rma or svn?
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@gjamdaimiaudk-642
Last seen 10.3 years ago
Hi, I'm using affimetrix chip data. I just heard of svn. Can anyone tell me the significant differences or improvement between rma and svn (and articles related to the answer if possible)? Thanks a lot, Jamila
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@rafael-a-irizarry-205
Last seen 10.3 years ago
first note vsn and rma are not competing methods. vsn is a normalization procedures, rma is a pre-preprocessing algorithm. the default normnalization for rma is quantile normalization. changing this to vsn works similarly. correlations for log expressions are higher than .9 the advantage of vsn over quantiles is that it, as the name states, stabilizes the variance, i.e. it removes the dependence of the variance on the total intensity. this gives genes with higher intensities an equal chace of being ranked high as genes with lower intensity. rma sometimes exhibits a slight dependence. two advantages of quantiels is that the implemented algorithm is faster and that you use a log tranformation of the data which is more interpretable than the arcsine (what vsn uses): log(a/b) is the log of fold change, but what is k1*arcsin(a)-k2*arcsin(b)? however, if all you care about is ranking of genes interpretability may not be as important. you can see "bottom-line" comparisons by looking at http://affycomp.biostat.jhsph.edu. the key entries to compare are 1) vsn to rma/nbg (entries 7,9) ---- without background subtraction 2) rma to rmavsn (entries 2 and 8) ---- with background subtraction here are some references: VSN ---- Parameter estimation for the calibration and variance stabilization of microarray data. W. Huber, A. von Heydebreck, H. Sltmann, A. Poustka, M. Vingron. Statistical Applications in Genetics and Molecular Biology (2003) Vol. 2: No. 1, Article 3 (See also: http://www.bepress.com/sagmb/vol2/iss1/art3) Variance stabilization applied to microarray data calibration and to the quantification of differential expression. W. Huber, A. von Heydebreck, H. Sltmann, A. Poustka, M. Vingron. Bioinformatics 18 suppl. 1 (2002), S96-S104 (ISMB 2002). QUANTILE NORMALIZATION ---------------------- Bolstad, B (2001) Probe Level Quantile Normalization of High Density Oligonucleotide Array Data http://www.stat.berkeley.edu/users/bolstad/stuff/qnorm.pdf Bolstad, B.M., Irizarry RA, Astrand, M, and Speed, TP (2003), A Comparison of Normalization Methods for High Density Oligonucleotide Array Data Based on Bias and Variance Bioinformatics. 19(2):185-193. RMA --- Irizarry, RA, Bolstad BM, Collin, F, Cope, LM, Hobbs, B, and, Speed, TP (2003) Summaries of Affymetrix GeneChip Probe Level Data. Nucleic Acids Research. Vol. 31, No. 4 e15 Irizarry, RA, Hobbs, B, Collin, F, Beazer-Barclay, YD, Antonellis, KJ, Scherf, U, Speed, TP (2003) Exploration, Normalization, and Summaries of High Density Oligonucleotide Array Probe Level Data. Biostatistics. Vol. 4, Number 2: 249-264. BENCHMARKS ----------- Cope, LM, Irizarry, RA, Jaffee, H, Wu, Z, Speed, TP (2003) A Benchmark for Affymetrix GeneChip Expression Measures. Bioinformatics 20: 323-331. > > Hi, > I'm using affimetrix chip data. I just heard of svn. Can anyone tell me the > significant differences or improvement between rma and svn (and articles > related to the answer if possible)? > > Thanks a lot, > Jamila > > _______________________________________________ > Bioconductor mailing list > Bioconductor@stat.math.ethz.ch > https://www.stat.math.ethz.ch/mailman/listinfo/bioconductor >
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