[BioC] VSN: narrowing down probe sets for parameter estimation
Stefan Thomsen
stt26 at cam.ac.uk
Fri Oct 19 10:22:24 CEST 2007
Dear all,
I am working on an Affymetrix time series data set with high percentages
(30-40%) and mostly downregulated differentials.
In a previous discussion regarding the question of a suitable normalization
strategy for such data sets Wolfgang Huber highly recommended to "narrow
down the probes from which you fit the parameters from all genes (incl. the
differential ones) to a subset which are enriched for non-changing."
In this context I have two questions:
1) What is the minimum number of genes/probes that should be used for VSN
parameter estimation? I could extract a list of some hundred 'stable' or
'low variability' genes from previous microarray studies. Would this number
be sufficient or do I need bigger probe subsets (thousands of probes, 1/2
of all probes, etc.)?
2) Is there a straight foward way to implement this into standard R
packages offerring VSN? In other words, if I perform a VSN parameter
estimation on my gene/probe subset, how (in R terms) would I subsequently
apply this to the whole dataset?(My apologies if this is trivial, my
programming skills are still rather a disgrace :) )
Any comment on these questions would be highly appreciated.
Kind regards,
Stefan
--
Dr. Stefan Thomsen
Research Associate
Department of Zoology
University of Cambridge
Downing Street
Cambridge CB2 3EJ
Tel.: +44 1223 336623
Fax: +44 1223 336679
stt26 at cam.ac.uk
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