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Biological network inference using low order partial correlation

机译:使用低阶偏相关的生物网络推断

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Biological network inference is a major challenge in systems biology. Traditional correlation-based network analysis results in too many spurious edges since correlation cannot distinguish between direct and indirect associations. To address this issue, Gaussian graphical models (GGM) were proposed and have been widely used. Though they can significantly reduce the number of spurious edges, GGM are insufficient to uncover a network structure faithfully due to the fact that they only consider the full order partial correlation. Moreover, when the number of samples is smaller than the number of variables, further technique based on sparse regularization needs to be incorporated into GGM to solve the singular covariance inversion problem. In this paper, we propose an efficient and mathematically solid algorithm that infers biological networks by computing low order partial correlation (LOPC) up to the second order. The bias introduced by the low order constraint is minimal compared to the more reliable approximation of the network structure achieved. In addition, the algorithm is suitable for a dataset with small sample size but large number of variables. Simulation results show that LOPC yields far less spurious edges and works well under various conditions commonly seen in practice. The application to a real metabolomics dataset further validates the performance of LOPC and suggests its potential power in detecting novel biomarkers for complex disease. (C) 2014 Elsevier Inc. All rights reserved.
机译:生物网络推理是系统生物学中的主要挑战。传统的基于相关性的网络分析会导致过多的虚假边缘,因为相关性无法区分直接关联和间接关联。为了解决这个问题,提出了高斯图形模型(GGM),并已被广泛使用。尽管它们可以大大减少杂散边的数量,但是GGM不足以如实地发现网络结构,因为它们只考虑了全阶偏相关。此外,当样本数小于变量数时,需要将基于稀疏正则化的其他技术结合到GGM中,以解决奇异协方差反演问题。在本文中,我们提出了一种高效且数学上可靠的算法,该算法通过计算低阶偏相关(LOPC)直至二阶来推断生物网络。与所实现的网络结构的更可靠近似相比,由低阶约束引入的偏差最小。此外,该算法适用于样本量较小但变量众多的数据集。仿真结果表明,LOPC产生的杂散边要少得多,并且在实际中常见的各种条件下都能很好地工作。实际代谢组学数据集的应用进一步验证了LOPC的性能,并暗示了其在检测复杂疾病的新型生物标志物方面的潜在能力。 (C)2014 Elsevier Inc.保留所有权利。

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