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A Bayesian mixture model for metaanalysis of microarray studies. | LitMetric

A Bayesian mixture model for metaanalysis of microarray studies.

Funct Integr Genomics

Department of Mathematics and Statistics, University of Massachusetts, 710 North Pleasant Street, Amherst, MA 01003-9305, USA.

Published: February 2008

AI Article Synopsis

  • Increased availability of microarray data necessitates improved statistical methods to integrate findings, particularly in identifying differentially expressed genes between conditions like treatment versus control.
  • A new Bayesian three-component truncated normal mixture model enhances differential expression analysis by categorizing genes into three groups: upregulated, downregulated, and nonexpressed, compared to the previous two-component model that only distinguished expressed and nonexpressed genes.
  • Simulations and biological data analysis showed that this three-component model outperformed the two-component model in identifying more significant genes while maintaining accuracy in posterior probabilities and reducing false discovery rates.

Article Abstract

The increased availability of microarray data has been calling for statistical methods to integrate findings across studies. A common goal of microarray analysis is to determine differentially expressed genes between two conditions, such as treatment vs control. A recent Bayesian metaanalysis model used a prior distribution for the mean log-expression ratios that was a mixture of two normal distributions. This model centered the prior distribution of differential expression at zero, and separated genes into two groups only: expressed and nonexpressed. Here, we introduce a Bayesian three-component truncated normal mixture prior model that more flexibly assigns prior distributions to the differentially expressed genes and produces three groups of genes: up and downregulated, and nonexpressed. We found in simulations of two and five studies that the three-component model outperformed the two-component model using three comparison measures. When analyzing biological data of Bacillus subtilis, we found that the three-component model discovered more genes and omitted fewer genes for the same levels of posterior probability of differential expression than the two-component model, and discovered more genes for fixed thresholds of Bayesian false discovery. We assumed that the data sets were produced from the same microarray platform and were prescaled.

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Source
http://dx.doi.org/10.1007/s10142-007-0058-3DOI Listing

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