[BioC] Data sets conducted in different labs

[donghu at itsa.ucsf.edu]

Since there is clear difference in data from two labs, I would explore
these issue first:

Did the two labs use the same type of scanner, the same reagent, the same 
amout of starting RNA?  Is the RNA quality from the two labs comparable, etc.?

Donglei Hu

On Tue, 19 Oct 2004 13:55:46 -0700 (PDT) "Fangxin Hong" wrote:

> Hi there;
> I am sorry if my question doesn't qualify for BioC mail list.
> 
> Have you met the situation that two labs carried out the same/similar
> experiment, but came out with quite different results in term of
> differentially expressed genes identified.  Have anyone  had done the
> studies on this problem, any reference/observations?
> 
> The usual way is to identify genes based on two lab's data, respectively, 
> then compare the results. What about make one model for the combined data
> from two labs which takes lab as one potential factor. In this case, how
> to do the pre-processing part, normalize all data together or two lab's
> data separately? Any recommendations?
> 
> What I observed is: I observed clearly systematic difference in the data
> from two lab. But after I normalize all data ( I used rma )together, you
> still can tell the different origin of the data after normalization, and
> the model test (limma) that the lab factor is significant for about 50%
> genes. My question is: in this case (normalize all data together), should
> I include the lab as one factor? It seems normalizing procedure can't
> cancel lab effects.
> 
> But if I normalize two lab's data separately, they will have different
> variation. Even with a lab factor, I can't use model two lab's data into
> one model.
> 
> Any comments/suggestions will be appreciated.
> 
> Bests;
> Fangxin
> 
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