基于核相关度量的基因互作网络。

Q4 Pharmacology, Toxicology and Pharmaceutics International Journal of Computational Biology and Drug Design Pub Date : 2013-01-01 Epub Date: 2013-02-21 DOI:10.1504/IJCBDD.2013.052203
Lijun Cheng, K Khorasani, Yongsheng Ding, Xihong Guo
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引用次数: 1

摘要

本文提出一种核相关系数(KCC)方法来作为距离度量来阐明基因的非线性关系。为了评估这种非线性距离度量的性能,利用图论构造了酵母基因公共数据集上的高斯核生物网络。具体地,分析了该方法的分布和性质,并与经典的Pearson相关方法进行了比较。我们提出的核相关度量的可靠性和优势在DREAM(逆向工程评估和方法对话)项目的十个演示中得到验证和正式展示。测试实验结果表明,所提出的核相关系数测度具有较强的相互作用基因识别能力,与常用的Pearson相关测度和互信息测度相比,所提出的方法能够准确地检测出关键基因和功能相互作用(也称为派系)。
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Gene interaction networks based on kernel correlation metrics.

In this paper, a Kernel correlation coefficient (KCC) method is proposed to elucidate the gene nonlinear relationships as a distance metric. To evaluate the performance of this nonlinear distance measure, a biological network of the Gaussian Kernel on a public dataset of yeast genes is constructed by using a graph theory. Specifically, the distribution and properties of this new measure are analysed and compared with the classical Pearson correlation method. The reliability and advantages of our proposed Kernel correlation metric is verified and shown formally on ten showcases of the DREAM (Dialogue for Reverse Engineering Assessments and Methods) project. Test experiment results demonstrate that the proposed Kernel correlation coefficient measure has a strong capability in identifying interaction genes, and that the proposed method can detect accurately the key genes and functional interactions (also known as the cliques) as compared to the commonly used Pearson correlation and Mutual Information measures.

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来源期刊
International Journal of Computational Biology and Drug Design
International Journal of Computational Biology and Drug Design Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
1.00
自引率
0.00%
发文量
8
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