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Gene-Promoter-Sequence Recognition – an Interpretable and Accurate Fuzzy-Genetic Approach

机译:基因启动子序列识别–一种可解释且准确的模糊遗传方法

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Different methods applied to gene promoter recognition share, in general, the same drawback, i.e., they are non-interpretable black-box-type techniques. The main objective of this paper is the application of our fuzzy rule-based classification approach characterized by genetically optimized accuracy-interpretability trade off (using multi-objective evolutionary optimization algorithms (M-OEOAs)) to gene promoter recognition. Two publicly accessible bacterial DNA benchmark data sets, i.e., Molecular Biology (Promoter Gene Sequences) and iPromoter-FSEn benchmark data sets are considered. For comparison purposes, two M-OEOAs are used in our experiments, i.e., the well-known Strength Pareto Evolutionary Algorithm 2 (SPEA2) and our generalization of SPEA2 (referred to as SPEA3) characterized by a higher spread and better-balanced distribution of solutions. Our results for both considered molecular biology data sets are compared with the results of 16 alternative methods (including several state-of-the-art ones) demonstrating the advantages - in terms of system's accuracy-interpretability trade-off optimization - of our approach.
机译:通常,应用于基因启动子识别的不同方法具有相同的缺点,即它们是不可解释的黑盒型技术。本文的主要目的是将我们基于模糊规则的分类方法应用于基因启动子识别,该分类方法的特点是遗传优化的准确性-可解释性折衷(使用多目标进化优化算法(M-OEOAs))。考虑了两个公众可获取的细菌DNA基准数据集,即分子生物学(启动子基因序列)和iPromoter-FSEn基准数据集。为了进行比较,我们在实验中使用了两种M-OEOA,即众所周知的强度帕累托进化算法2(SPEA2)和我们对SPEA2的推广(称为SPEA3),其特点是传播范围更大且分布更均衡解决方案。我们将两种分子生物学数据集的结果与16种替代方法(包括几种最新方法)的结果进行比较,这些方法证明了我们方法的优势-就系统的精度-可解释性折衷优化而言。

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