[BioC] Methods to combine U133A and B?
Adaikalavan Ramasamy
ramasamy at cancer.org.uk
Thu Jul 15 20:11:04 CEST 2004
The easiest way is to prefix each probeset ID with A or B indicating
U133A and U133B. Suppose dataA and dataB represents your expression
values from U133A and U133B respectively, then
rownames(dataA) <- paste("A.", rownames(dataA), sep="")
rownames(dataB) <- paste("B.", rownames(dataB), sep="")
stopifnot( identical( colnames(dataA), colnames(dataB) ) )
newdata <- rbind( dataA, dataB )
write.table(newdata, file="output.txt", sep="\t", quote=FALSE)
If you are thinking about calibrating U133A results to U133B, then the
problem becomes more difficult. I asked a related question to this and
you can search for the mailing list archives for the keywords "combining
HGU133 chips".
Regards, Adai.
On Thu, 2004-07-15 at 17:41, Simon Lin wrote:
> Greetings,
>
> I have some samples measured by both U133A and U133B. Is there a way to
> combine results from these chips together into one result file? (i.e., take
> care of the replicated probe sets on both chips?)
>
> I took a look at the matchprobe package, but I think that is not exactly
> what I need.
>
> Thanks!
>
> Simon
>
> _______________________________________________
> Bioconductor mailing list
> Bioconductor at stat.math.ethz.ch
> https://www.stat.math.ethz.ch/mailman/listinfo/bioconductor
>
More information about the Bioconductor
mailing list