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Frequency domain discovery of gene regulatory networks

机译:基因调控网络的频域发现

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Discovery of gene regulatory network (GRN) from gene expression data gives an insight into tumor developments and underlying structures. Granger causality (GC) is considered as a powerful tool to detect the interactions between elements of a network. Among the various methods suggested for GC, we use Pairwise GC (PGC), Kernel GC (KGC) and Correntropy method. Also GC is defined in two domains. In time domain, GC cannot correctly determine how strongly one time series influences the other when there is directional causality between them, this limitation necessitates an alternative method. In this regard, GC in frequency domain is being applied as a solution. In this paper, first, we conduct a frequency domain analysis on these methods theoretically. We then evaluate the performance of PGC in both domains by applying real HeLa dataset with three experiments and compare it with previous work. Finally, we apply all methods to both synthetic data and a 94-gene HeLa data to illustrate the discovered networks. We show that frequency domain has better performance in discovery of relations at all experiments.
机译:从基因表达数据发现基因调节网络(GRN)介绍肿瘤发育和潜在的结构。格兰杰因果关系(GC)被认为是检测网络元素之间的交互的强大工具。在针对GC的各种方法中,我们使用成对GC(PGC),内核GC(KGC)和控制方法。此外,GC也定义在两个域中。在时域中,GC无法正确地确定当存在方向性因果关系时,在它们之间有一个时间序列的强烈影响,这种限制需要一种替代方法。在这方面,频域中的GC被应用为解决方案。在本文中,首先,我们理论上对这些方法进行频域分析。然后,我们通过使用三个实验应用真正的Hela数据集来评估PGC在两个域中的性能,并将其与以前的工作进行比较。最后,我们将所有方法应用于合成数据和94-Gene Hela数据,以说明被发现的网络。我们表明频域在发现所有实验中的关系方面具有更好的性能。

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