Linear methods for analysis and quality control of relative expression ratios from quantitative real-time polymerase chain reaction experiments

Authors

Robert B. Page, College of Saint Benedict/Saint John's UniversityFollow
Arnold J. Stromberg

Document Type

Article

Publication Date

2011

Disciplines

Bioinformatics | Biotechnology | Computational Biology | Genetics

Abstract

Relative expression quantitative real-time polymerase chain reaction (RT-qPCR) experiments are a common means of estimating transcript abundances across biological groups and experimental treatments. One of the most frequently used expression measures that results from such experiments is the relative expression ratio (R_E), which describes expression in experimental samples (i.e., RNA isolated from organisms, tissues, and/or cells that were exposed to one or more experimental or nonbaseline condition) in terms of fold change relative to calibrator samples (i.e., RNA isolated from organisms, tissues, and/or cells that were exposed to a control or baseline condition). Over the past decade, several models of R_E have been proposed, and it is now clear that endogenous reference gene stability and amplification efficiency must be assessed in order to ensure that estimates of R_E are valid. In this review, we summarize key issues associated with estimating R_E from cycle threshold data. In addition, we describe several methods based on linear modeling that enable researchers to estimate model parameters and conduct quality control procedures that assess whether model assumptions have been violated.

Comments

DOI: 10.1100/tsw.2011.124

Recommended Citation

Page RB, Stromberg AJ. 2011. Linear methods for analysis and quality control of relative expression ratios from quantitative real-time polymerase chain reaction experiments. TheScientificWorldJournal 11:1383-1393.