how to read in affy snp 500K arrays
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affy snp ▴ 640
@affy-snp-2480
Last seen 9.7 years ago
Dear list, I am analyzing a bag of Affy SNP 500K arrays and would like to know which package can be used to read in the raw .CEL files and get the intensity values. In other words, I am looking for the function like: library(affy) mydata <- ReadAffy() eset_rma <- rma(mydata) provided by affy package to analyze affy gene expression data. Thank you very much! Sincerely, Allen
SNP affy SNP affy • 1.1k views
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@benilton-carvalho-1375
Last seen 4.1 years ago
Brazil/Campinas/UNICAMP
check the oligo package, but you also need to download the data packages for the arrays you're using: pd.mapping250k.sty pd.mapping250k.nsp b On Nov 8, 2007, at 9:34 PM, affy snp wrote: > Dear list, > > I am analyzing a bag of Affy SNP 500K arrays and would like to > know which package can be used to read in the raw .CEL files > and get the intensity values. In other words, I am looking for > the function like: > > library(affy) > mydata <- ReadAffy() > eset_rma <- rma(mydata) > > provided by affy package to analyze affy gene expression data. > > Thank you very much! > > Sincerely, > Allen > > _______________________________________________ > Bioconductor mailing list > Bioconductor at stat.math.ethz.ch > https://stat.ethz.ch/mailman/listinfo/bioconductor > Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor
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Hi Benilton, Thanks for the note. What I intended to do is to get the intensity data from Affy SNP cel files and do copy number analysis. So for oligo, after snprma(), I can take the ave of the two strand and then accomplish what I said in the above? Best, Allen On Nov 9, 2007 11:29 PM, Benilton Carvalho <bcarvalh at="" jhsph.edu=""> wrote: > oligo doesn't "produce" data on both strands, per se. :-) > > The data are given on both strands, for some SNPs on the 500K array > set. If one uses snprma(), oligo *summarizes* these data to the > SNP-allele-strand level. > > It's a little bit hard to say what to do, when we don't know what it's > going to be used for... > > An ad-hoc method for summarization to the SNP-Allele level can be > achieved by taking the average log-intensities across strands; or one > can choose to manually run a summarization algorithm (say > median-polish) on the SNP-allele sets (a la RLMM). > > Cheers, > > b > > > On Nov 8, 2007, at 9:51 PM, affy snp wrote: > > > Hi Ben, > > > > I checked it out and found oligo would produce data for two strands, > > sense and anti-sense. > > Is there a way to somehow combine the two type of datawhich will make > > sense? > > > > Thank-you! > > > > Allen > > > > > > On 11/8/07, Benilton Carvalho <bcarvalh at="" jhsph.edu=""> wrote: check the > > oligo package, but you also need to download the data > >> packages for the arrays you're using: > >> > >> pd.mapping250k.sty > >> pd.mapping250k.nsp > >> > >> b > >> > >> On Nov 8, 2007, at 9:34 PM, affy snp wrote: > >> > >> > Dear list, > >> > > >> > I am analyzing a bag of Affy SNP 500K arrays and would like to > >> > know which package can be used to read in the raw .CEL files > >> > and get the intensity values. In other words, I am looking for > >> > the function like: > >> > > >> > library(affy) > >> > mydata <- ReadAffy() > >> > eset_rma <- rma(mydata) > >> > > >> > provided by affy package to analyze affy gene expression data. > >> > > >> > Thank you very much! > >> > > >> > Sincerely, > >> > Allen >
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