Sets fluorescence data vectors to RDML object

Sets fluorescence data vectors to RDML object for specified method of experiment.

Arguments

data	matrix containing in the first column data corresponding to all fluorescence values in the following columns. The name of the first column is the name of variable and names of other column are fdata.names (links to rows at description).
description	output from AsTable function that describes fluorescence data.
fdata.type	'adp' for qPCR, 'mdp' for melting data.

Examples

if (FALSE) {
PATH <- path.package("RDML")
filename <- paste0(PATH, "/extdata/", "stepone_std.rdml")
cfx96 <- RDML$new(filename)
## Use plotCurves function from the chipPCR package to 
## get an overview of the amplification curves
library(chipPCR)
## Extract all qPCR data 
tab <- cfx96$AsTable()
tab2 <- tab
tab2$run.id <- "cpp"
cfx96.qPCR <- as.data.frame(cfx96$GetFData(tab))
cpp <- cbind(cyc = cfx96.qPCR[, 1],
 apply(cfx96.qPCR[, -1], 2, 
   function(y) CPP(x = cfx96.qPCR[, 1], y = y)$y.norm))
cfx96$SetFData(cpp, tab2)
library(ggplot2)
library(gridExtra)
cfx96.gg <- cfx96$GetFData(tab, long.table = TRUE)
cpp.gg <- cfx96$GetFData(tab2,
                         long.table = TRUE)
plot1 <- ggplot(cfx96.gg, aes(x = cyc, y = fluor,
                group=fdata.name)) +
                 geom_line() +
                 ggtitle("Raw data")
plot2 <- ggplot(cpp.gg, aes(x = cyc, y = fluor,
                group=fdata.name)) +
                 geom_line() +
                 ggtitle("CPP processed data")
grid.arrange(plot1, plot2, nrow=2)
}