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Multiobjective optimization to reconstruct biological networks

机译:重构生物网络的多目标优化

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摘要

Automated methods for reconstructing biological networks are becoming increasingly important in computational systems biology. Public databases containing information on biological processes for hundreds of organisms are assisting in the inference of such networks. This paper proposes a multiobjective genetic algorithm method to reconstruct networks related to metabolism and protein interaction. Such a method utilizes structural properties of scale-free networks and known biological information about individual genes and proteins to reconstruct metabolic networks represented as enzyme graph and protein interaction networks. We test our method on four commonly-used protein networks in yeast. Two are networks related to the metabolism of the yeast: KEGG and BioCyc. The other two datasets are networks from protein-protein interaction: Krogan and BioGrid. Experimental results show that the proposed method is capable of reconstructing biological networks by combining different omics data and structural characteristics of scale-free networks. However, the proposed method to reconstruct the network is time-consuming because several evaluations must be performed. We parallelized this method on GPU to overcome this limitation by parallelizing the objective functions of the presented method. The parallel method shows a significant reduction in the execution time over the GPU card which yields a 492-fold speedup.
机译:用于重建生物网络的自动化方法在计算系统生物学中变得越来越重要。包含有关数百个生物的生物过程信息的公共数据库正在协助这些网络的推动。本文提出了一种重建与新陈代谢和蛋白质相互作用相关网络的多目标遗传算法方法。这种方法利用无规模网络和有关个体基因和蛋白质的已知生物信息的结构特性,以重建代谢网络表示为酶图和蛋白质相互作用网络。我们在酵母中的四种常用蛋白质网络上测试我们的方法。两个是与酵母新陈代谢相关的网络:Kegg和Biocyc。另外两个数据集是来自蛋白质 - 蛋白质相互作用的网络:Krogan和BioGrid。实验结果表明,该方法能够通过组合不同的OMICS数据和无规模网络的结构特征来重建生物网络。但是,建议的重建方法是耗时,因为必须执行几个评估。我们并将这种方法并联在GPU上通过并行并行化所提出的方法的目标函数来克服这种限制。并行方法显示在GPU卡上的执行时间显着降低,其产生492倍的加速。

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