A metabolic network model provides a computational framework for studying the metabolism of a cell at the system level. The organization of metabolic networks has been investigated in different studies. One of the organization aspects considered in these studies is the decomposition of a metabolic network. The decompositions produced by different methods are very different and there is no comprehensive evaluation framework to compare the results with each other. In this study, these methods are reviewed and compared in the first place. Then they are applied to six different metabolic network models and the results are evaluated and compared based on two existing and two newly proposed criteria. Results show that no single method can beat others in all criteria but it seems that the methods introduced by Guimera and Amaral and Verwoerd do better on among metabolite-based methods and the method introduced by Sridharan et al. does better among reaction-based ones. Also, the methods are applied to several artificial networks, each constructed from merging a few KEGG pathways. Then, their capability to recover those pathways are compared. Results show that among metabolite-based methods, the method of Guimera and Amaral does better again, however, no notable difference between the performances of reaction-based methods was detected.
Inferring gene regulatory networks (GRNs) is a challenging task in Bioinformatics. In this paper, an algorithm, PCHMS, is introduced to infer GRNs. This method applies the path consistency (PC) algorithm based on conditional mutual information test (PCA-CMI). In the PC-based algorithms the separator set is determined to detect the dependency between variables. The PCHMS algorithm attempts to select the set in the smart way. For this purpose, the edges of resulted skeleton are directed based on PC algorithm direction rule and mutual information test (MIT) score. Then the separator set is selected according to the directed network by considering a suitable sequential order of genes. The effectiveness of this method is benchmarked through several networks from the DREAM challenge and the widely used SOS DNA repair network of Escherichia coli. Results show that applying the PCHMS algorithm improves the precision of learning the structure of the GRNs in comparison with current popular approaches.
A metabolic network model provides a computational framework to study the metabolism of a cell at the system level. Due to their large sizes and complexity, rational decomposition of these networks into subsystems is a strategy to obtain better insight into the metabolic functions. Additionally, decomposing metabolic networks paves the way to use computational methods that will be otherwise very slow when run on the original genome-scale network. In the present study, we propose FCDECOMP decomposition method based on flux coupling relations (FCRs) between pairs of reaction fluxes. This approach utilizes a genetic algorithm (GA) to obtain subsystems that can be analyzed in isolation, i.e. without considering the reactions of the original network in the analysis. Therefore, we propose that our method is useful for discovering biologically meaningful modules in metabolic networks. As a case study, we show that when this method is applied to the metabolic networks of barley seeds and yeast, the modules are in good agreement with the biological compartments of these networks.
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