choosing normalization method for RNA-seq analysis
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@biase-fernando-4475
Last seen 9.6 years ago
Hi Working with edgeR package to analyze RNA-seq data, we have three options of normalization within calcNormFactors() function. Is there a way to test which one is more suitable for the data? If there is no test, is there a criteria to choose one over the other? Thanks in advance, Fernando
Normalization edgeR Normalization edgeR • 1.2k views
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@wolfgang-huber-3550
Last seen 16 days ago
EMBL European Molecular Biology Laborat…
Fernando, does it matter? I.e., for your data, do you get substantially different results from the different methods? If so, that might indicate a weakness of the data quality or of the experimental design that you would need to investigate in a manner specific to the dataset. Unsurprisingly, my personal favorite is "RLE". Wolfgang Biase, Fernando scripsit 17/03/11 22:53: > Hi > > Working with edgeR package to analyze RNA-seq data, we have three > options of normalization within calcNormFactors() function. Is there > a way to test which one is more suitable for the data? If there is no > test, is there a criteria to choose one over the other? > > Thanks in advance, Fernando > > _______________________________________________ Bioconductor mailing > list Bioconductor at r-project.org > https://stat.ethz.ch/mailman/listinfo/bioconductor Search the > archives: > http://news.gmane.org/gmane.science.biology.informatics.conductor -- Wolfgang Huber EMBL http://www.embl.de/research/units/genome_biology/huber
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Hi Dr. Huber, I believe you are correct in terms of the weakness of the experimental design. Unfortunately, I could not change it. I have 9 biological replicates sequenced for one group and 5 for another. Is there a down side of using DEseq to compare conditions with unbalanced sample number? One can argue that choosing either one of the normalization factors does not matter because I have about 85% of concordance of the results, but others can easily argue that it matters because of the difference on the results. And to add to the discrepancy on the results, when I analyze the data using one or the other normalization factor, there is a shift on the number of up regulated genes. For example: Genes Up in A genes Up in B RLM 2953 3322 TMM 3114 2632 I think it may easily affect the biological interpretation. I appreciated your reply, Thanks, Fernando -----Original Message----- From: bioconductor-bounces@r-project.org [mailto:bioconductor- bounces@r-project.org] On Behalf Of Wolfgang Huber Sent: Saturday, March 19, 2011 5:21 AM To: bioconductor at r-project.org Subject: Re: [BioC] choosing normalization method for RNA-seq analysis Fernando, does it matter? I.e., for your data, do you get substantially different results from the different methods? If so, that might indicate a weakness of the data quality or of the experimental design that you would need to investigate in a manner specific to the dataset. Unsurprisingly, my personal favorite is "RLE". Wolfgang Biase, Fernando scripsit 17/03/11 22:53: > Hi > > Working with edgeR package to analyze RNA-seq data, we have three > options of normalization within calcNormFactors() function. Is there a > way to test which one is more suitable for the data? If there is no > test, is there a criteria to choose one over the other? > > Thanks in advance, Fernando > > _______________________________________________ Bioconductor mailing > list Bioconductor at r-project.org > https://stat.ethz.ch/mailman/listinfo/bioconductor Search the > archives: > http://news.gmane.org/gmane.science.biology.informatics.conductor -- Wolfgang Huber EMBL http://www.embl.de/research/units/genome_biology/huber _______________________________________________ Bioconductor mailing list Bioconductor at r-project.org https://stat.ethz.ch/mailman/listinfo/bioconductor Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor
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