Nothing
prepERCCDat <- function(expDat){
sampleInfo <- expDat$sampleInfo
expressDat <- expDat$Transcripts
idCols <- expDat$idCols
# get just ERCC data in the expression data frame
expressDat = expressDat[c(grep("ERCC-0", expressDat$Feature)),]
# Length normalize the Expected ERCC concentrations
kNorm = sampleInfo$kNorm
if (kNorm %in% c("N","n","no","No")){
lengthFactor = (idCols$Length) #/(1000)
ERCCxlabelIndiv <- expression(paste("Log2 ERCC Spike ",
"Amount (attomol nt ", mu,
"g"^"-1"," total RNA)", sep = ""))
ERCCxlabelAve <- expression(paste("Log2 Average ERCC Spike ",
"Amount (attomol nt ", mu,
"g"^"-1"," total RNA)", sep = ""))
}
if(kNorm %in% c("Y","y","yes","Yes")){
lengthFactor = 1
ERCCxlabelIndiv = expression(paste("Log2 ERCC Spike ",
"Amount (attomol nt ", mu,
"g"^"-1"," total RNA)", sep = ""))
ERCCxlabelAve = expression(paste("Log2 Average ERCC Spike ",
"Amount (attomol nt ", mu,
"g"^"-1"," total RNA)", sep = ""))
}
#If length normalization of the expected concentrations is desired (default)
idCols$Conc1 = (idCols$Conc1*lengthFactor)
idCols$Conc2 = (idCols$Conc2*lengthFactor)
### Calculate the per ERCC amount spiked attomoles of nt / ug total RNA
### ERCCdilution = 1; spikeVol = 50; totalRNAmass = 2.5*10^(3)
spikeFraction <- (sampleInfo$erccdilution*sampleInfo$spikeVol)/(sampleInfo$totalRNAmass)
idCols$Conc1 <- idCols$Conc1*spikeFraction
idCols$Conc2 <- idCols$Conc2*spikeFraction
expDat$idCols <- idCols
expDat$plotInfo$ERCCxlabelIndiv <- ERCCxlabelIndiv
expDat$plotInfo$ERCCxlabelAve <- ERCCxlabelAve
expDat$spikeFraction <- spikeFraction
return(expDat)
}
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