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On the Choice and Number of Microarrays for Transcriptional Regulatory Network Inference

DOI: 10.1186/1471-2105-11-454

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Abstract:

We present evidence of substantial effective dependency among microarrays in this compendium, and characterize that dependency with respect to experimental condition factors. We then introduce a measure neff of the effective number of experiments in a compendium, and find that corresponding to the dependency observed in this particular compendium there is a huge reduction in effective sample size i.e., neff = 14.7 versus n = 376. Furthermore, we found that the neff of select subsets of experiments actually exceeded neff of the full compendium, suggesting that the adage 'less is more' applies here. Consistent with this latter result, we observed improved performance in TRNI using subsets of the data compared to results using the full compendium. We identified experimental condition factors that trend with changes in TRNI performance and neff , including growth phase and media type. Finally, using the set of known E. coli genetic regulatory interactions from RegulonDB, we demonstrated that false discovery rates (FDR) derived from neff -adjusted p-values were well-matched to FDR based on the RegulonDB truth set.These results support utilization of neff as a potent descriptor of microarray compendia. In addition, they highlight a straightforward correlation-based method for TRNI with demonstrated meaningful statistical testing for significant edges, readily applicable to compendia from any species, even when a truth set is not available. This work facilitates a more refined approach to construction and utilization of mRNA expression compendia in TRNI.With the availability of genome-wide mRNA expression data from DNA microarray experiments, transcriptional regulatory network inference (TRNI) from large compendia of these microarrays has become a fundamental task in computational systems biology. In this approach, transcription factor (TF)-gene interactions are predicted based on observed trends in mRNA expression across many experimental conditions. Unsupervised pairwise

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