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Open AccessJournal ArticleDOI

A comparison of background correction methods for two-colour microarrays

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TLDR
The model-based correction methods are shown to be markedly superior to the usual practice of subtracting local background estimates, and methods which stabilize the variances of the log-ratios along the intensity range perform the best.
Abstract
Motivation: 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. Results: 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. Availability: The background correction methods compared in this article are available in the R package limma (Smyth, 2005) from http://www.bioconductor.org. Contact: smyth@wehi.edu.au Supplementary information: Supplementary data are available from http://bioinf.wehi.edu.au/resources/webReferences.html.

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limma powers differential expression analyses for RNA-sequencing and microarray studies

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limma: Linear Models for Microarray Data

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References
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Journal ArticleDOI

Significance analysis of microarrays applied to the ionizing radiation response

TL;DR: A method that assigns a score to each gene on the basis of change in gene expression relative to the standard deviation of repeated measurements is described, suggesting that this repair pathway for UV-damaged DNA might play a previously unrecognized role in repairing DNA damaged by ionizing radiation.
Journal ArticleDOI

Linear Models and Empirical Bayes Methods for Assessing Differential Expression in Microarray Experiments

TL;DR: The hierarchical model of Lonnstedt and Speed (2002) is developed into a practical approach for general microarray experiments with arbitrary numbers of treatments and RNA samples and the moderated t-statistic is shown to follow a t-distribution with augmented degrees of freedom.
Journal ArticleDOI

Exploration, normalization, and summaries of high density oligonucleotide array probe level data

TL;DR: There is no obvious downside to using RMA and attaching a standard error (SE) to this quantity using a linear model which removes probe-specific affinities, and the exploratory data analyses of the probe level data motivate a new summary measure that is a robust multi-array average (RMA) of background-adjusted, normalized, and log-transformed PM values.
Book ChapterDOI

limma: Linear Models for Microarray Data

TL;DR: This chapter starts with the simplest replicated designs and progresses through experiments with two or more groups, direct designs, factorial designs and time course experiments with technical as well as biological replication.
Book

Bioinformatics and Computational Biology Solutions Using R and Bioconductor

TL;DR: In this article, the authors present a detailed case study of R algorithms with publicly available data, and a major section of the book is devoted to fully worked case studies, with a companion website where readers can reproduce every number, figure and table on their own computers.
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