[BioC] justRMA?
James W. MacDonald
jmacdon at uw.edu
Fri Dec 7 22:42:11 CET 2012
Hi Bargavi,
On 12/7/2012 4:08 PM, Bhargavi Duvvuri wrote:
> Hello,
>
> I am using justRMA for processing 350 CEL files. When I does with RMA I get
> 34901 probe intensities which match the CDF file. However, when I run
> justRMA, I get only 23068 probe intensities. I am not sure why would this
> happen?
It shouldn't, and we have done extensive testing to ensure that the
results from justRMA() are identical to rma(). As an example:
> nrow(exprs(rma(ReadAffy(cdfname = "mogene10stmmrefseqcdf"))))
Background correcting
Normalizing
Calculating Expression
[1] 28312
> nrow(exprs(justRMA(cdfname = "mogene10stmmrefseqcdf")))
[1] 28312
So I get the same number of rows using both methods. Now check that I
get the same exact values:
> all.equal(exprs(rma(ReadAffy(cdfname =
"mogene10stmmrefseqcdf"))),exprs(justRMA(cdfname =
"mogene10stmmrefseqcdf")))
Background correcting
Normalizing
Calculating Expression
[1] TRUE
So it looks OK to me.
Best,
Jim
> sessionInfo()
R version 2.15.1 (2012-06-22)
Platform: x86_64-unknown-linux-gnu (64-bit)
locale:
[1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
[3] LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8
[5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
[7] LC_PAPER=C LC_NAME=C
[9] LC_ADDRESS=C LC_TELEPHONE=C
[11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
attached base packages:
[1] stats graphics grDevices utils datasets methods base
other attached packages:
[1] mogene10stmmrefseqcdf_16.0.0 mogene11stmmrefseqcdf_16.0.0
[3] mogene10stv1cdf_2.11.0 AnnotationDbi_1.20.3
[5] affy_1.36.0 Biobase_2.18.0
[7] BiocGenerics_0.4.0
loaded via a namespace (and not attached):
[1] affyio_1.26.0 BiocInstaller_1.8.3 DBI_0.2-5
[4] IRanges_1.16.4 parallel_2.15.1 preprocessCore_1.20.0
[7] RSQLite_0.11.2 stats4_2.15.1 tools_2.15.1
[10] zlibbioc_1.4.0
>
>
> Below is the code I am using:
>
> library(affy)
> setwd('/home/run/testcel')
> expr.vals<- justRMA(cdfname = "primeviewhsrefseqcdf")
> write.exprs(expr.vals, file= 'Customoutput.csv', sep=",", row.names=F,
> col.names=T, quote=F)
>
> Could you please advise me here on how to modify the script so that I
> get normalized probe intensities for all the probe sets?
>
> Thank you for your attention and time.
>
> Bhargavi
>
> [[alternative HTML version deleted]]
>
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--
James W. MacDonald, M.S.
Biostatistician
University of Washington
Environmental and Occupational Health Sciences
4225 Roosevelt Way NE, # 100
Seattle WA 98105-6099
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