inst/testScripts/system/chipTypes/Cytogenetics_Array/test20090828,cyto.R

library("aroma.affymetrix")
verbose <- Arguments$getVerbose(-50, timestamp=TRUE)


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# Setup
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dataSet <- "Affymetrix-CytoSampleData"
chipType <- "Cytogenetics_Array"

cdf <- AffymetrixCdfFile$byChipType(chipType)
print(cdf)

csR <- AffymetrixCelSet$byName(dataSet, cdf=cdf)
print(csR)


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# Allelic-crosstalk calibration
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acc <- AllelicCrosstalkCalibration(csR)
print(acc)
csC <- process(acc, verbose=verbose)
print(csC)


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# Plot allele pairs before and after calibration
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for (what in c("input", "output")) {
  toPNG(getFullName(acc), tags=c("allelePairs", what), aspectRatio=0.7, {
    plotAllelePairs(acc, array=1, what=what, verbose=verbose)
  })
}


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# Probe-level summarization
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plm <- AvgSnpPlm(csC, mergeStrands=TRUE)
print(plm)
if (length(findUnitsTodo(plm)) > 0) {
  # Fit CN probes quickly (~5-10s/array + some overhead)
  units <- fitCnProbes(plm, verbose=verbose)
  str(units)
  # int [1:2377527] 401698 401699 401700 401701 401702 401703 ...

  # Fit remaining units, i.e. SNPs (~5-10min/array)
  units <- fit(plm, verbose=verbose)
  str(units)
  # int [1:418181] 1 2 3 4 5 6 7 8 9 10 ...
}

ces <- getChipEffectSet(plm)
print(ces)


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# Export (theta, beta) for all arrays
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dsList <- exportTotalAndFracB(ces, verbose=verbose)
print(dsList)


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# TCN Segmentation and plotting
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cns <- CbsModel(dsList$total)
print(cns)

ce <- ChromosomeExplorer(cns, zooms=2^(0:5))
print(ce)
process(ce, chromosomes=c(19, 22, 23), verbose=verbose)
HenrikBengtsson/aroma.affymetrix documentation built on Feb. 20, 2024, 9:07 p.m.