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Estimating equation–based causality analysis with application to microarray time series data

机译:估计基于方程的因果关系分析并应用于微阵列时间序列数据

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摘要

Microarray time-course data can be used to explore interactions among genes and infer gene network. The crucial step in constructing gene network is to develop an appropriate causality test. In this regard, the expression profile of each gene can be treated as a time series. A typical existing method establishes the Granger causality based on Wald type of test, which relies on the homoscedastic normality assumption of the data distribution. However, this assumption can be seriously violated in real microarray experiments and thus may lead to inconsistent test results and false scientific conclusions. To overcome the drawback, we propose an estimating equation–based method which is robust to both heteroscedasticity and nonnormality of the gene expression data. In fact, it only requires the residuals to be uncorrelated. We will use simulation studies and a real-data example to demonstrate the applicability of the proposed method.
机译:微阵列时程数据可用于探索基因之间的相互作用和推断基因网络。构建基因网络的关键步骤是开发适当的因果关系检验。在这方面,每个基因的表达谱可被视为时间序列。现有的一种典型方法是基于Wald型检验建立Granger因果关系,该检验依赖于数据分布的同方正态性假设。但是,这种假设可能在实际的微阵列实验中被严重违反,因此可能导致不一致的测试结果和错误的科学结论。为了克服这一缺点,我们提出了一种基于估计方程的方法,该方法对基因表达数据的异方差性和非正态性均具有鲁棒性。实际上,它仅要求残差不相关。我们将使用仿真研究和一个实际数据示例来证明该方法的适用性。

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