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Normalized lmQCM: An Algorithm for Detecting Weak Quasi-Cliques in Weighted Graph with Applications in Gene Co-Expression Module Discovery in Cancers

机译:归一化的lmQCM:一种用于检测加权图中的弱拟群的算法及其在癌症基因共表达模块发现中的应用

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摘要

In this paper, we present a new approach for mining weighted networks to identify densely connected modules such as quasi-cliques. Quasi-cliques are densely connected subnetworks in a network. Detecting quasi-cliques is an important topic in data mining, with applications such as social network study and biomedicine. Our approach has two major improvements upon previous work. The first is the use of local maximum edges to initialize the search in order to avoid excessive overlaps among the modules, thereby greatly reducing the computing time. The second is the inclusion of a weight normalization procedure to enable discovery of “subtle” modules with more balanced sizes. We carried out careful tests on multiple parameters and settings using two large cancer datasets. This approach allowed us to identify a large number of gene modules enriched in both biological functions and chromosomal bands in cancer data, suggesting potential roles of copy number variations (CNVs) involved in the cancer development. We then tested the genes in selected modules with enriched chromosomal bands using The Cancer Genome Atlas data, and the results strongly support our hypothesis that the coexpression in these modules are associated with CNVs. While gene coexpression network analyses have been widely adopted in disease studies, most of them focus on the functional relationships of coexpressed genes. The relationship between coexpression gene modules and CNVs are much less investigated despite the potential advantage that we can infer from such relationship without genotyping data. Our new approach thus provides a means to carry out deep mining of the gene coexpression network to obtain both functional and genetic information from the expression data.
机译:在本文中,我们提出了一种用于挖掘加权网络以识别密集连接的模块(如准气候)的新方法。准环境是网络中密集连接的子网。在诸如社交网络研究和生物医学等应用程序中,检测准气候是数据挖掘中的重要主题。与以前的工作相比,我们的方法有两个主要改进。首先是使用局部最大边来初始化搜索,以避免模块之间的过度重叠,从而大大减少了计算时间。第二个是包含权重归一化过程,以发现具有更平衡大小的“细微”模块。我们使用两个大型癌症数据集对多个参数和设置进行了仔细的测试。这种方法使我们能够鉴定出癌症数据中生物学功能和染色体条带均丰富的大量基因模块,这表明拷贝数变异(CNV)可能参与了癌症发展。然后,我们使用The Cancer Genome Atlas数据测试了具有丰富染色体带的所选模块中的基因,结果强烈支持了我们的假设,即这些模块中的共表达与CNV相关。尽管基因共表达网络分析已在疾病研究中广泛采用,但它们大多数集中在共表达基因的功能关系上。尽管我们可以从这种关系中推断出潜在的优势而无需进行基因分型数据,但共表达基因模块与CNV之间的关系却很少研究。因此,我们的新方法提供了一种对基因共表达网络进行深度挖掘以从表达数据中获得功能和遗传信息的手段。

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