inst/testScripts/system/chipTypes/Mapping10K_Xba142/22.doASCRMAv2,PSCN.R

library("aroma.affymetrix")
verbose <- Arguments$getVerbose(-8, timestamp=TRUE)

csR <- AffymetrixCelSet$byName("GSE8605", chipType="Mapping10K_Xba142")
print(csR)

cesN <- doASCRMAv2(csR, arrays=1:6, drop=FALSE, verbose=verbose)$cesN
print(cesN)

ceR <- getAverage(cesN, verbose=verbose)
ce <- cesN[[1]]

ugp <- getAromaUgpFile(csR)
print(ugp)

for (chr in getChromosomes(ugp)) {
  units <- getUnitsOnChromosome(ugp, chr)
  pos <- getPositions(ugp, units=units) / 1e6
  thetaR <- extractTotalAndFreqB(ceR, units=units)[,"total"]
  data <- extractTotalAndFreqB(ce, units=units)
  data[,"total"] <- 2*data[,"total"] / thetaR

  chrTag <- sprintf("Chr%02d", chr)
  toPNG(getFullName(cesN), tags=c(getFullName(ce), chrTag, "TCN"), aspectRatio=1, {
    layout(matrix(1:2, ncol=1))
    par(mar=c(3,4,2,1)+0.1, pch=".")

    # TCN tracks
    cn <- RawCopyNumbers(data[,"total"], pos, chromosome=chr)
    plot(cn, col="gray", cex=0.8, ylim=c(0,4))
    cnS <- gaussianSmoothing(cn, xOut=seq(xMin(cn), xMax(cn), by=1/2), sd=1)
    points(cnS, col="black")
    stext(side=3, pos=0, getName(ce))
    stext(side=3, pos=1, chrTag)

    # BAF tracks
    plot(pos, data[,"freqB"], cex=3, ylim=c(0,1))
    box(col="blue")
    stext(side=3, pos=0, getTags(cesN, collapse=","))
  })
} # for (chr ...)

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aroma.affymetrix documentation built on July 18, 2022, 5:07 p.m.