computeOccupancy: Compute Occupancy values from PWM Scores based on model.

In patrickCNMartin/ChIPanalyserDev: ChIPanalyser: Predicting Transcription Factor Binding Sites

Description

computeOccupancy will compute the Occupancy from PWM Scores. As described in detail in the vignette, ChIPanalyser uses PWM Scores, DNA Accessibility data, the number of bound molecules and a sclaing factor of Transcription Factor specificty. This function will compute occupancy using the values assigned to each variable.

Usage

computeOccupancy(genomicProfiles,parameterOptions = NULL,
    norm = TRUE, verbose = TRUE)

Arguments

genomicProfiles	genomicProfiles is a a genomicProfiles object resulting from computePWMScore. IT is important to use this resulting object as the occuapancy will only be computed for sites above a threshold.
parameterOptions	parameterOptions is a parameterOptions object containing the adequate values assigned to each Parameter. If not Supplied (parameterOptions = NULL), a new object will be created internally using default values.
norm	norm a logical value which determines if the occupancy should be normalised or not.
verbose	verbose a logical value which determines if progress messages are printed or not.

Details

computeOccupancy will compute the Occupancy from PWM Scores. As described in detail in the vignette, ChIPanalyser uses PWM Scores, DNA Accessibility data, the number of bound molecules and a sclaing factor of Transcription Factor specificty. This function will compute occupancy using the values assigned to each variable. It should also be noted that the parameterOptions object contains a set of parameters used to compute Occupancy (not only restricted to this ). These parameters are often dependant on real ChIP-Seq data and will influence the goodness of fit between the predicted model an real ChIP-seq data. We strongly advise that the values assigned to each parameter should be customiszed in order to increase the model ageement with real world biological data.

Value

computeOccupancy will return a genomicProfiles. The main difference will reside in the profiles slot. This slot is generally a list or GRangesList. Within these list type structures are enclosed GRanges containing the positions of site above threshold, PWMScores and Occupancy for each site. The series of GRanges will depend on the number of loci that are tested and the number of element in the list will depend on the various combinations of lambdaPWM and boundMolecules.

Author(s)

Patrick C.N. Martin <[e-mail]>

References

Zabet NR, Adryan B (2015) Estimating binding properties of transcription factors from genome-wide binding profiles. Nucleic Acids Res., 43, 84–94.

Examples

#Data extraction
data(ChIPanalyserData)
# path to Position Frequency Matrix
PFM <- file.path(system.file("extdata",package="ChIPanalyser"),"BCDSlx.pfm")
#As an example of genome, this example will run on the Drosophila genome

if(!require("BSgenome.Dmelanogaster.UCSC.dm3", character.only = TRUE)){
    if (!requireNamespace("BiocManager", quietly=TRUE))
        install.packages("BiocManager")
    BiocManager::install("BSgenome.Dmelanogaster.UCSC.dm3")
    }
library(BSgenome.Dmelanogaster.UCSC.dm3)
DNASequenceSet <- getSeq(BSgenome.Dmelanogaster.UCSC.dm3)

#Building data objects
GPP <- genomicProfiles(PFM=PFM,BPFrequency=DNASequenceSet)
OPP <- parameterOptions()
# Computing Genome Wide
GenomeWide <- computeGenomeWideScores(genomicProfiles = GPP,
    DNASequenceSet = DNASequenceSet)

#Compute PWM Scores
PWMScores <- computePWMScore(genomicProfiles = GenomeWide,
    DNASequenceSet = DNASequenceSet,
    loci = eveLocus,
    chromatinState = Access)
#Compute Occupnacy
Occupancy <- computeOccupancy(genomicProfiles = PWMScores,
    parameterOptions = OPP)
Occupancy

patrickCNMartin/ChIPanalyserDev documentation built on Nov. 14, 2019, 4:39 p.m.