[Frontiers in Bioscience E2, 171-186, January 1, 2010]

Cross phenotype normalization of microarray data

Jianhua Xuan1, Yue Wang1, Eric Hoffman2, Robert Clarke3

1Department of Electrical and Computer Engineering, Virginia Polytechnic Institute and State University, Arlington, VA 22203, USA, 2Research Center for Genetic Medicine, Children's National Medical Center, Washington, DC 20010, USA, 3Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20007, USA

TABLE OF CONTENTS

1. Abstract
2. Introduction
3. Normalization methods
3.1. Linear regression
3.2. Loess regression
3.3. Iterative ranking
3.4. Iterative nonlinear regression
4. Experimental results
4.1. Data sets and expression measurement
4.2 . Normalization plots
4.3. Performance comparison
4.3.1. Variance comparison
4.3.2. Fold-change comparison
5. Conclusion
6. Acknowledgments
7. References

1. ABSTRACT

Normalization is a prerequisite for almost all follow-up steps in microarray data analysis. Accurate normalization across different experiments and phenotypes assures a common base for comparative yet quantitative studies using gene expression data. In this paper, we report a comparison study of four normalization approaches, namely, linear regression (LR), Loess regression, invariant ranking (IR) and iterative nonlinear regression (INR) method, for gene expression. Among these four methods, LR and Loess regression methods use all available genes to estimate either a linear or nonlinear normalization function; while IR and INR methods feature some iterative processes to identify invariantly expressed genes (IEGs) for nonlinear normalization. We tested these normalization approaches on three real microarray data sets and evaluated their performance in terms of variance reduction and fold-change preservation. By comparison, we found that (1) LR method exhibits the worst performance in both variance reduction and fold-change preservation, and (2) INR method shows an improved performance in achieving low expression variance across replicates and excellent fold-change preservation for differently expressed genes.