Impact of normalization on miRNA microarray expression profiling

  1. Sylvain Pradervand1,2,4,
  2. Johann Weber1,4,
  3. Jérôme Thomas1,
  4. Manuel Bueno1,
  5. Pratyaksha Wirapati2,
  6. Karine Lefort3,
  7. G. Paolo Dotto3 and
  8. Keith Harshman1
  1. 1Lausanne DNA Array Facility, Center for Integrative Genomics, University of Lausanne, CH-1015 Lausanne, Switzerland
  2. 2Bioinformatics Core Facility, Swiss Institute of Bioinformatics, CH-1015 Lausanne, Switzerland
  3. 3Department of Biochemistry, University of Lausanne, CH-1066 Epalinges, Switzerland
  1. 4 These authors contributed equally to this work.

Abstract

Profiling miRNA levels in cells with miRNA microarrays is becoming a widely used technique. Although normalization methods for mRNA gene expression arrays are well established, miRNA array normalization has so far not been investigated in detail. In this study we investigate the impact of normalization on data generated with the Agilent miRNA array platform. We have developed a method to select nonchanging miRNAs (invariants) and use them to compute linear regression normalization coefficients or variance stabilizing normalization (VSN) parameters. We compared the invariants normalization to normalization by scaling, quantile, and VSN with default parameters as well as to no normalization using samples with strong differential expression of miRNAs (heart–brain comparison) and samples where only a few miRNAs are affected (by p53 overexpression in squamous carcinoma cells versus control). All normalization methods performed better than no normalization. Normalization procedures based on the set of invariants and quantile were the most robust over all experimental conditions tested. Our method of invariant selection and normalization is not limited to Agilent miRNA arrays and can be applied to other data sets including those from one color miRNA microarray platforms, focused gene expression arrays, and gene expression analysis using quantitative PCR.

Keywords:

Keywords

Footnotes

  • Reprint requests to: Sylvain Pradervand, Center for Integrative Genomics, University of Lausanne, 1015 Lausanne, Switzerland; e-mail: Sylvain.Pradervand{at}unil.ch; fax: 41-21-692-4065.

  • Article published online ahead of print. Article and publication date are at http://www.rnajournal.org/cgi/doi/10.1261/rna.1295509.

    • Received July 28, 2008.
    • Accepted December 5, 2008.
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