PGSEA Steps Using Bioconductor
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livdiehard • 0
@livdiehard-9794
Last seen 8.8 years ago

Hi

Am doing my final year project on a web base application for microarray .
One of my faeture is Gene Set Analysis using the PGSEA technique.
the problem is that am getting confusion with some of the codes.

For Gene Set Analysis, the user has to inputs:

1)CELL Files
2)choose identifier type
3)choose GO
4)choose the pgsea method.

What I actually do is determing in the code below where to pass the identifier and the GO?
Can you help me out?

####code

library(PGSEA)
library(GEOquery)
library(GSEABase)
library(hgu133plus2.db)
gse <- getGEO("GSE7023",GSEMatrix=TRUE)

subtype <- gsub("\\.", "_",gsub("subtype: ", "", phenoData(gse[[1]])$"characteristics_ch1"))
pheno <- new("AnnotatedDataFrame", data = data.frame(subtype), varMetadata = data.frame(labelDescription="subtype"))
rownames(pheno@data) <- colnames(exprs(gse[[1]]))
eset <- new("ExpressionSet", exprs = exprs(gse[[1]]), phenoData = pheno)

data(VAIgsc)
details(VAIgsc[[1]])

pg <- PGSEA(eset, VAIgsc, ref=which(subtype=="NO"))

pg[5:8, 5:8]

range(pg, finite=TRUE)
smcPlot(pg, col=.rwb, scale=c(-15, 15))

microarray pgsea • 1.1k views
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Entering edit mode

Edited your question to add the 'pgsea' tag. This makes it more likely that the maintainer of that package will see your question.

 

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