[BioC] help on cdf file
Ben Bolstad
bolstad at stat.berkeley.edu
Tue Apr 19 20:13:34 CEST 2005
At least as far as rma() goes you may supply a vector of probeset names
using the subset argument. eg
library(affy);library(affydata);data(Dilution)
goodprobesets <- geneNames(Dilution)[1:10]
eset <- rma(Dilution,subset=goodprobesets)
eset
On Tue, 2005-04-19 at 13:17 -0400, Jianping Jin wrote:
> Hi All,
>
> I am interested in using a reduced number of probe sets of HG-U133plus2,
> for example masking some probe sets, to run RMA for my data analysis. I
> guess that I should make all new .CEL files from the original data sets and
> a new .cdf file which is modified to fit my new data sets. I am wondering
> if there are some easy ways with BioC to achieve that? Do I have to write
> some codes with, e.g. Perl, to make the new data sets and a new cdf?
>
> Any suggestions and help will be greatly appreciated!
>
> JP Jin
>
> xxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxx
> x Jianping Jin Ph.D. x
> x Bioinformatics scientist x
> x Center for bioinformatics x
> x 3133 Bioinformatics Building x
> x CB# 7104 x
> x University of North Carolina x
> x Chapel Hill, NC 27599 x
> x Tel: (919)843-6105 x
> x Fax: (919)843-3103 x
> x E-mail: jjin at email.unc.edu x
> xxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxx
>
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