[BioC] two color arrays normalization
Giusy Della Gatta
Gatta at icg.cpmc.columbia.edu
Wed Feb 18 00:07:46 CET 2009
Hi Naomi,
I performed the analysis of my micorarrays,but still I don't manage to revert the channels!
My experiment consisted into infect cells with an adenovirus: an emty one
and an adenovirus expressing for a specific protein. Then I
treated the same cells with a specific drug or simply with the vehicle (DMSO).
I have 6 microarrays: 3 controls DMSO0-treated and 3 samples drug-treated.
In each microarray the green channel is expressing the levels of infected and treated
cells while the red channel are not infected cells. For all the experiments
I have the same RED CHANNEL reference.
I composed the target file as follows:
Filename Cy3 Cy5
Control_1b.txt ctrl ref
Control_2b.txt ctrl ref
Control_3b.txt ctrl ref
dexa_dbz_lt_1.txt treat ref
dexa_dbz_lt_2.txt treat ref
dexa_dbz_lt_3.txt treat ref
and the I used the following script:
>targets=readTargets("target_frame_ltbarc_pgedit.giusy")
>RG<-read.maimages(targets$FileName, source="agilent", ext="txt")
>MA<-MA.RG(RG, bc.method="normexp")
>MA<-normalizeWithinArrays(RG, method="loess")
>design <- modelMatrix(targets, ref="ref")
> design
ctrl treat
[1,] -1 0
[2,] -1 0
[3,] -1 0
[4,] 0 -1
[5,] 0 -1
[6,] 0 -1
>fit<-lmFit(MA,design)
>cont.matrix<-cbind("ctrl-ref"=c(1,0), "treat-ref"=c(0,1))
>cont.matrix
ctrl-ref treat-ref
[1,] 1 0
[2,] 0 1
>fit2<-contrasts.fit(fit, cont.matrix)
>d1 <- ebayes(fit2)
>toptable(fit2,adjust="fdr")
I don't know if I am still omitting
something, because I have the positive
controls of this experiment that
are going exactly in the opposite way!!
May you can help me?
Thank you in advance!
Giusy
-----Original Message-----
From: Naomi Altman [mailto:naomi at stat.psu.edu]
Sent: Mon 2/9/2009 9:56 PM
To: Giusy Della Gatta; bioconductor at stat.math.ethz.ch
Subject: Re: [BioC] two color arrays normalization
If there is no dye-swap, then what do you mean by "swapping of the colors"?
--Naomi
At 07:56 PM 2/9/2009, Giusy Della Gatta wrote:
>Hi everybody,
>
>I am analyzing two color Agilent microarrays
>by using LIMMA package.
>In my specific case the red channel is representing
>"the reference" while the green channel is "the treatment".
>Is it enough to use the Target File composition to specify the name
>of the samples
>and their corrispondet channels? Or I have to use other specific commands
>to specify the "swapping" of the colors?
>
>Thank you in advance!
>Regards
>Giusy
>
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Naomi S. Altman 814-865-3791 (voice)
Associate Professor
Dept. of Statistics 814-863-7114 (fax)
Penn State University 814-865-1348 (Statistics)
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