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Grouped graphical Granger modeling for gene expression regulatory networks discovery

机译:用于基因表达调控网络发现的分组图形化格兰杰建模

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We consider the problem of discovering gene regulatory networks from time-series microarray data. Recently, graphical Granger modeling has gained considerable attention as a promising direction for addressing this problem. These methods apply graphical modeling methods on time-series data and invoke the notion of 'Granger causality' to make assertions on causality through inference on time-lagged effects. Existing algorithms, however, have neglected an important aspect of the problem-the group structure among the lagged temporal variables naturally imposed by the time series they belong to. Specifically, existing methods in computational biology share this shortcoming, as well as additional computational limitations, prohibiting their effective applications to the large datasets including a large number of genes and many data points. In the present article, we propose a novel methodology which we term 'grouped graphical Granger modeling method', which overcomes the limitations mentioned above by applying a regression method suited for high-dimensional and large data, and by leveraging the group structure among the lagged temporal variables according to the time series they belong to. We demonstrate the effectiveness of the proposed methodology on both simulated and actual gene expression data, specifically the human cancer cell (HeLa S3) cycle data. The simulation results show that the proposed methodology generally exhibits higher accuracy in recovering the underlying causal structure. Those on the gene expression data demonstrate that it leads to improved accuracy with respect to prediction of known links, and also uncovers additional causal relationships uncaptured by earlier works.
机译:我们考虑从时序微阵列数据中发现基因调控网络的问题。最近,图形化的格兰杰建模已经得到了相当大的关注,作为解决该问题的有希望的方向。这些方法将图形建模方法应用于时间序列数据,并调用“格兰杰因果关系”概念以通过推断时间滞后效应来对因果关系进行断言。但是,现有算法已忽略了该问题的一个重要方面-由它们所属的时间序列自然产生的滞后时间变量之间的组结构。具体而言,计算生物学中的现有方法共有此缺点以及其他计算限制,从而禁止将其有效地应用于包括大量基因和许多数据点的大型数据集。在本文中,我们提出了一种新的方法,称为“分组图形Granger建模方法”,它通过应用适用于高维和大数据的回归方法并利用滞后的群体结构来克服了上述限制。根据它们所属的时间序列的时间变量。我们在模拟和实际基因表达数据,特别是人类癌细胞(HeLa S3)周期数据上证明了所提出方法的有效性。仿真结果表明,所提出的方法通常在恢复潜在因果结构方面表现出更高的准确性。基因表达数据上的那些证明,它导致已知链接预测的准确性提高,并且还发现了早期工作未捕获的其他因果关系。

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