profileAccuracyEstimate: Estimating Accuracy of predicted Profiles

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

Description

profileAccuracyEstimate will compare the predicted ChIP-seq-like profile to real ChIP-seq data and return a set of metrics describing how accurate the predicted model is compared to real data.

Usage

  profileAccuracyEstimate(genomicProfiles,ChIPScore,
      parameterOptions=NULL,method="all",cores=1)

Arguments

genomicProfiles	genomicProfiles is the result of computeChIPProfile
ChIPScore	ChIPScore is the result of processingChIP. Extracted/Normalised experimental ChIP scores.
parameterOptions	parameterOptions is a parameterOptions object for paramter specification.
method	method is the method that will be used to assess model quality agianst ChIP-seq data. Method can be one of the following: pearson, spearman, kendall, ks, geometric,fscore, MSE,or all.Fscore contains f-score, precision,recall, MCC, Accuracy and AUC ROC.
cores	cores is the number of cores used to extract ChIP scores. Default = 1

Details

In order to assess the quality of the model against experimental ChIP-seq data, ChIPanalyser offers a wide range of method to choose from. These methods are also used when computing optimal paramters.

Value

Returns list of goodness of fit metrics for each loci and each parameter selected.

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 genomicProfiles object
  GPP <- genomicProfiles(PFM=PFM, BPFrequency=DNASequenceSet)


  # Computing Genome Wide
  GenomeWide <- computeGenomeWideScore(genomicProfiles = GPP,
      DNASequenceSet = DNASequenceSet)

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

  #Compute ChIP profiles
  chipProfile <- computeChIPProfile(genomicProfiles=Occupancy,loci=eveLocus)
#Estimating accuracy estimate
AccuracyEstimate <- profileAccuracyEstimate(genomicProfiles = chipProfile,
    ChIPScore = eveLocusChip,
    occupancyProfileParameters = OPP)

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