利用多种群辅助量子遗传算法预测RNA二级结构

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY
Human Heredity Pub Date : 2019-08-28 DOI:10.1159/000501480
Sha Shi, Xin-Li Zhang, Xian-Li Zhao, Le Yang, Wei Du, Yun-Jiang Wang
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引用次数: 10

摘要

量子启发遗传算法(QGAs)最近被引入到RNA二级结构的预测中,并且它们比现有的流行策略显示出一些优势。本文针对RNA二级结构预测,提出了一种新的量子遗传算法——多群体辅助量子遗传算法(MAQGA)。与现有的QGA相比,我们的策略涉及多个种群,这些种群在每次迭代中以合作的方式一起进化,并且不同种群之间的遗传交换通过算子转移操作来执行。数值结果表明,使用我们的方法可以显著提高现有遗传算法(进化算法[EAs])的性能,包括传统的进化算法和QGA。此外,对于中短长度的RNA序列,MAQGA甚至在预测准确性和灵敏度方面改进了这种最先进的软件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prediction of the RNA Secondary Structure Using a Multi-Population Assisted Quantum Genetic Algorithm
Quantum-inspired genetic algorithms (QGAs) were recently introduced for the prediction of RNA secondary structures, and they showed some superiority over the existing popular strategies. In this paper, for RNA secondary structure prediction, we introduce a new QGA named multi-population assisted quantum genetic algorithm (MAQGA). In contrast to the existing QGAs, our strategy involves multi-populations which evolve together in a cooperative way in each iteration, and the genetic exchange between various populations is performed by an operator transfer operation. The numerical results show that the performances of existing genetic algorithms (evolutionary algorithms [EAs]), including traditional EAs and QGAs, can be significantly improved by using our approach. Moreover, for RNA sequences with middle-short length, the MAQGA improves even this state-of-the-art software in terms of both prediction accuracy and sensitivity.
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来源期刊
Human Heredity
Human Heredity 生物-遗传学
CiteScore
2.50
自引率
0.00%
发文量
12
审稿时长
>12 weeks
期刊介绍: Gathering original research reports and short communications from all over the world, ''Human Heredity'' is devoted to methodological and applied research on the genetics of human populations, association and linkage analysis, genetic mechanisms of disease, and new methods for statistical genetics, for example, analysis of rare variants and results from next generation sequencing. The value of this information to many branches of medicine is shown by the number of citations the journal receives in fields ranging from immunology and hematology to epidemiology and public health planning, and the fact that at least 50% of all ''Human Heredity'' papers are still cited more than 8 years after publication (according to ISI Journal Citation Reports). Special issues on methodological topics (such as ‘Consanguinity and Genomics’ in 2014; ‘Analyzing Rare Variants in Complex Diseases’ in 2012) or reviews of advances in particular fields (‘Genetic Diversity in European Populations: Evolutionary Evidence and Medical Implications’ in 2014; ‘Genes and the Environment in Obesity’ in 2013) are published every year. Renowned experts in the field are invited to contribute to these special issues.
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