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PMID: 17720982 Published · ppublish English Comparative Study Evaluation Study Journal Article

A comparison of background correction methods for two-colour microarrays.

Bioinformatics (Oxford, England) ·Vol. 23 ·No. 20 ·2007-10-15 ·Pages 2700-7

Ritchie ME, Silver J, Oshlack A, Holmes M, Diyagama D, Holloway A, Smyth GK

Abstract

Microarray data must be background corrected to remove the effects of non-specific binding or spatial heterogeneity across the array, but this practice typically causes other problems such as negative corrected intensities and high variability of low intensity log-ratios. Different estimators of background, and various model-based processing methods, are compared in this study in search of the best option for differential expression analyses of small microarray experiments. Using data where some independent truth in gene expression is known, eight different background correction alternatives are compared, in terms of precision and bias of the resulting gene expression measures, and in terms of their ability to detect differentially expressed genes as judged by two popular algorithms, SAM and limma eBayes. A new background processing method (normexp) is introduced which is based on a convolution model. The model-based correction methods are shown to be markedly superior to the usual practice of subtracting local background estimates. Methods which stabilize the variances of the log-ratios along the intensity range perform the best. The normexp+offset method is found to give the lowest false discovery rate overall, followed by morph and vsn. Like vsn, normexp is applicable to most types of two-colour microarray data. The background correction methods compared in this article are available in the R package limma (Smyth, 2005) from http://www.bioconductor.org. Supplementary data are available from http://bioinf.wehi.edu.au/resources/webReferences.html.

MeSH Terms
Artifacts Image Enhancement/methods Image Interpretation, Computer-Assisted/methods In Situ Hybridization, Fluorescence/methods Microscopy, Fluorescence, Multiphoton/methods Oligonucleotide Array Sequence Analysis/methods Reproducibility of Results Sensitivity and Specificity
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Ritchie Matthew E
Department of Oncology, University of Cambridge, CRUK Cambridge Research Institute, Li Ka Shing Centre, Robinson Way, Cambridge CB2 0RE, UK.
Silver Jeremy
Oshlack Alicia
Holmes Melissa
Diyagama Dileepa
Holloway Andrew
Smyth Gordon K
Article Info
Journal
Bioinformatics (Oxford, England)
Abbr.
Bioinformatics
ISSN
1367-4811
Published
2007-10-15
Epub
2007-00-25
Pages
2700-7
Language
English
Region
England
NLM ID
9808944
Subset
IM
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