\HeaderA{xy2indices}{Functions to convert indices to x/y (and reverse)}{xy2indices}
\aliasA{indices2xy}{xy2indices}{indices2xy}
\keyword{manip}{xy2indices}
\begin{Description}\relax
Functions to convert indices to x/y (and reverse)
\end{Description}
\begin{Usage}
\begin{verbatim}
xy2indices(x, y, nr = NULL, cel = NULL, abatch = NULL, xy.offset = NULL)
indices2xy(i, nr = NULL, cel = NULL, abatch = NULL, xy.offset = NULL)
\end{verbatim}
\end{Usage}
\begin{Arguments}
\begin{ldescription}
\item[\code{x}] \code{X} position for the probes 
\item[\code{y}] \code{Y} position for the probes 
\item[\code{i}] indices in the \code{AffyBatch} for the probes 
\item[\code{nr}] total number of \code{Xs} on the chip 
\item[\code{cel}] a corresponding object of class \code{\LinkA{Cel}{Cel}} 
\item[\code{abatch}] a corresponding object of class
\code{\LinkA{AffyBatch}{AffyBatch}} 
\item[\code{xy.offset}] an eventual offset for the XY coordinates. See Details
\end{ldescription}
\end{Arguments}
\begin{Details}\relax
The probes intensities for given probe set ids are extracted from an
\code{AffyBatch} object using the indices stored in the corresponding
\code{cdfenv}.

The parameter \code{xy.offset} is there for compatibility.
For historical reasons, the xy-coordinates for the features
on Affymetrix chips were decided to start at 1 (one) rather than 0
(zero). One can set the offset to 1 or to 0. Unless the you \_really\_
know what you are doing, it is advisable to let it at the default
value \code{NULL}. This way the package-wide option code{xy.offset} is
always used.
\end{Details}
\begin{Value}
A vector of indices or a two-columns matrix of Xs and Ys.
\end{Value}
\begin{Section}{Warning}
Even if one really knows what is going on, playing with the
parameter \code{xy.offset} could be risky. Changing the package-wide
option \code{xy.offset} appears much more sane.
\end{Section}
\begin{Author}\relax
L.
\end{Author}
\begin{SeeAlso}\relax
\code{\LinkA{indexProbes}{indexProbes}}
\end{SeeAlso}
\begin{Examples}
\begin{ExampleCode}
data(affybatch.example)

pm.i <- indexProbes(affybatch.example, which="pm", genenames="AFFX-BioC-5_at")[[1]]
mm.i <- indexProbes(affybatch.example, which="mm", genenames="AFFX-BioC-5_at")[[1]]

pm.i.xy <- indices2xy(pm.i, abatch = affybatch.example)
mm.i.xy <- indices2xy(mm.i, abatch = affybatch.example)

image(affybatch.example[1], transfo=log2)
## plot the pm in red
plotLocation(pm.i.xy, col="red")
plotLocation(mm.i.xy, col="blue")

\end{ExampleCode}
\end{Examples}