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Rob Dunne
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230
@rob-dunne-292
Last seen 10.2 years ago
HI list,
how are people normalizing 133a and b chips?
here is what I am doing.
1) bg.correct.rma2 (so this is per chip)
2) extract the pm values for all chips
3) for each pair (A and B) get the probes in common (168 genes)
and make a linear correction factor to to correct the B chip.
4) adjust all the B chips to thir corresponding A chip
5) put the data (A and B) in a matrix and
do quantile normalization
6) this gives me the corrected probes, unfortunately some
are now negative so I add a slight fudge factor
7) I read the probes back into an AffyBatch object and get
expression values (medianpolish)
does this sound reasonable?
bye
rob
--
Rob Dunne Fax: +61 2 9325 3200 Tel: +61 2 9325 3263
CSIRO Mathematical and Information Sciences +61 2 9325 3100
Locked Bag 17, North Ryde, New South Wales, Australia, 1670
http://matilda.vu.edu.au/~dunne Email: Rob.Dunne@csiro.au
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