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Steve Taylor
▴
280
@steve-taylor-2838
Last seen 10.3 years ago
Hi,
I have two sets of affy data CEL files. One set is from Hugene 1.0 ST
arrays and the other from U133plus2 Arrays. I need to compare one set
with another.
First I plan to use RMA to normalise the data set for each platform. I
then plan to get a common reference id across the arrays, probably
using ENSEMBL gene ID.
With the subset that have probes in common, what would be the best way
to normalise across the arrays? Would quantile normalization using
aroma.light be suitable?
Thanks for any advice,
Steve
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Medical Sciences Division
Weatherall Institute of Molecular Medicine/Sir William Dunn School
Oxford University