[BioC] LIMMA: donor effect
Gordon K Smyth
smyth at wehi.EDU.AU
Sun Apr 24 01:37:37 CEST 2011
Dear Som,
The usual way to deal with the donor effect is to include a factor for
donor in the design matrix. This ensures that all your comparisons are
made within donor:
design <- model.matrix(~Donor+Dose*Time)
Usually I would prefer to correct for the batch effect in the design
matrix, rather than pre-correcting with ComBat, because it ensures that
the degrees of freedom reflect that fact that batch correction the has
been done.
Best wishes
Gordon
> Date: Fri, 22 Apr 2011 13:49:59 -0400
> From: somnath bandyopadhyay <genome1976 at hotmail.com>
> To: <genome1976 at hotmail.com>
> Cc: bioconductor-bounces at r-project.org, bioconductor at stat.math.ethz.ch
> Subject: [BioC] LIMMA: donor effect
>
>
> I am trying to analyze microarray data for a project where whole blood
> was collected from 4 different donors and was treated with a compound at
> 2 time-points at 4 different doses. I am interested in genes that are
> differentially regulated with dose, with time and also dose*time. When I
> run a PCA on the entire data, the separation of groups is mainly by
> donors. How do I run a limma analysis (factors, design matrix) to get to
> the genes of interest (mentioned earlier)? I am not interested in genes
> that are differentially expressed across donors. Any suggestion would be
> greatly appreciated.
>
> Thanks,
> Som.
>
> Would it be O.K. to use ComBat to get rid off donor effects by treating
> each donor as a batch?
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