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Protein complex detection algorithm based on multiple topological characteristics in PPI networks

机译:基于PPI网络多拓扑特性的蛋白质复杂检测算法

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Detecting protein complexes from available protein-protein interaction (PPI) networks is an important task, and several related algorithms have been proposed. These algorithms usually consider a single topological metric and ignore the rich topological characteristics and inherent organization information of protein complexes. However, the effective use of such information is crucial to protein complex detection. To overcome this deficiency, this study presents a heuristic clustering algorithm to identify protein complexes by fully exploiting the topological information of PPI networks. By considering the clustering coefficient and the node degree, a new nodal metric is proposed to quantify the importance of each node within a local subgraph. An iterative paradigm is used to incrementally identify seed proteins and expand each seed to a cluster. First, among the unclustered nodes, the node with the highest nodal metric is selected as a new seed. Then, the seed is expanded to a cluster by adding candidate nodes recursively from its neighbors according to both the density of the cluster and the connection between a candidate node and the cluster. The experimental results demonstrate that the proposed algorithm outperforms other competing algorithms in terms of F-measure and accuracy. (C) 2019 Elsevier Inc. All rights reserved.
机译:检测可用蛋白质 - 蛋白质相互作用(PPI)网络的蛋白质复合物是一个重要的任务,并且已经提出了几种相关算法。这些算法通常考虑单个拓扑度量,忽略丰富的拓扑特征和蛋白质复合物的固有组织信息。然而,这些信息的有效使用对于蛋白质复杂检测至关重要。为了克服这种缺陷,本研究提出了一种通过充分利用PPI网络的拓扑信息来识别蛋白质复合物的启发式聚类算法。通过考虑聚类系数和节点度,提出了一种新的节点度量来量化本地子图中每个节点的重要性。迭代范式用于逐渐识别种子蛋白并将每种种子扩展到簇。首先,在未刻板的节点中,选择具有最高节点度量的节点作为新种子。然后,通过根据簇的密度和候选节点和群集之间的连接,通过从其邻居从其邻居添加候选节点并在候选节点和群集之间的连接来递归地扩展到群集。实验结果表明,所提出的算法在F测量和准确性方面优于其他竞争算法。 (c)2019 Elsevier Inc.保留所有权利。

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