if (FALSE) {
library(RPPanalyzer)
data(dataI)
dataI_bgcorr <- correctBG(dataI,method="normexp")
dataIb <- pick.high.conc(dataI_bgcorr,highest="dilution")
normRow <- normalizeRPPA(dataIb,method="row")
normDye <- normalizeRPPA(dataIb,method="proteinDye")
normPassay <- normalizeRPPA(dataIb,method="extValue",useCol="concentration")
normHK <- normalizeRPPA(dataIb,method="housekeeping",normalizer="housekeeping")
}
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