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Gene Regulation Network Inference With Joint Sparse Gaussian Graphical Models

机译:联合稀疏高斯图形模型的基因调控网络推论

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摘要

Revealing biological networks is one key objective in systems biology. With microarrays, researchers now routinely measure expression profiles at the genome level under various conditions, and such data may be used to statistically infer gene regulation networks. Gaussian graphical models (GGMs) have proven useful for this purpose by modeling the Markovian dependence among genes. However, a single GGM may not be adequate to describe the potentially differing networks across various conditions, and hence it is more natural to infer multiple GGMs from such data. In this article we propose a class of nonconvex penalty functions aiming at the estimation of multiple GGMs with a flexible joint sparsity constraint. We illustrate the property of our proposed nonconvex penalty functions by simulation study. We then apply the method to a gene expression dataset from the GenCord Project, and show that our method can identify prominent pathways across different conditions. Supplementary materials for this article are available online.
机译:揭示生物网络是系统生物学的主要目标之一。利用微阵列,研究人员现在可以在各种条件下常规地在基因组水平上测量表达谱,这些数据可用于统计推断基因调控网络。高斯图形模型(GGM)已证明可以通过对基因之间的马尔可夫依赖性进行建模来实现此目的。但是,单个GGM可能不足以描述跨各种条件的潜在不同网络,因此从此类数据推断多个GGM更为自然。在本文中,我们提出了一类非凸罚函数,旨在估计具有灵活联合稀疏约束的多个GGM。我们通过仿真研究说明了我们提出的非凸罚函数的性质。然后,我们将该方法应用于GenCord项目的基因表达数据集,并表明我们的方法可以识别出跨越不同条件的重要途径。可在线获得本文的补充材料。

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