Inference of genetic regulatory networks with unknown covariance structure

Belhassen Bayar, N. Bouaynaya, R. Shterenberg
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引用次数: 1

Abstract

The major challenge in reverse-engineering genetic regulatory networks is the small number of (time) measurements or experiments compared to the number of genes, which makes the system under-determined and hence unidentifiable. The only way to overcome the identifiability problem is to incorporate prior knowledge about the system. It is often assumed that genetic networks are sparse. In addition, if the measurements, in each experiment, present an unknown correlation structure, then the estimation problem becomes even more challenging. Estimating the covariance structure will improve the estimation of the network connectivity but will also make the estimation of the already under-determined problem even more challenging. In this paper, we formulate reverse-engineering genetic networks as a multiple linear regression problem. We show that, if the number of experiments is smaller than the number of genes and if the measurements present an unknown covariance structure, then the likelihood function diverges, making the maximum likelihood estimator senseless. We subsequently propose a normalized likelihood function that guarantees convergence while keeping the form of the Gaussian distribution. The optimal connectivity matrix is approximated as the solution of a convex optimization problem. Our simulation results show that the proposed maximum normalized-likelihood estimator outperforms the classical regularized maximum likelihood estimator, which assumes a known covariance structure.
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未知协方差结构的遗传调控网络推断
逆向工程基因调控网络的主要挑战是与基因数量相比,测量或实验的数量(时间)较少,这使得系统不确定,因此无法识别。克服可识别性问题的唯一方法是结合关于系统的先验知识。人们通常认为遗传网络是稀疏的。此外,如果每次实验中的测量都呈现未知的相关结构,那么估计问题就变得更具挑战性。协方差结构的估计将改善网络连通性的估计,但也将使已经不确定的问题的估计更具挑战性。在本文中,我们将逆向工程遗传网络表述为一个多元线性回归问题。我们表明,如果实验的数量小于基因的数量,并且如果测量结果呈现未知的协方差结构,那么似然函数就会发散,使最大似然估计器失去意义。我们随后提出了一个标准化的似然函数,保证收敛,同时保持高斯分布的形式。将最优连通性矩阵近似为一个凸优化问题的解。仿真结果表明,所提出的最大归一化似然估计量优于假设已知协方差结构的经典正则化最大似然估计量。
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