基于微阵列数据的多目标混合SPEA2+遗传网络推断

Dilruba Showkat, M. Kabir
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引用次数: 5

摘要

多目标优化在优化许多现实生活问题中起着重要作用,我们希望优化多个目标。研究中存在许多多目标优化算法。NSGA-II和SPEA2是应用广泛的多目标优化算法。SPEA2+算法在搜索和保持最优解的多样性方面优于其他多目标优化算法。在本研究中,我们提出了一种新的基于Hybrid SPEA2+算法的推理方法来重构基因调控网络。为了更精确地获得稀疏基因网络结构,我们提出了一个新的目标函数。为了对基因调控网络进行逆向工程,我们使用了线性时变模型。该方法首先针对合成无噪声时间序列数据集进行了测试。它成功地从无噪声时间序列数据集中推断出所有正确的规律。然后将其应用于合成噪声时间序列数据集。即使存在噪声,所提出的方法也能正确捕获所有正确的基因调控。通过分析大肠杆菌SOS DNA修复系统的真实基因表达数据集,进一步验证了所提出的重建方法。我们提出的方法在寻找更正确的调控方面显示出其潜力,并通过与其他现有研究结果的比较证实了这一点。
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Inference of genetic networks using multi-objective hybrid SPEA2+ from Microarray data
Multi-objective optimization plays a significant role in optimizing many real life problems, where we desire to optimize more than one objective. Numerous multi-objective optimization algorithm exists in research. NSGA-II and SPEA2 are widely used multi-objective optimization algorithms. SPEA2+ algorithm performs better than the other multi-objective optimization algorithms in terms of searching and maintaining diversity in the optimal solution. In this research, to reconstruct the gene regulatory network we have proposed a new Hybrid SPEA2+ algorithm based inference method. We have proposed a new objective function to obtain sparse gene network structure more precisely. To reverse engineer the gene regulatory network we have used linear time variant model. The proposed approach is at first tested against synthetic noise free time series datasets. It has successfully inferred all the correct regulations from noise free time series datasets. Then it was applied on synthetic noisy time series datasets. Even with the presence of noise, the proposed method have correctly captured all the correct gene regulations successfully. The proposed reconstruction method has been further validated by analyzing the real gene expression datasets of SOS DNA repair system in Escherichia coli. Our proposed method have shown its potency in finding more correct regulations and this has been confirmed by comparing the obtained gene regulations with the results of other existing researches.
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