摘要
剪接位点识别是基因识别中的关键环节。本文对待测样本采用0/1编码,以表征各位置上的碱基,并结合碱基二联体出现的频次,最后采用支持向量机(SVM)进行分类决策。HS3D数据集上的仿真结果显示,本方法获得的预测精度为92.84%。
splicing site recognition is the key link in gene recognition. In this paper, the test samples are encoded with 0 / 1 encoding to represent the bases at each position, and the occurrence frequency of the base dimer is combined. Finally, support vector machine ( SVM) is adopted to make classification decisions. The simulation results on HS3D data set show that the prediction accuracy obtained by this method is 92. 84%.
出处
《数码设计》
2018年第12期82-82,共1页
Peak Data Science
基金
湖南农业大学东方科技学院2016年青年科学基金项目(16QNZ01):基于机器学习的分子序列信号位点识别研究.
关键词
剪接位点
基因识别
支持向量机(SVM)
0/1编码
splicing site
splicing site Gene identification
Support vector machines ( SVM)
0 / 1 coding