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anupam sinha
▴
270
@anupam-sinha-3207
Last seen 10.3 years ago
Dear list,
I use the following code to process some cel files
I have
:
> dat<-ReadAffy()
> dat_norm<-rma(dat)
Background correcting
Normalizing
Calculating Expression
> dat_norm_mat<-exprs(dat_norm)
>
write.table(dat_norm_mat,"GSE3185.txt",sep="\t",row.names=T,col.names=
T,quote=F)
and I get the following output in the text file :
GSM48598.CEL GSM48599.CEL
GSM48600.CEL GSM48601.CEL GSM48602.CEL
100_g_at 3.47028618802937 3.49106274273872
3.46940719815954 3.46836687956259 3.45079245249753
.
.
.
I have couple of questions.
1) How do I add one more column to the text file which will give the
gene
symbol for each of the probe-id ?
2) Do the expression values get log2 transformed (after "rma"
normalization
is done on the cel files or I have to perform it separately) ?
This is my sessionInfo():
R version 2.10.0 (2009-10-26)
i386-redhat-linux-gnu
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=C LC_MESSAGES=en_US.UTF-8
[7] LC_PAPER=en_US.UTF-8 LC_NAME=C
[9] LC_ADDRESS=C LC_TELEPHONE=C
[11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
attached base packages:
[1] splines tcltk stats graphics grDevices datasets utils
[8] methods base
other attached packages:
[1] WGCNA_0.89 Hmisc_3.8-0 survival_2.35-7
[4] qvalue_1.22.0 flashClust_1.00 dynamicTreeCut_1.21
[7] impute_1.22.0 hgu95av2cdf_2.5.0 affy_1.24.2
[10] Biobase_2.6.1 limma_3.2.3 R.utils_1.4.0
[13] R.oo_1.7.2 R.methodsS3_1.2.0
loaded via a namespace (and not attached):
[1] affyio_1.14.0 cluster_1.12.1 grid_2.10.0
[4] lattice_0.17-26 preprocessCore_1.8.0 tools_2.10.0
Thanks in advance for any suggestions.
Regards,
Anupam
--
Graduate Student,
Center For DNA Fingerprinting And Diagnostics,
4-1-714 to 725/2, Tuljaguda complex
Mozamzahi Road, Nampally,
Hyderabad-500001
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