t.*', '\\1', oneLine)
            n <- n+1
          } 
        }
      }
      ## Remove duplicates from SAM file
      if(!is.null(picardDir)){
          CMD <- "mkdir -p TMP_permseq"
          system(CMD)
          CMD <- paste("java -Djava.io.tmpdir=TMP_permseq -jar ", picardDir, " SortSam I=", file.sam, " O=", filename, ".sort.sam VALIDATION_STRINGENCY=LENIENT SORT_ORDER=coordinate TMP_DIR=TMP_permseq", sep = "")
          system(CMD)
          CMD <- paste("java -Djava.io.tmpdir=TMP_permseq -jar ", picardDir, " MarkDuplicates I=", filename, ".sort.sam ", "O=", filename, ".nodup.sam METRICS_FILE=QCmetric VALIDATION_STRINGENCY=LENIENT ASSUME_SORTED=true REMOVE_DUPLICATES=true TMP_DIR=TMP_permseq", sep = "")
          system(CMD)
          CMD <- paste("java -Djava.io.tmpdir=TMP_permseq -jar ", picardDir, " SortSam I=", filename, ".nodup.sam O=", filename, ".nodup.sort.sam VALIDATION_STRINGENCY=LENIENT SORT_ORDER=queryname TMP_DIR=TMP_permseq", sep = "")
          system(CMD)
          CMD <- "rm -rf TMP_permseq"
          system(CMD)

      }else{
          CMD <- paste(csemDir, "/sam/samtools view -Sb -h ", file.sam ," >", filename, ".tmp.bam", sep = "")
          system(CMD)
          CMD <- paste(csemDir, "/sam/samtools sort ", filename, ".tmp.bam ", filename, ".tmp.sort", sep = "")
          system(CMD)
          
          CMD <- paste(csemDir, "/sam/samtools rmdup -s ", filename, ".tmp.sort.bam ", filename, ".tmp.nodup.bam", sep = "")
          system(CMD)
          CMD <- paste(csemDir, "/sam/samtools sort -n ", filename, ".tmp.nodup.bam ", filename, ".nodup.sort", sep = "")
          system(CMD)
          CMD <- paste(csemDir, "/sam/samtools view -h -F 0x4 ", filename, ".nodup.sort.bam >", filename, ".nodup.sort.sam", sep = "")
          system(CMD)

#                CMD <- paste("rm -rf ", filename, ".tmp*",  sep = "")
#                system(CMD)
      }
      file.sam <- paste(filename, ".nodup.sort.sam", sep = "")
      
            
      message("Info: Allocating Histone multi-reads using CSEM")
      if(!is.null(bowtieIndex)){

        system(paste(csemDir, "/run-csem --sam -p ", pBowtie, ' ', file.sam, ' ', fragL, ' ', filename, sep=''))

      }else{

        system(paste(csemDir, "/run-csem --sam -p ", tBWA, ' ', file.sam, ' ', fragL, ' ', filename, sep=''))

      }


    }else{#Histone file is in BAM format - It is better to be the CSEM alignment results
       print(paste("Histone file ", histoneFile, " is in SAM format. The preprocessed aligned BAM file should contain multi-mapping reads allocated by CSEM. Otherwise, please provide FASTQ format Histone file.", sep = ""))
       file.bam <- histoneFile
     }

    message( "Info: Transfering Histone multi-reads alignment bam file into bed file using CSEM" )
    system(paste(csemDir,"/csem-generate-input --bed ", file.bam,' ', filename, sep='')) 
  
  }else{#Histone file is BED format
    print(paste("Histone file ", histoneFile, " is in SAM format. The preprocessed aligned BED file should contain multi-mapping reads allocated by CSEM. Otherwise, please provide FASTQ format Histone file.", sep = ""))
    file.bed <- histoneFile

  }
        

   ## If it wasn't created before or given by the user, creates chrList from the bed file
  if(length(chrList) == 0){
    system(paste("awk '{print $1}' ", file.bed, " | sort | uniq > ", outfileLoc, "/chrList_temp", sep=""))
    chrList <- read.table(paste(outfileLoc, "/chrList_temp", sep=""))$V1
    system(paste("rm -rf ", outfileLoc, "/chrList_temp", sep=""))
  }

  # Filter out the alignments with posterior probability < AllocThres/1000
  system(paste("awk '$5 > ", AllocThres, " {print $0}' ", file.bed,">", file.bed_AllocThres, sep=""))
  
  message( "Info: Reading the aligned read file and processing it into nucleotide-level files..." )
  .constructNeucleotideLevelCounts(outfileLoc, file.bed_AllocThres, fragL, outfileLoc, chrList, capping)
  countfile <- paste('_', file.bed_AllocThres, '_fragL', fragL, '_bin1.txt', sep='')
  
  message( "Info: Partitioning genome(Histone)..." )
  r <- .clusterPositions_histoneonly(countfile, chrList, outfileLoc, chrom.ref, outfile)
  histoneKnots <- r[[1]]
  histoneThres <- r[[2]]

  link_tri <- link <- vector('list', length(chrList))
  names(link_tri) <- names(link) <- chrList
  for(i in chrList){
    link[[i]] <- paste(outfileLoc, '/', i, '_', outfile, '_positions_cluster.txt', sep='')
    link_tri[[i]] <- paste(outfileLoc, '/', i, '_', outfile, '_positions_3cluster.txt', sep='')
  }

  # Remove files if saveFiles=FALSE
  if(saveFiles=='FALSE' | saveFiles=='F')
  {
    #system(paste("rm -rf ", file.bam, sep = ""))
    #system(paste("rm -rf ", file.sam, sep = ""))
    system(paste("rm -rf *sorted.bam*", sep = ""))
    #system(paste("rm -rf ", '*_', AllocThres,'.bed*', sep = ""))
    #system(paste("rm -rf *_output_Dnasequantile.txt*", sep = ""))
  }

  priorObject <- list(histoneKnots = histoneKnots, histoneThres = histoneThres, posLoc_bychr = link, posLoc3_bychr = link_tri, chrList = chrList)
  return(priorObject)
}