| atacRepsPipe | R Documentation | 
The preset pipeline to process multi-replicates case study sequencing data. HTML report files, result files(e.g. BED, BAM files) and conclusion list will generated. See detail for usage.
atacRepsPipe( genome, fastqInput1, fastqInput2 = NULL, refdir = NULL, tmpdir = NULL, threads = 2, adapter1 = NULL, adapter2 = NULL, interleave = FALSE, createReport = TRUE, motifs = NULL, prefix = NULL, chr = c(1:22, "X", "Y"), p.cutoff = 1e-06, ... )
genome | 
 
  | 
fastqInput1 | 
 
  | 
fastqInput2 | 
 
  | 
refdir | 
 
  | 
tmpdir | 
 
  | 
threads | 
 
  | 
adapter1 | 
 
  | 
adapter2 | 
 
  | 
interleave | 
 
  | 
createReport | 
 
  | 
motifs | 
 either  | 
prefix | 
 
  | 
chr | 
 Which chromatin the program will processing. It must be identical with the filename of cut site information files or subset of . Default:c(1:22, "X", "Y").  | 
p.cutoff | 
 p-value cutoff for returning motifs, default: 1e-6.  | 
... | 
 Additional arguments, currently unused.  | 
List scalar. It is a list that save the result of the pipeline.
Slot "filelist": the input file paths.
Slot "wholesummary": a dataframe that for quality control summary
Slot "atacProcs": ATACProc-class objects generated by each process in the pipeline.
Slot "filtstat": a dataframe that summary the reads filted in each process.
Zheng Wei and Wei Zhang
printMap,
atacPipe2,
atacRenamer,
atacRemoveAdapter,
atacBowtie2Mapping,
atacPeakCalling,
atacMotifScan
## Not run: 
## These codes are time consuming so they will not be run and
## checked by bioconductor checker.
# call pipeline
# for a quick example(only CTCF and BATF3 will be processing)
conclusion <-
  atacRepsPipe(
       # MODIFY: Change these paths to your own case files!
       # e.g. fastqInput1 = "your/own/data/path.fastq"
       fastqInput1 = list(system.file(package="esATAC", "extdata", "chr20_1.1.fq.gz"),
                          system.file(package="esATAC", "extdata", "chr20_1.2.fq.bz2")),
       fastqInput2 = list(system.file(package="esATAC", "extdata", "chr20_2.1.fq.gz"),
                          system.file(package="esATAC", "extdata", "chr20_2.2.fq.bz2")),
       # MODIFY: Set the genome for your data
       genome = "hg19",
       motifs = getMotifInfo(motif.file = system.file("extdata", "CustomizedMotif.txt", package="esATAC")))
# call pipeline
# for overall example(all vertebrates motif in JASPAR will be processed)
conclusion <-
  atacRepsPipe(
       # MODIFY: Change these paths to your own case files!
       # e.g. fastqInput1 = "your/own/data/path.fastq"
       fastqInput1 = list(system.file(package="esATAC", "extdata", "chr20_1.1.fq.gz"),
                          system.file(package="esATAC", "extdata", "chr20_1.2.fq.bz2")),
       fastqInput2 = list(system.file(package="esATAC", "extdata", "chr20_2.1.fq.gz"),
                          system.file(package="esATAC", "extdata", "chr20_2.2.fq.bz2")),
       # MODIFY: Set the genome for your data
       genome = "hg19")
## End(Not run)
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