st 1.0 gene quality measures
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@richard-friedman-513
Last seen 9.6 years ago
Dear Bioconductor List, Is there a way to get quality measurements on ST 1.0 Gene Arrays analogous to the standard workup for mouse 430? That is to say plm functions (NUSE, signed resids etc). unnormlaizd boxplots and rma normlaized boxplots. pca , hist It is not clear to me how to do this from the documentation to the oligo pacakage. I would greatly appreciate any suggestions that you might have. Thanks and best wishes, Rich ------------------------------------------------------------ Richard A. Friedman, PhD Associate Research Scientist, Biomedical Informatics Shared Resource Herbert Irving Comprehensive Cancer Center (HICCC) Lecturer, Department of Biomedical Informatics (DBMI) Educational Coordinator, Center for Computational Biology and Bioinformatics (C2B2)/ National Center for Multiscale Analysis of Genomic Networks (MAGNet) Room 824 Irving Cancer Research Center Columbia University 1130 St. Nicholas Ave New York, NY 10032 (212)851-4765 (voice) friedman at cancercenter.columbia.edu http://cancercenter.columbia.edu/~friedman/ "Did he win the Nobel prize or the Ig Nobel prize for levitating the frog?". Rose Friedman, age 14
Cancer Cancer • 997 views
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Davis, Wade ▴ 350
@davis-wade-2803
Last seen 9.6 years ago
Hi Rich, Please check out the aroma.affymetrix package and their very helpful website here: http://www.aroma-project.org/ It is a very powerful package, and I think a little bit of overkill for ST arrays, but that is the only way I have found to get the plots you are looking for (not that I have looked that hard for other packages that could do it). When using the aroma.affymetrix package, you have to be very specific in how the data files (and folders) are named and structured, which is all documented on their web site. Once you do that, you can fit an RMA probe-level (PLM) model, and then do something like this: ################################################################# ### Quality assessment of PLM fit ################################################################# #To examine NUSE and RLE plots, do brca.qam <- QualityAssessmentModel(brca.plm) par(mfrow=c(1,2)) plotNuse(brca.qam) plotRle(brca.qam) If you want some additional QC plots, you can also use the affyQCReport package. It doesn't work entirely because some of its functions aren't defined for ST arrays (no mismatch probes), but you can get most of the plots that are generated by QCReport() using the following code (note this is for a different data set than used above). Getting the annotation correct is the only slightly tricky part. Here I was using Mouse ST 1.0 array. library(affy) library(geneplotter) library(simpleaffy) library(limma) library(statmod) library(lattice) library(mogene10sttranscriptcluster.db) MEF.eSet <- ReadAffy(phenoData=read.AnnotatedDataFrame(filename="sampl e_info.csv",sep = ",")) annotation(MEF.eSet) = "mogene10sttranscriptcluster.db" ################################################### ### Quality Control ################################################### #Used Aroma.affymetrix for NUSE and RLE plot, they looked fine. #affyQC Report doesn't work well with ST arrays library(affyQCReport) #QCReport(MEF.eSet,file="MEF_PreProc_QC2.pdf") ## Read this entire thread about QCReport and ST ##http://thread.gmane.org/gmane.science.biology.informatics.conductor/ 32460/focus=32815 #However, this does everything but the degradation plot pdf("myownQC.pdf") borderQC1(MEF.eSet) borderQC2(MEF.eSet) correlationPlot(MEF.eSet) titlePage(MEF.eSet) signalDist(MEF.eSet) MEF.norm <- expresso(MEF.eSet, bgcorrect.method="rma", normalize.method="quantiles",#normalize.method="qspline", pmcorrect.method="pmonly", summary.method="medianpolish") library(affycoretools) #par(mfrow=c(2,1)) plotHist(MEF.eSet) # prior to any normalization, etc plotDeg(MEF.eSet) dev.off() HTH, Wade J. Wade Davis, PhD Assistant Professor 187 Galena DC 018.0 University of Missouri Columbia, MO 65212 Phone: (573) 882-0770 Fax: (573) 884-4196 MU Biostatistics Group -----Original Message----- From: Richard Friedman [mailto:friedman@cancercenter.columbia.edu] Sent: Thursday, February 03, 2011 5:46 PM To: Bioconductor mailing list Subject: [BioC] st 1.0 gene quality measures Dear Bioconductor List, Is there a way to get quality measurements on ST 1.0 Gene Arrays analogous to the standard workup for mouse 430? That is to say plm functions (NUSE, signed resids etc). unnormlaizd boxplots and rma normlaized boxplots. pca , hist It is not clear to me how to do this from the documentation to the oligo pacakage. I would greatly appreciate any suggestions that you might have. Thanks and best wishes, Rich ------------------------------------------------------------ Richard A. Friedman, PhD Associate Research Scientist, Biomedical Informatics Shared Resource Herbert Irving Comprehensive Cancer Center (HICCC) Lecturer, Department of Biomedical Informatics (DBMI) Educational Coordinator, Center for Computational Biology and Bioinformatics (C2B2)/ National Center for Multiscale Analysis of Genomic Networks (MAGNet) Room 824 Irving Cancer Research Center Columbia University 1130 St. Nicholas Ave New York, NY 10032 (212)851-4765 (voice) friedman@cancercenter.columbia.edu http://cancercenter.columbia.edu/~friedman/ "Did he win the Nobel prize or the Ig Nobel prize for levitating the frog?". Rose Friedman, age 14 [[alternative HTML version deleted]]
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