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Mining HIV protease cleavage data using genetic programming with a sum-product function

机译:使用具有和积函数的遗传程序来挖掘HIV蛋白酶切割数据

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Motivation: In order to design effective HIV inhibitors, studying and understanding the mechanism of HIV protease cleavage specification is critical. Various methods have been developed to explore the specificity of HIV protease cleavage activity. However, success in both extracting discriminant rules and maintaining high prediction accuracy is still challenging. The earlier study had employed genetic programming with a min-max scoring function to extract discriminant rules with success. However, the decision will finally be degenerated to one residue making further improvement of the prediction accuracy difficult. The challenge of revising the min-max scoring function so as to improve the prediction accuracy motivated this study. Results: This paper has designed a new scoring function called a sum-product function for extracting HIV protease cleavage discriminant rules using genetic programming methods. The experiments show that the new scoring function is superior to the min-max scoring function.
机译:动机:为了设计有效的HIV抑制剂,研究和了解HIV蛋白酶裂解规格的机制至关重要。已经开发出各种方法来探索HIV蛋白酶切割活性的特异性。然而,在提取判别规则和保持高预测精度方面的成功仍然具有挑战性。较早的研究采用具有最小-最大评分功能的遗传程序来成功提取判别规则。然而,该决定最终将退化为一个残差,使得难以进一步提高预测精度。修改最小-最大得分函数以提高预测精度的挑战激发了这项研究。结果:本文设计了一种新的计分函数,称为和积函数,用于使用遗传编程方法提取HIV蛋白酶裂解判别规则。实验表明,新的评分功能优于最小-最大评分功能。

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