Displaying 3 results from an estimated 3 matches for "spikein".
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2007 Aug 06
1
Problems with expresso
Hello,
I want to use expresso for preprocessing the hgu133a-spikein data from
affycompII. But there is an error:
> library(affy)
> path <- "z:/Microarray/hgu133a-spikein/rawdata"
> celFile <- list.celfiles(path=path,full.names=TRUE);
> affyBatch <- ReadAffy(filenames=celFile[1:6]);
> eset1 <-
expresso(affyBatch,bgcorrect...
2010 Aug 04
1
error with ReadAffy()
Hi!I'm doing a little data importing from .cel files,
> setwd("/home/mandova/celfiles")
> mydata<-ReadAffy()
Error in sub("^/?([^/]*/)*", "", filenames, extended = TRUE) :
unused argument(s) (extended = TRUE)
Then I tried
> filenames<-paste("GSM",c(seq(138597,138617,1)),".cel",sep="")
>
2009 Mar 13
0
Singal channel spike in controls with custom microRNA slides - Normalization help needed
...My gpr files do only contain 1 channel (Cy5)
RG <- read.maimages(
targets$FileName,source="genepix",columns=list(R=Cy5,G=Cy5, Rb=Cy5b,
Gb=Cy5b))
RG$G <- NULL
RG$Gb <- NULL
RG$genes <- readGAL("array_human_mirs.gal")
#Here are my spike in controls for normalization
isSpikeIn <- grep("CTL", RG$genes$Name)
#The vsn normalization works fine
mat <- vsnMatrix(RG$R)
However i would like to normaliza using my spikein controls by block or by
using the mean of all controls.
Could you help on that ??
thanks,
david
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