\name{scores2calls} \alias{scores2calls} \title{Sigmoidal transformation of the score values stored in a cellHTS object obtaining the call values for each probe.} \description{ Apply a sigmoidal transformation with parameters z0 and lambda to the summarized scored values stored in a \code{\linkS4class{cellHTS}} object. The obtained results are called \emph{calls} and are stored in slot \code{assayData}, overridding its current content. Currently this function is implemented only for single-color data. } \usage{ scores2calls(x, z0, lambda) } \arguments{ \item{x}{an object of class \code{\linkS4class{cellHTS}} containing replicate data that have already been scored and summarized (see details).} \item{z0}{a numeric value giving the centre of the sigmoidal transformation. See details.} \item{lambda}{a numeric value (>0) that corresponds to the parameter \code{lambda} of the sigmoidal transformation. This value should be \code{>0}, but usually it makes more sense to use a value \code{>=1}. See details.} } \details{ This function applies a sigmoidal transformation with parameters z0 and lambda to the single per-probe score values stored in a \code{cellHTS} object. The obtained results are called \emph{calls}. The transformation is given by: \deqn{1 / (1 + exp(-lambda * (z- z0)))} where \code{z} are the score values, \code{z0} is the centre of the sigmoidal transformation, and the \code{lambda} is a parameter that controls the smoothness of the transformation. The higher is \code{lambda}, more steeper is the transition from lower to higher values. \code{lambda} should be \code{> 0}, but usually it makes more sense to use a value \code{>=1}. This transformation maps the score values to the interval \code{[0,1]}, and is intended to expand the scale of scores with intermediate values and shrink the ones showing extreme values, therefore making the difference between intermediate phenotypes larger. } \value{ The \code{cellHTS} object with the call values stored in slot \code{assayData}. This is an object of class \code{assayData} corresponding to a single matrix of dimensions \code{Features x 1}. } \seealso{ \code{\link[cellHTS2:normalizePlates]{normalizePlates}}, \code{\link[cellHTS2:summarizeChannels]{summarizeChannels}}, \code{\link[cellHTS2:scoreReplicates]{scoreReplicates}}, \code{\link[cellHTS2:summarizeReplicates]{summarizeReplicates}}, \code{\link[cellHTS2:imageScreen]{imageScreen}}. } \references{ Boutros, M., Bras, L.P. and Huber, W. (2006) Analysis of cell-based RNAi screens, \emph{Genome Biology} \bold{7}, R66. } \author{W. Huber \email{huber@ebi.ac.uk}, Ligia Braz \email{ligia@ebi.ac.uk}} \examples{ data(KcViabSmall) x <- normalizePlates(KcViabSmall, scale="multiplicative", method="median", varianceAdjust="none") x <- scoreReplicates(x, sign="-", method="zscore") x <- summarizeReplicates(x, summary="min") xc <- scores2calls(x, z0=1.5, lambda=2) plot(Data(x), Data(xc), col="blue", xlab="z-scores", ylab="calls", main=expression(1/(1+e^{-lambda *(z-z[0])}))) if(require(splots)) { sp = split(Data(xc), plate(xc)) grid.newpage() plotScreen(sp, zrange=c(0,1), fill=c("white", "red"), na.fill="yellow", main="Calls", ncol=3L) } } \keyword{manip}