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首页> 外文期刊>Journal of Global Optimization >Analysing the scalability of multiobjective evolutionary algorithms when solving the motif discovery problem
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Analysing the scalability of multiobjective evolutionary algorithms when solving the motif discovery problem

机译:解决主题发现问题时分析多目标进化算法的可扩展性

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In this paper we analyse the scalability of seven multiobjective evolutionary algorithms when they solve large instances of a known biological problem, the motif discovery problem (MDP). The selected algorithms are a population-based and a trajectory-based algorithms (DEFT and MO-VNS, respectively), three swarm intelligence algorithms (MOABC, MO-FA, and MO-GSA), a genetic algorithm (NSGA-Ⅱ), and SPEA2. The MDP is one of the most important sequence analysis problems related to discover common patterns, motifs, in DNA sequences. A motif is a nucleic acid sequence pattern that has some biological significance as being DNA binding sites for a regulatory protein, i.e., a transcription factor (TF). A biologically relevant motif must have a certain length, be found in many sequences, and present a high similarity among the subsequences which compose it. These three goals are in conflict with each other, therefore a multiobjective approach is a good way of facing the MDP. In addition, in recent years, scientists are decoding genomes of many organisms, increasing the computational workload of the algorithms. Therefore, we need algorithms that are able to deal with these new large DNA instances. The obtained experimental results suggest that MOABC and MO-FA are the algorithms with the best scalability behaviours.
机译:在本文中,我们分析了七种多目标进化算法在解决已知生物学问题(模体发现问题(MDP))的大型实例时的可扩展性。选择的算法是基于种群和基于轨迹的算法(分别为DEFT和MO-VNS),三种群智能算法(MOABC,MO-FA和MO-GSA),遗传算法(NSGA-Ⅱ),和SPEA2。 MDP是与发现DNA序列中的常见模式,基序有关的最重要的序列分析问题之一。基序是具有一定生物学意义的核酸序列模式,它是调节蛋白即转录因子(TF)的DNA结合位点。与生物学相关的基序必须具有一定的长度,可以在许多序列中找到,并且在组成该基序的子序列之间具有高度相似性。这三个目标相互冲突,因此多目标方法是面对MDP的好方法。另外,近年来,科学家正在解码许多生物的基因组,从而增加了算法的计算量。因此,我们需要能够处理这些新的大型DNA实例的算法。实验结果表明,MOABC和MO-FA是具有最佳可扩展性的算法。

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