Dan Strumpf wrote:
> I am new to exon array analysis and have used the
> package (downloaded from
> )as a cdf source/mapping for processing Human exon array data within
> package. Processing went smoothly without any error messages.
> communication about this package in Oct. 2007, and am not clear if
> using it are relaible.
I don't know anything about that cdf, but if it is similar to the
modified cdf that you can get from PICR for exonmap, you should get
pretty much the same values, as exonmap uses the affy package and a
modified cdf to compute expression values.
The upside to using exonmap is that you have ways to map the probesets
to their location on the genome, and could thereby filter out those
hit what are considered to be inter-genic or intronic positions.
I don't know if you will be able to use gcrma, as there are no MM
on the exon chips. Instead they just have two sets of probes that are
designed to measure background.
> I am interested in processing Human exon array data also with gcRMA
> wondering if should use the above package or use xps/exonmap/oligo
> Would like to know also what are to options for differential
> analysis equivalent to samr limma or RankProd for paired samples
> exon array analysis packages or could the preprocessed/normalized
> exported and used with xps/exonmap/oligo packages.
Pre-processing and differential expression are in general handled by
different packages. For instance, you don't use the affy or gcrma
package to look for differentially expressed genes, and the same holds
true for xps, exonmap, and oligo.
That said, there isn't really that much different between the exon
data and the 3' biased arrays, so tools like limma and RankProd should
be fine for analyzing these data.
> Bioconductor mailing list
> Bioconductor at stat.math.ethz.ch
> Search the archives:
James W. MacDonald, M.S.
8220D MSRB III
1150 W. Medical Center Drive
Ann Arbor MI 48109-5646