pipeLIMMA.voomfit<-function(counts, info, design, use.qualityWeights=TRUE, block, tests="all",geneIDs=NA, useBlock=TRUE, getTopTable=TRUE, getEbayes=T, contrasts=NULL, ...){
if(is.na(geneIDs)){
geneIDs<-rownames(counts)
}
y <- DGEList(counts = counts)
y <- calcNormFactors(y)
if(use.qualityWeights){
v <- voomWithQualityWeights(y, design=design, plot = F)
}else{
v <- voom(y, design=design, plot = F)
}
if(useBlock){
dupcor <- duplicateCorrelation(counts,design, block=as.factor(block))
fit <- lmFit(v, design=design, correlation=dupcor$consensus, block=as.factor(block))
}else{
fit <- lmFit(v, design=design)
}
efit<-eBayes(fit)
return(list(normFactors=y, voom=v, lmFit=fit, ebayes=efit))
}
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