Abstract

BackgroundGene regulatory networks have an essential role in every process of life. In this regard, the amount of genome-wide time series data is becoming increasingly available, providing the opportunity to discover the time-delayed gene regulatory networks that govern the majority of these molecular processes.ResultsThis paper aims at reconstructing gene regulatory networks from multiple genome-wide microarray time series datasets. In this sense, a new model-free algorithm called GRNCOP2 (Gene Regulatory Network inference by Combinatorial OPtimization 2), which is a significant evolution of the GRNCOP algorithm, was developed using combinatorial optimization of gene profile classifiers. The method is capable of inferring potential time-delay relationships with any span of time between genes from various time series datasets given as input. The proposed algorithm was applied to time series data composed of twenty yeast genes that are highly relevant for the cell-cycle study, and the results were compared against several related approaches. The outcomes have shown that GRNCOP2 outperforms the contrasted methods in terms of the proposed metrics, and that the results are consistent with previous biological knowledge. Additionally, a genome-wide study on multiple publicly available time series data was performed. In this case, the experimentation has exhibited the soundness and scalability of the new method which inferred highly-related statistically-significant gene associations.ConclusionsA novel method for inferring time-delayed gene regulatory networks from genome-wide time series datasets is proposed in this paper. The method was carefully validated with several publicly available data sets. The results have demonstrated that the algorithm constitutes a usable model-free approach capable of predicting meaningful relationships between genes, revealing the time-trends of gene regulation.

Highlights

  • Gene regulatory networks have an essential role in every process of life

  • Regarding the regulatory network under study in this work that corresponds to the Saccharomyces cerevisiae organism, the CLB2 and SWI5 genes are shown to be potentially activated by CLB1 gene, but their respective upregulation thresholds are different

  • Thereby, we have introduced a parameter on the consensus process, called Rule Consensus Accuracy (RCA), which specifies the minimum proportion of datasets in which a rule must predict well in order to be returned by the algorithm as a potential relationship

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Summary

Introduction

Gene regulatory networks have an essential role in every process of life. In this regard, the amount of genome-wide time series data is becoming increasingly available, providing the opportunity to discover the timedelayed gene regulatory networks that govern the majority of these molecular processes. The genome encodes thousands of genes whose products enable cell survival and numerous cellular functions. The amount and the temporal pattern in which these products appear in the cell are crucial to the processes of life. Gene Regulatory Networks (GRNs) govern the levels of these gene products. Numerous cellular processes are affected by regulatory networks. Innovations in experimental methods have enabled large scale studies that allow parallel genome-wide gene expression measurements of the products of thousands

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