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An iterative network partition algorithm for accurate identification of dense network modules

机译:精确识别密集网络模块的迭代网络分区算法

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摘要

A key step in network analysis is to partition a complex network into dense modules. Currently, modularity is one of the most popular benefit functions used to partition network modules. However, recent studies suggested that it has an inherent limitation in detecting dense network modules. In this study, we observed that despite the limitation, modularity has the advantage of preserving the primary network structure of the undetected modules. Thus, we have developed a simple iterative Network Partition (iNP) algorithm to partition a network. The iNP algorithm provides a general framework in which any modularity-based algorithm can be implemented in the network partition step. Here, we tested iNP with three modularity-based algorithms: multi-step greedy (MSG), spectral clustering and Qcut. Compared with the original three methods, iNP achieved a significant improvement in the quality of network partition in a benchmark study with simulated networks, identified more modules with significantly better enrichment of functionally related genes in both yeast protein complex network and breast cancer gene co-expression network, and discovered more cancer-specific modules in the cancer gene co-expression network. As such, iNP should have a broad application as a general method to assist in the analysis of biological networks.
机译:网络分析的关键步骤是将复杂的网络划分为密集的模块。当前,模块化是用于划分网络模块的最流行的好处功能之一。但是,最近的研究表明,它在检测密集网络模块方面具有固有的局限性。在这项研究中,我们观察到,尽管有局限性,模块化仍具有保留未检测模块的主要网络结构的优势。因此,我们开发了一种简单的迭代网络分区(iNP)算法来对网络进行分区。 iNP算法提供了一个通用框架,其中可以在网络分区步骤中实现任何基于模块化的算法。在这里,我们使用三种基于模块化的算法测试了iNP:多步贪婪(MSG),频谱聚类和Qcut。与原始的三种方法相比,iNP在模拟网络的基准研究中网络划分的质量有了显着提高,在酵母蛋白复合物网络和乳腺癌基因共表达中,发现了更多的模块,这些模块具有功能相关基因的明显更好的富集网络,并在癌症基因共表达网络中发现了更多的癌症特定模块。因此,iNP应该作为协助分析生物网络的通用方法而具有广泛的应用。

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