[BioC] M values
Sean Davis
sdavis2 at mail.nih.gov
Tue Sep 30 17:54:38 CEST 2008
On Tue, Sep 30, 2008 at 11:39 AM, Jose Francisco Rodriguez
<francquimico at gmail.com> wrote:
> Hi:
> Actually it worked using this command:
>
> write.csv(MA$M,file="Mvalues.csv")
>
> Is this OK?
>
> Thank You for your help!!!!
Glad to hear you got it working.
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Sean
> On Tue, Sep 30, 2008 at 11:29 AM, Sean Davis <sdavis2 at mail.nih.gov> wrote:
>>
>> On Tue, Sep 30, 2008 at 10:47 AM, Jose Francisco Rodriguez
>> <francquimico at gmail.com> wrote:
>> > Hi:
>> > Thank You! I applied this command (MA$M) and obtained the values, but
>> > I'm
>> > having problems creating an excel table for those. I suppose that I
>> > should
>> > use write.table, but I dont know how to put the command without giving
>> > me an
>> > error. Sorry but I'm still learning.
>>
>> What have you tried? And what error do you get?
>>
>> Sean
>>
>>
>> > On 9/30/08, Sean Davis <sdavis2 at mail.nih.gov> wrote:
>> >>
>> >> On Tue, Sep 30, 2008 at 9:42 AM, Jose Francisco Rodriguez
>> >> <francquimico at gmail.com> wrote:
>> >> > Hi:
>> >> > I performed a microarray (5 biological replicates) and analyzed using
>> >> > Limma. The software gives me the M value as a combination from the 5
>> >> > biological replicates microarray. In order to submit the data to GEO
>> >> > database we need the M-value for each array ( 5 M-values). How can I
>> >> > do
>> >> > that? I'll appreciate your help.
>> >>
>> >> MA$M contains the M values for each array.
>> >>
>> >> Sean
>> >>
>> >> > Below there is a copy of the sequence for the analysis:
>> >> >
>> >> > library(limma)
>> >> > library(geneplotter)
>> >> >
>> >> > ###Lee targets y image files
>> >> > targets=readTargets("maTargetFKS12.txt")
>> >> >
>> >> > RG=read.maimages(files=cbind(targets$FileNameCy3,targets$FileNameCy5),
>> >> > source="imagene")
>> >> >
>> >> > ##lear gal
>> >> > gal=readGAL("013384_D_20050601.gal")
>> >> > gal=gal[1:nrow(RG$R),]
>> >> > ##asignar el gal
>> >> > RG$genes=gal
>> >> >
>> >> > ###definir los Spot Types y colores
>> >> > spottypes <- readSpotTypes() ##usamos el default que es SpotTypes
>> >> > RG$genes$Status <- controlStatus(spottypes, RG)
>> >> >
>> >> > ###definir el layour
>> >> > printer= list(ngrid.r=1,ngrid.c=1,nspot.r=107,nspot.c=101)
>> >> > RG$printer=structure(printer, class = "PrintLayout")
>> >> >
>> >> > ###normalize: background y normlize within
>> >> > RGoriginal = RG
>> >> > RG <- backgroundCorrect(RGoriginal, method="normexp", offset=50)
>> >> > MA = normalizeWithinArrays(RG,method="loess",bc.method="none")
>> >> >
>> >> > ##escoger los genes nadamas
>> >> > geneIndex = which(MA$genes$Status=="gene")
>> >> >
>> >> > ##preparar el disenyo para fit
>> >> > design = modelMatrix(targets,ref="WT")
>> >> >
>> >> > ###ver todos los MA plots como QC: todos OK!
>> >> > for(i in 1:6){
>> >>
>> >> > >
>> >> > > plotMA(MA[geneIndex,i],main=targets$Name[i],ylim=range(MA$M[geneIndex,]))
>> >> > scan()
>> >> > }
>> >> >
>> >> > ###estimar los paramteros usando eBayes (moderated t-stat) y calcular
>> >> > FDR
>> >> > fit1 = lmFit(MA,design)
>> >> > fit1 = eBayes(fit1)
>> >> > tt=topTable(fit1,adjust="fdr",number=3000)
>> >> > tt=tt[tt$P.Value<=0.01,]
>> >> >
>> >> > ###Escoger genes para incluir en las graficas
>> >> > Index=as.numeric(rownames(tt))
>> >> > interestGenes <-
>> >> >
>> >> >
>> >> > c("CHS3","SLT2","PIR3","ECM4","ECM13","SPI1","ORF:YHR097C","MYO1","PIR3","HOG1","SWE1")
>> >> > interestIndex <- lapply(interestGenes,function(x)
>> >> > which(MA$genes$GeneName==x))
>> >> > names(interestIndex) <- interestGenes
>> >> >
>> >> > ##MA-PLOT
>> >> >
>> >> >
>> >> > plot(fit1$Amean[geneIndex],fit1$coef[geneIndex],pch=".",col="grey",ylab="M",xlab="A")
>> >> > points(fit1$Amean[Index],fit1$coef[Index],pch=16,col="blue",cex=.5)
>> >> > for(i in seq(along=interestGenes)){
>> >> >
>> >> >
>> >> >
>> >> > text(fit1$Amean[interestIndex[[i]]],fit1$coef[interestIndex[[i]]],interestGenes[i],cex=.5)
>> >> > }
>> >> >
>> >> > ##VOLCANO
>> >> >
>> >> >
>> >> > plot(fit1$coef[geneIndex],-log10(fit1$p.value[geneIndex]),pch=".",col="grey",xlab="M",ylab="-log_10
>> >> > p-value")
>> >> >
>> >> >
>> >> > points(fit1$coef[Index],-log10(fit1$p.value[Index]),pch=16,col="blue",cex=.5)
>> >> > for(i in seq(along=interestGenes)){
>> >> >
>> >> >
>> >> >
>> >> > text(fit1$coef[interestIndex[[i]]],-log10(fit1$p.value[interestIndex[[i]]]),interestGenes[i],cex=.5)
>> >> > }
>> >> >
>> >> >
>> >> > ###hacer xls file
>> >> > todos = topTable(fit1,adjust="fdr",number=10807)
>> >> > write.csv(todos,file="myo1.csv")
>> >> > --
>> >> > José F. Rodríguez Quiñones
>> >> > Graduate student
>> >> > School of Medicine
>> >> > Medical Sciences Campus
>> >> > University of Puerto Rico
>> >> >
>> >> > [[alternative HTML version deleted]]
>> >> >
>> >> >
>> >> > _______________________________________________
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>> >> >
>> >
>> >
>> >
>> > --
>> > José F. Rodríguez Quiñones
>> > Graduate student
>> > School of Medicine
>> > Medical Sciences Campus
>> > University of Puerto Rico
>
>
>
> --
> José F. Rodríguez Quiñones
> Graduate student
> School of Medicine
> Medical Sciences Campus
> University of Puerto Rico
>
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