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Module detection for bacteria based on spectral clustering of protein-protein functional association networks

机译:基于蛋白质-蛋白质功能关联网络光谱聚类的细菌模块检测

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Network analysis-based module detection has significant implications in many fields. In cellular/ molecular biology, module detection based on analyses of metabolic/regulatory networks will not only help us understand more about the function and evolution of cellular machinery of an organism, but will also provide tractable contextual information for potential drug targets and facilitate improvements in drug designs. We here present our preliminary study on the module detection for bacteria based on the spectral clustering of the protein-protein functional association networks. We first examined how the parameter of the spectral clustering algorithm (i.e., the number of clusters) affects our module detection results, and demonstrated that when the number of clusters was set too small or too large the resulting module collection deteriorate in terms of gene coverage and intra-module association. We then compared our predicted modules against the randomly generated modules, and demonstrated that our modules (i) have a higher ratio of the intra-module to inter-module gene-gene functional association scores and (ii) can better capture the modularization information inherent in the experimentally verified modules. Finally we compared the module collections of seven bacterial organisms, and observed that modules related to membrane transport and cell motility are among those that are conserved among multiple organisms. Because it is desirable from both scientific and technical points of view to study functional modules at various resolution levels, we believe that the spectral clustering algorithm, with the flexibility rendered by different parameter settings, provides an appropriate solution in terms of capturing the modularization properties of networks and computational affordability.
机译:基于网络分析的模块检测在许多领域具有显着影响。在细胞/分子生物学中,基于代谢/监管网络的分析的模块检测不仅可以帮助我们更多地了解有机体的细胞机制的功能和演变,而且还将为潜在的药物目标提供易诊断的上下文信息,并促进改进药物设计。在这里,我们对基于蛋白质 - 蛋白质功能结合网络的光谱聚类来提出了对细菌的模块检测的初步研究。我们首先检查了光谱聚类算法的参数(即,集群数量)的参数如何影响我们的模块检测结果,并说明当集群的数量太小或太大时,所得模块收集在基因覆盖方面恶化和模块内联的关联。然后,我们将预测模块与随机产生的模块进行比较,并证明了我们的模块(I)与模块内模块的内部基因 - 基因功能关联分数和(ii)可以更好地捕获固有的模块化信息在实验验证的模块中。最后,我们比较了七种细菌生物的模块收集,并观察到与膜输送和细胞运动有关的模块是在多种生物中保守的模块。因为从科学和技术观点来看,我们认为在各种分辨率水平上学习功能模块,我们认为谱聚类算法具有不同参数设置的灵活性的灵活性,就捕获模块化属性提供了适当的解决方案网络和计算能力。

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