[BioC] design a modelMatrix with no common references
Robert Castelo
robert.castelo at upf.edu
Mon Jul 13 11:59:38 CEST 2009
James, Guisy,
if you let me make a question about what you're discussing.
why do you say that the two-color 2x2 factorial design without a common
reference RNA source is "a lot of work" ??
(i was actually wondering how would be the 11.5 example of the Limma
user's guide without a common RNA source)
thanks!
robert.
On Fri, 2009-07-10 at 10:14 -0400, James W. MacDonald wrote:
> Hi Guisy,
>
> You really have two different experiments here, so I don't know if limma
> is going to want to do things automatically for you without warnings or
> incorrect model matrices. However, I think you want to use the
> parameters argument to modelMatrix() rather than the ref argument (since
> you have two different reference samples).
>
> > targets <- matrix(paste(rep(c("Myc","Rag"), each=4),
> rep(c("CD3","PBS"), each=2, times=3)[2:9], sep = "_"), byrow=T, ncol=2)
> > targets
> [,1] [,2]
> [1,] "Myc_CD3" "Myc_PBS"
> [2,] "Myc_PBS" "Myc_CD3"
> [3,] "Rag_CD3" "Rag_PBS"
> [4,] "Rag_PBS" "Rag_CD3"
> > colnames(targets) <- c("Cy3","Cy5")
> > rownames(targets) <- paste("Array", 1:4)
> > targets
> Cy3 Cy5
> Array 1 "Myc_CD3" "Myc_PBS"
> Array 2 "Myc_PBS" "Myc_CD3"
> Array 3 "Rag_CD3" "Rag_PBS"
> Array 4 "Rag_PBS" "Rag_CD3"
> > parameters <- cbind(First=c(-1,1,0,0), Second=c(0,0,-1,1))
> > rownames(parameters) <- c("Myc_PBS","Myc_CD3","Rag_PBS","Rag_CD3")
> > parameters
> First Second
> Myc_PBS -1 0
> Myc_CD3 1 0
> Rag_PBS 0 -1
> Rag_CD3 0 1
> > modelMatrix(targets, parameters)
> Found unique target names:
> Myc_CD3 Myc_PBS Rag_CD3 Rag_PBS
> First Second
> Array 1 -1 0
> Array 2 1 0
> Array 3 0 -1
> Array 4 0 1
> Warning message:
> In modelMatrix(targets, parameters) :
> number of parameters should be one less than number of targets
>
> But that seems like a lot of work, as the parameters matrix is exactly
> the model matrix you want.
>
> Best
>
> Giusy Della Gatta wrote:
> > Hi everybody,
> >
> > I have Agilent two colors expression arrays in which have been analyzed
> > two KO mice samples (myc-/- and Rag -/-) treated with CD3 and with PBS.
> > I have a total of 4 arrays composed as follows:
> > Sample Cy3 Cy5
> > 1. Myc24CD3 Myc_CD3 Myc_PBS (Swap)
> > 2. Myc24PBS Myc_PBS Myc_CD3
> > 3. Rag24CD3 Rag_CD3 Rag_PBS (Swap)
> > 4. Rag24PBS Rag_PBS Rag_CD3
> >
> > After the normalization I don't know
> > how to proceed for the construction of the model matrix.
> >
> > By using the suggestions of the "Direct Two Color Designs" example (chapter 7.4 LIMMA guide)
> > I did:
> >
> >
> >> targets
> > FileName Cy3 Cy5 Collection_time
> > 1 3_Myc24CD3gr_Myc24PBSre Myc_CD3 Myc_PBS 24h
> > 2 9_Myc24PBSgr_Myc24CD3re Myc_PBS Myc_CD3 24h
> > 3 5_Rag24CD3gr_Rag24PBSre Rag_CD3 Rag_PBS 24h
> > 4 4_Rag24PBSgr_Rag24CD3re Rag_PBS Rag_CD3 24h
> >
> >> designmyc= modelMatrix(targets, ref="Myc_PBS")
> > Found unique target names:
> > Myc_CD3 Myc_PBS Rag_CD3 Rag_PBS
> >
> >> designmyc
> > Myc_CD3 Rag_CD3 Rag_PBS
> > [1,] -1 0 0
> > [2,] 1 0 0
> > [3,] 0 -1 1
> > [4,] 0 1 -1
> >
> >> fit = lmFit(MA.Rq, designmyc)
> > Coefficients not estimable: Rag_PBS
> > Warning message:
> > Partial NA coefficients for 45018 probe(s)
> >
> >
> > But at this point I calculated just the ratios of Myc_CD3/Myc_PBS
> > and Rag_Myc/Myc_PBS (I am not really interested in this last one!).
> > How can I specify in the model matrix design that I need two different references
> > to calculate the following logratios: Myc_CD3/Myc_PBS, Rag_Myc/Rag_PBS?
> >
> >
> > Thank you in advance!
> > Giusy
> >
> >
> > _______________________________________________
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