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Modules identification in gene positive networks of hepatocellular carcinoma using pearson agglomerative method and Pearson cohesion coupling modularity

机译:利用Pearson凝聚法和Pearson内聚耦合模块对肝癌基因阳性网络中的模块进行识别

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摘要

In this study, a gene positive network is proposed based on a weighted undirected graph, where the weight represents the positive correlation of the genes. A Pearson agglomerative clustering algorithm is employed to build a clustering tree, where dotted lines cut the tree from bottom to top leading to a number of subsets of the modules. In order to achieve better module partitions, the Pearson correlation coefficient modularity is addressed to seek optimal module decomposition by selecting an optimal threshold value. For the liver cancer gene network under study, we obtain a strong threshold value at 0.67302, and a very strong correlation threshold at 0.80086. On the basis of these threshold values, fourteen strong modules and thirteen very strong modules are obtained respectively. A certain degree of correspondence between the two types of modules is addressed as well. Finally, the biological significance of the two types of modules is analyzed and explained, which shows that these modules are closely related to the proliferation and metastasis of liver cancer. This discovery of the new modules may provide new clues and ideas for liver cancer treatment.
机译:在这项研究中,基于加权无向图提出了基因阳性网络,其中权重代表基因的正相关性。使用Pearson聚集聚类算法构建聚类树,其中虚线从下到上将树切开,从而导致模块的多个子集。为了实现更好的模块划分,解决了Pearson相关系数模块化问题,以通过选择最佳阈值来寻求最佳模块分解。对于正在研究的肝癌基因网络,我们获得了很强的阈值0.67302和非常强的相关阈值0.80086。基于这些阈值,分别获得了十四个强模块和十三个非常强模块。还解决了两种类型的模块之间的某种程度的对应关系。最后,对这两种模块的生物学意义进行了分析和解释,表明这些模块与肝癌的增殖和转移密切相关。新模块的发现可能为肝癌治疗提供新的线索和思路。

著录项

  • 作者

    Hu, Jinyu; Gao, Zhiwei;

  • 作者单位
  • 年度 2012
  • 总页数
  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
  • 中图分类

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