[BioC] Replicates array
Johannes Freudenberg
mai98ftu at studserv.uni-leipzig.de
Wed Mar 10 14:17:33 MET 2004
Hi Paola,
For preprocessing I would suggest to use RMA (i.e. RMA background correction +
quantile normalization + medianpolish) or VSN + medianpolish. I would normalize
all 6 arrys together. I don't think it's a good idea to normalize the two
groups separately.
> Should I just compare the differentially expressed genes lists coming
> from the two different group of duplicates??
I don't understand. Wouldn't it be just one list?
Johannes
Quoting Paola Sgado' <sgadop at yahoo.it>:
> Hi
> I just started to work with oligonucleotide microarray and I would like
>
> to have suggestions on the methods I should use to analyse the data.
>
> I have three duplicates done in two different places, so they look very
>
> different in terms of background and signal intensities. Since I'm not
> going to have more duplicates I would like to get the most information
> possible from these, even if I do know that it is not the perfect
> experimental design!
>
> My question is, if the chips are very different, should I normalize
> them separately (for example make to groups)? Does it make sense to
> compare them between two gruops if they are normalised separately?
> Should I just compare the differentially expressed genes lists coming
> from the two different group of duplicates??
>
> Thank you for your help!!
> Paola
>
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