Quality control and robust estimation for cDNA microarrays with replicates

• 成果类型: Article
• 署名作者: Gottardo, R; Raftery, AE; Yeung, KY; Bumgarner, RE
• 署名单位: University of British Columbia; University of Washington; University of Washington Seattle; University of Washington; University of Washington Seattle
• 刊物名称: JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION
• ISSN/ISSBN: 0162-1459
• DOI: 10.1198/016214505000001096
• 发表日期: 2006
• 页码: 30-40
• 关键词: differentially-expressed genes; statistical-analysis; image-analysis; variance; transformations; normalization; DESIGN

摘要

We consider robust estimation of gene intensities from cDNA microarray data with replicates. Several statistical methods for estimating gene intensities from microarrays have been proposed, but little work has been done on robust estimation. This is particularly relevant for experiments with replicates, because even one outlying replicate can have a disastrous effect on the estimated intensity for the gene concerned. Because of the many steps involved in the experimental process from hybridization to image analysis, cDNA microarray data often contain outliers. For example, an outlying data value could occur because of scratches or dust on the surface, imperfections in the glass, or imperfections in the array production. We develop a Bayesian hierarchical model for robust estimation of cDNA microarray intensities. Outliers are modeled explicitly using a t-distribution, and our model also addresses such classical issues as design effects, normalization, transformation, and nonconstant variance. Parameter estimation is carried out using Markov chain Monte Carlo. By identifying potential outliers, the method provides automatic quality control of replicate, array, and gene measurements. The method is applied to three publicly available gene expression datasets and compared with three other methods: ANOVA-normalized log ratios, the median log ratio, and estimation after the removal of outliers based on Dixon's test. We find that the between-replicate variability of the intensity estimates is lower for our method than for any of the others. We also address the issue of whether the background should be subtracted when estimating intensities. It has been argued that this should not be done because it increases variability, whereas the arguments for doing so are that there is a physical basis for the image background, and that not doing so will bias downward the estimated log ratios of differentially expressed genes. We show that the arguments on both sides of this debate are correct for our data, but that by using our model one can have the best of both worlds: One can subtract the background without increasing variability by much.