illumina normalisation using beadarray package
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@yogi-sundaravadanam-2312
Last seen 9.7 years ago
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Matt Ritchie ▴ 460
@matt-ritchie-2048
Last seen 9.7 years ago
Dear Yogi, We haven't looked in any detail at the effect different normalisations have on Illumina expression data. There are a few published studies which choose quantile normalisation (see reference list below) and this is the approach we often apply. You may also want to log2 transform your data before normalising it, i.e. BSData.quantile = normaliseIllumina(BSData, method = "quantile", transform="log2") Of course, it is always advisable to check that quantile is sensible for the data you're analysing with density plots etc. Best wishes, Matt ********* Papers which use quantile normalisation in the analysis of Illumina expression data: Elvidge GP, Glenny L, Appelhoff RJ, Ratcliffe PJ et al. Concordant regulation of gene expression by hypoxia and 2-oxoglutarate-dependent dioxygenase inhibition: the role of HIF-1alpha, HIF-2alpha, and other pathways. J Biol Chem 2006 Jun 2;281(22):15215-26. PMID: 16565084 Golubkov VS, Chekanov AV, Savinov AY, Rozanov DV et al. Membrane type-1 matrix metalloproteinase confers aneuploidy and tumorigenicity on mammary epithelial cells. Cancer Res 2006 Nov 1;66(21):10460-5. PMID: 17079467 Barnes M, Freudenberg J, Thompson S, Aronow B, Pavlidis P. Experimental comparison and cross-validation of the Affymetrix and Illumina gene expression analysis platforms. Nucleic Acids Res. 2005 Oct 19;33(18):5914-23. PMID: 16237126 > Hi all > > > > I?m quite new to illumina analysis. I read non-normalised data and did a > quantile normalisation. > > library(beadarray) > > BSData <- readBeadSummaryData(targets=NULL, header=T, sep="\t",path= > NULL, > > columns = list(ProbeID = "TargetID", > > AvgSig = "AVG_Signal", Nobeads = > "Avg_NBEADS", > > Detection="Detection", > BeadStDev="BEAD_STDEV"), > > other.columns = NULL, skip=7) > > BSData.quantile = normaliseIllumina(BSData, method = "quantile") > > normalised <- exprs(BSData.quantile) > > write.csv(file="normalised.csv", normalised) > > > > Is quantile normalisation good enough? What normalisation methods are > considered good for illumina data? Your feedback will be much > appreciated. > > > > Thanks heaps > > Yogi
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