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  • aquila
    Junior Member
    • Dec 2010
    • 6

    Normalization: DESeq vs. EdgeR with method="RLE"

    Hello all,

    I am trying out different normalization methods for RNA-seq.
    The newest release of EdgeR offers (among others) a normalization method called "RLE" that is supposed to be an implementation of what is also implemented in DESeq. This is explained in the edgeR manual. See ?calcNormFactors.

    I thus expected to obtain the same normalization factors with both packages.
    I am using part of the MAQC-2 data set that is referenced in a number of papers on RNA-seq. There are 14 samples, of which 7 are brain and 7 are UHR.

    Here's what I tried:


    "countsMatrix" is a matrix of raw counts (one column for each sample)
    conds <- c( rep("brain", 7), rep("UHR", 7))

    a)
    cds <- newCountDataSet( countsMatrix, conds )
    cds <- estimateSizeFactors( cds )
    sizeFactors(cds)

    b)
    d <- DGEList(counts=countsMatrix, group=conds, lib.size=colSums(countsTable))
    d <- calcNormFactors(d, method="RLE")
    d$samples$norm.factors


    Results:
    a)
    1.1430 1.1597 1.1695 1.1707 1.1751 0.3293 1.1643 1.1489 1.1650 1.1781 1.1802 0.4877 1.1617 1.1596

    b)
    1.0546 1.0354 1.0167 1.0291 1.0178 0.7133 1.0330 1.0645 1.0705 1.0876 1.0837 0.7619 1.0796 1.0564


    Might anyone have a suggestion why the resulting normalization factors are different?
  • Jouneau Luc
    Junior Member
    • Apr 2011
    • 2

    #2
    Hello aquila,

    would you please tell me where did you download this MAQC dataset ?

    Thanks in advance

    Luc

    Comment

    • aquila
      Junior Member
      • Dec 2010
      • 6

      #3
      The data is available on


      Search for: SRA010153

      There are several data sets there. I downloaded the following:

      SRX016368 (7 samples)
      SRX016366 (7 samples)


      I found these data sets referenced in the following publication (among others):
      Bullard et al, Evaluation of statistical methods for normalization and differential expression in mRNA-Seq experiments, BMC Bioinformatics 2010, 11:94.

      Comment

      • ning
        Junior Member
        • Oct 2010
        • 4

        #4
        Hi aquila




        For edgeR, I guess you need to multiply the output of calcNormFactors() by the library size to get the "normalization factor"?

        Comment

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