双格兰杰因果关系发现的基因调控网络meta分析

G. Tam, Y. Hung, Chunqi Chang
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引用次数: 9

摘要

识别参与疾病发展的调控基因对医学进步很重要。由于存在多个实验的基因表达数据,将多个基因调控网络发现的结果结合起来,具有更高的敏感性和特异性。然而,同一问题的多个实验数据可能不具有同一组基因,因此许多现有的组合方法不适用。在本文中,我们使用一些元分析方法来解决这个问题,并比较它们的性能。仿真结果表明,Fisher卡方(FCS)族方法的计票效果优于Fisher卡方(FCS)族方法,其中FCS检验效果最好。将FCS测试应用于真实的人类HeLa细胞周期数据集,得到了组合网络的度分布,并与前人的工作进行了比较。查阅BioGRID数据库揭示了使用该方法发现的基因调控网络的生物学相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Meta-analysis on gene regulatory networks discovered by pairwise Granger causality
Identifying regulatory genes partaking in disease development is important to medical advances. Since gene expression data of multiple experiments exist, combining results from multiple gene regulatory network discoveries offers higher sensitivity and specificity. However, data for multiple experiments on the same problem may not possess the same set of genes, and hence many existing combining methods are not applicable. In this paper, we approach this problem using a number of meta-analysis methods and compare their performances. Simulation results show that vote counting is outperformed by methods belonging to the Fisher's chi-square (FCS) family, of which FCS test is the best. Applying FCS test to the real human HeLa cell-cycle dataset, degree distributions of the combined network is obtained and compared with previous works. Consulting the BioGRID database reveals the biological relevance of gene regulatory networks discovered using the proposed method.
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