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Comparison of module detection algorithms in protein networks and investigation of the biological meaning of predicted modules

机译:蛋白质网络中模块检测算法的比较和预测模块的生物学意义研究

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摘要

BackgroundIt is generally acknowledged that a functional understanding of a biological system can only be obtained by an understanding of the collective of molecular interactions in form of biological networks. Protein networks are one particular network type of special importance, because proteins form the functional base units of every biological cell. On a mesoscopic level of protein networks, modules are of significant importance because these building blocks may be the next elementary functional level above individual proteins allowing to gain insight into fundamental organizational principles of biological cells.ResultsIn this paper, we provide a comparative analysis of five popular and four novel module detection algorithms. We study these module prediction methods for simulated benchmark networks as well as 10 biological protein interaction networks (PINs). A particular focus of our analysis is placed on the biological meaning of the predicted modules by utilizing the Gene Ontology (GO) database as gold standard for the definition of biological processes. Furthermore, we investigate the robustness of the results by perturbing the PINs simulating in this way our incomplete knowledge of protein networks.ConclusionsOverall, our study reveals that there is a large heterogeneity among the different module prediction algorithms if one zooms-in the biological level of biological processes in the form of GO terms and all methods are severely affected by a slight perturbation of the networks. However, we also find pathways that are enriched in multiple modules, which could provide important information about the hierarchical organization of the system.
机译:背景技术人们普遍认为,只有通过了解生物网络形式的分子相互作用的集合,才能获得对生物系统的功能性理解。蛋白质网络是一种特别重要的网络类型,因为蛋白质形成了每个生物细胞的功能性基本单位。在蛋白质网络的介观水平上,模块非常重要,因为这些构建模块可能是单个蛋白质之上的下一个基本功能水平,从而使您能够洞悉生物细胞的基本组织原理。结果在本文中,我们对五个方面进行了比较分析。流行的四种新颖的模块检测算法。我们研究了用于模拟基准网络以及10种生物蛋白质相互作用网络(PIN)的这些模块预测方法。我们的分析重点是通过利用基因本体论(GO)数据库作为生物过程定义的黄金标准,来预测模块的生物学意义。此外,我们通过扰动以这种方式模拟我们不完整的蛋白质网络知识的PIN来研究结果的鲁棒性。结论总体而言,我们的研究表明,如果一个模块放大生物学水平,则模块预测算法之间存在很大的异质性。 GO术语形式的生物过程和所有方法都会受到网络的轻微干扰而受到严重影响。但是,我们还发现了包含多个模块的途径,这些途径可以提供有关系统层次结构的重要信息。

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