rjmcmcCHR {RJMCMCNucleosomes} | R Documentation

## Nucleosome positioning mapping on a large segment, up to a chromosome

### Description

Use of a fully Bayesian hierarchical model for chromosome-wide profiling of nucleosome positions based on high-throughput short-read data (MNase-Seq data). Beware that for a genome-wide profiling, each chromosome must be treated separatly. This function is optimized to run on an entire chromosome.

The function will process by splittingg the `GRanges` of reads (as example, the reads from a chromosome) in a `list` of smaller `GRanges` segments that can be run by the `rjmcmc` function. All those steps are done automatically.

### Usage

    rjmcmcCHR(reads, seqName = NULL, zeta = 147, delta, maxLength,
      nbrIterations, kMax, lambda = 3, minInterval, maxInterval, minReads = 5,
      adaptIterationsToReads = TRUE, vSeed = -1, nbCores = 1,
      dirOut = "out", saveAsRDS = FALSE, saveSEG = TRUE)

### Arguments

`reads` | a `GRanges`, the forward and reverse reads that need to be segmented.
`seqName` | a `character` string containing the label of the chromosome, present in the `GRanges` object, that will be used. The `NULL` value is accepted when only one seqname is present in the `GRanges`; the only seqname present will be used. Default: `NULL`.
`zeta` | a positive `integer` or `numeric`, the length of the nucleosomes. Default: 147.
`delta` | a positive `integer` or `numeric`, the accepted range of overlapping section between segments. The overlapping section being `zeta` + `delta`.
`maxLength` | a positive `integer` or `numeric`, the length of each segment.
`nbrIterations` | a positive `integer` or `numeric`, the number of iterations. Non-integer values of `nbrIterations` will be casted to `integer` and truncated towards zero.
`kMax` | a positive `integer` or `numeric`, the maximum number of degrees of freedom per region. Non-integer values of `kMax` will be casted to `integer` and truncated towards zero.
`lambda` | a positive `numeric`, the theorical mean of the Poisson distribution. Default: 3.
`minInterval` | a `numeric`, the minimum distance between two nucleosomes.
`maxInterval` | a `numeric`, the maximum distance between two nucleosomes.
`minReads` | a positive `integer` or `numeric`, the minimum number of reads in a potential canditate region. Non-integer values of `minReads` will be casted to `integer` and truncated towards zero. Default: 5.
`adaptIterationsToReads` | a `logical` indicating if the number of iterations must be modified in function of the number of reads. Default: `TRUE`.
`vSeed` | a `integer`. A seed used when reproducible results are needed. When a value inferior or equal to zero is given, a random integer is used. Default: -1.
`nbCores` | a positive `integer`, the number of cores used to run in parallel. Default: 1.
`dirOut` | a `character` string. The name of the directory where 2 directories are created (if they don't already exists). The directory "dirOut/results" contents the rjmcmc results for each segment. The directory "dirOut/done" contents file a log file for each segment in RData format. If the log file for a segment is in the directory, the program considers that it is has been processed and run the next segment. Default: "out".
`saveAsRDS` | a `logical`. When `TRUE`, a RDS file containing the complete output of the `rjmcmc` function is created. Default: `FALSE`.
`saveSEG` | a `logical`. When `TRUE`, a RDS file containing the segments generated by `segmentation` function is saved in directory named from paramter `dirOut`. Default: `FALSE`.

### Value

a `list` of class "rjmcmcNucleosomesBeforeAndAfterPostTreatment" containing:

- k a `integer`, the number of nucleosomes.

- mu a `GRanges` containing the positions of the nucleosomes.

- kPost a `integer`, the number of nucleosomes after post-treatment and '*' as strand. The `seqnames` of the `GRanges` correspond to the `seqName` input value. `NA` when no nucleosome is detected.

- muPost a `GRanges` containing the positions of the nucleosomes after post-treament and '*' as strand. The `seqnames` of the `GRanges` correspond to the `seqName` input value. `NA` when no nucleosome is detected.

### Author(s)

Pascal Belleau, Astrid Deschenes

### Examples

    ## Load synthetic dataset of reads
    data(syntheticNucleosomeReads)

    ## Use dataset of reads to create GRanges object
    sampleGRanges <- GRanges(syntheticNucleosomeReads$dataIP)

    ## Run nucleosome detection on the entire sample
    ## Not run: result <- rjmcmcCHR(reads = sampleGRanges, zeta = 147, delta=50,
    maxLength=1200, nbrIterations = 1000, lambda = 3, kMax = 30,
    minInterval = 146, maxInterval = 292, minReads = 5, vSeed = 10113,
    nbCores = 2, saveAsRDS = FALSE)
    ## End(Not run)

[Package RJMCMCNucleosomes version 1.6.0 Index]