[BioC] [limma] Separate Channel Analysis of 2 color data with summarization
Gordon K Smyth
smyth at wehi.EDU.AU
Wed Aug 11 01:45:55 CEST 2010
Dear Ana,
Your idea sounds reasonable in principle to me. It seems reasonable to me
that summarized values would have somewhat less tight correlation than R/G
values on the same spot, so I wouldn't be worried about an intraspot
correlation of 0.5.
Best wishes
Gordon
> Date: Mon, 9 Aug 2010 19:02:02 +0200
> From: Ana Conesa <aconesa at cipf.es>
> To: "bioconductor at stat.math.ethz.ch" <bioconductor at stat.math.ethz.ch>
> Subject: [BioC] [limma] Separate Channel Analysis of 2 color data with
> summarization
>
>
> Dear List,
>
> I am analyzing some yeast Nimblegen arrays following the separate channel
> analysis of 2 color data of the limma package. After within and between
> arrays normalization steps I did a summarization (medianpolish of M and A
> values for 12 spots/gene) step to reduce the number of features for
> differential expression analysis. My idea was then to calculate
> intraspotcorrelation and use the lmscFit function. My question is whether it
> should be OK to compute the intra spot correlation and the linear model using
> these summarized values. One result that calls my attention is that the
> intraspotcorrelation computed on the summarized values has a consensus value
> of 0.517. From other posts in the list, it has been mentioned that intraspot
> correlation should be above 0.8, so I am wondering if this approach is
> conceptually correct.
>
> Thanks for any suggestion on this topic
>
> Regards
>
> --
> Ana Conesa
> Bioinformatics and Genomics Department
> Centro de Investigaciones Principe Felipe
> Avda. Autopista Saler 16,
> 46012 Valencia, Spain
> Phone: +34 96 328 96 80
> Fax: +34 96 328 97 01
> http://bioinfo.cipf.es/aconesa
> http://www.blast2go.org
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