首页> 外文会议>2012 IEEE International Conference on Bioinformatics and Biomedicine. >Rotation crossover and K-site move mutation for evolutionary protein folding in 3D FCC HP model (preliminary version)
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Rotation crossover and K-site move mutation for evolutionary protein folding in 3D FCC HP model (preliminary version)

机译:旋转交叉和K位点移动突变,用于3D FCC HP模型中的进化蛋白折叠(初步版本)

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In this paper we present a new evolutionary algorithm for the protein folding problem. We study the problem in the 3D FCC HP model which has been widely used in previous research. Our focus is to develop evolutionary algorithms (EA) which are robust, easy to operate and can handle various energy functions. We propose lattice rotation for crossover and K-site move for mutation, which form the key components of our evolutionary algorithms. Experiment shows that our algorithms are able to find minimum-energy conformations for many sequences whose optimal conformations are not found in previous EA-based algorithms. Furthermore, our idea can be easily integrated into Monte Carlo and Tabu searches as approaches for local searches.
机译:在本文中,我们提出了一种针对蛋白质折叠问题的新进化算法。我们在3D FCC HP模型中研究了该问题,该模型已在先前的研究中广泛使用。我们的重点是开发功能强大,易于操作且可以处理各种能源功能的进化算法(EA)。我们提出用于交叉的晶格旋转和用于突变的K位点移动,这些构成了我们进化算法的关键组成部分。实验表明,我们的算法能够找到许多序列的最小能量构象,而这些序列的最佳构象在以前基于EA的算法中找不到。此外,我们的想法可以轻松地集成到Monte Carlo和Tabu搜索中,作为本地搜索的方法。

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