\HeaderA{flowcyt.fcs}{Flow Cytometry Standard (FCS) files from British Columbia
Cancer Research Center}{flowcyt.fcs}
\aliasA{bccrc}{flowcyt.fcs}{bccrc}
\keyword{datasets}{flowcyt.fcs}
\begin{Description}\relax
Flow Cytometry Standard (FCS) files 'FCS' objects,  using the version of
\code{read.series.FCS} in \pkg{rflowcyt} on October 1, 2005.

The data come from a screening of a compound library. The screening
was performed on a cell line. The name of one file corresponds to the
position of the sample (cell line aliquot) in a 96 wells plate.
\end{Description}
\begin{Usage}
\begin{verbatim}
## FCS files to be read with 'read.FCS' or 'read.series.FCS'
## function, see examples for details\end{verbatim}
\end{Usage}
\begin{Format}\relax
binary FCS files
\end{Format}
\begin{Source}\relax
British Columbia Cancer Research Center, Vancouver, Canada
\end{Source}
\begin{References}\relax
Gasparetto, M. \emph{et. al.} (2004) Identification of compounds
that enhance the anti-lymphoma activity of rituximab usinf flow
cytometric high-content screening, \emph{Journal of Immunollogical
Methods}, \bold{292}, 59-71.
\end{References}
\begin{Examples}
\begin{ExampleCode}

 ## Example I
 if (require(rflowcyt)) {

 ##obtaining the location of the fcs files in the data
  pathFiles <- system.file("bccrc", package="rfcdmin")
  drugFiles <- dir(pathFiles)

 ## reading in the FCS files
  drugData <- read.series.FCS(drugFiles, path=pathFiles, MY.DEBUG=FALSE)
 }

 ## Example II
 if (require(rflowcyt)) {
    ## obtaining the location of the fcs files in the data
    A06path <- paste(system.file("bccrc", package="rfcdmin"), "A06",sep="/")
    
    ## reading in the FCS files
    A06 <- read.FCS(A06path)
 }

\end{ExampleCode}
\end{Examples}

