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Learning causal networks from systems biology time course data: an effective model selection procedure for the vector autoregressive process

机译:从系统生物学时间过程数据中学习因果网络:矢量自回归过程的有效模型选择过程

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Background Causal networks based on the vector autoregressive (VAR) process are a promising statistical tool for modeling regulatory interactions in a cell. However, learning these networks is challenging due to the low sample size and high dimensionality of genomic data. Results We present a novel and highly efficient approach to estimate a VAR network. This proceeds in two steps: (i) improved estimation of VAR regression coefficients using an analytic shrinkage approach, and (ii) subsequent model selection by testing the associated partial correlations. In simulations this approach outperformed for small sample size all other considered approaches in terms of true discovery rate (number of correctly identified edges relative to the significant edges). Moreover, the analysis of expression time series data from Arabidopsis thaliana resulted in a biologically sensible network. Conclusion Statistical learning of large-scale VAR causal models can be done efficiently by the proposed procedure, even in the difficult data situations prevalent in genomics and proteomics. Availability The method is implemented in R code that is available from the authors on request.
机译:基于向量自回归(VAR)过程的背景因果网络是一种有前途的统计工具,可用于建模细胞中的调控相互作用。但是,由于基因组数据的样本量少且维数高,因此学习这些网络具有挑战性。结果我们提出了一种新颖且高效的方法来估算VAR网络。这分两个步骤进行:(i)使用分析收缩方法改进VAR回归系数的估计,以及(ii)通过测试相关的局部相关性进行后续模型选择。在模拟中,就小样本量而言,该方法的表现优于其他所有考虑的方法(在真实发现率(相对于有效边缘而言正确识别的边缘数)方面)。此外,来自拟南芥的表达时间序列数据的分析产生了生物学上敏感的网络。结论即使在基因组学和蛋白质组学中普遍存在的困难数据情况下,通过提出的程序也可以有效地完成大规模VAR因果模型的统计学习。可用性该方法以R代码实现,可应要求提供给作者。

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