ExoDataSubsampling: ExoDataSubsampling
In ChIPexoQual: ChIPexoQual

Description Usage Arguments Value Examples

ExoDataSubsampling samples sample.reads from the ChIP-exo experiment and creates a list of ExoData objects

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ExoDataSubsampling(file = NULL, reads = NULL, sample.depth = NULL,
  height = 1, nregions = 1000, ntimes = 1000, verbose = TRUE,
  save.reads = FALSE, mc.cores = getOption("mc.cores", 2L))

`file`	a character value with location of the bam file with the aligned reads.
`reads`	a `GAlignments` object with the aligned reads of a ChIP-exo sample. It is meant to be used instead of `file`.
`sample.depth`	a numeric vector with the number of reads to be sampled.
`height`	a numeric value indicating the value used to slice the coverage of the experiment into a set of regions.
`nregions`	a numeric value indicating the number of regions sampled to estimate the quality parameter distributions. The default value is 1e3.
`ntimes`	a numeric value indicating the number of times that regions are sampled to estimate the quality parameter distributions. The default value is 1e2.
`verbose`	a logical value indicating if the user want to receive progress details. The default value is FALSE.
`save.reads`	a logical value to indicate if the reads are stored in the `ExoData` object. The default value is `FALSE`.
`mc.cores`	a numeric value with the number of cores to use, i.e. at most how many child processes will be run simultaneously.

It returns an ExoData object with the regions obtained after partitioning the genome and the summary statistics for each region. If the save.reads parameter is TRUE then it contains a GRanges object with the reads of the ChIP-exo experiment.

files <- list.files(system.file("extdata",package = "ChIPexoQualExample"),
    full.names = TRUE)
sample.depth <- seq(1e5,2e5,5e4)
ExoDataSubsampling(file = files[5],sample.depth = sample.depth)