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Conditional mutual inclusive information enables accurate quantification of associations in gene regulatory networks

机译:有条件的相互包容性信息可以准确定量基因调控网络中的关联

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Mutual information (MI), a quantity describing the nonlinear dependence between two random variables, has been widely used to construct gene regulatory networks (GRNs). Despite its good performance, MI cannot separate the direct regulations from indirect ones among genes. Although the conditional mutual information (CMI) is able to identify the direct regulations, it generally underestimates the regulation strength, i.e. it may result in false negatives when inferring gene regulations. In this work, to overcome the problems, we propose a novel concept, namely conditional mutual inclusive information (CMI2), to describe the regulations between genes. Furthermore, with CMI2, we develop a new approach, namely CMI2NI (CMI2-based network inference), for reverse-engineering GRNs. In CMI2NI, CMI2 is used to quantify the mutual information between two genes given a third one through calculating the Kullback-Leibler divergence between the postulated distributions of including and excluding the edge between the two genes. The benchmark results on the GRNs from DREAM challenge as well as the SOS DNA repair network in Escherichia coli demonstrate the superior performance of CMI2NI. Specifically, even for gene expression data with small sample size, CMI2NI can not only infer the correct topology of the regulation networks but also accurately quantify the regulation strength between genes. As a case study, CMI2NI was also used to reconstruct cancer-specific GRNs using gene expression data from The Cancer Genome Atlas (TCGA).
机译:互信息(MI)是描述两个随机变量之间的非线性依赖性的量,已被广泛用于构建基因调控网络(GRN)。尽管MI具有良好的性能,但它不能将直接调控与基因间的间接调控区分开。尽管条件共有信息(CMI)能够识别直接的法规,但它通常会低估法规强度,即在推断基因法规时可能会导致假阴性。在这项工作中,为了克服这些问题,我们提出了一个新颖的概念,即条件互斥信息(CMI2),来描述基因之间的调控。此外,借助CMI2,我们为逆向工程GRN开发了一种新方法,即CMI2NI(基于CMI2的网络推论)。在CMI2NI中,CMI2用于通过计算假定的包括和排除两个基因之间的边缘之间的分布之间的Kullback-Leibler散度,对给定第三个基因的两个基因之间的相互信息进行量化。来自DREAM挑战的GRN以及大肠杆菌中SOS DNA修复网络的基准测试结果证明了CMI2NI的卓越性能。具体而言,即使对于样本量小的基因表达数据,CMI2NI不仅可以推断出调控网络的正确拓扑结构,而且可以准确地定量基因之间的调控强度。作为一个案例研究,CMI2NI还被用于利用癌症基因组图谱(TCGA)的基因表达数据重建癌症特异性GRN。

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