机构地区: 广东工业大学计算机学院
出 处: 《计算机应用》 2007年第1期80-83,共4页
摘 要: 在综述了T细胞表位预测的定义,意义和研究现状的基础上,分析了当前流行的基于误差反向传播前馈神经网络(BPNN)的T细胞表位预测模型的不足,即网络结构较难确定、训练速度慢和难以增量学习等,提出了利用排序学习前向掩蔽(SLAM)模型及其增量学习算法作为T细胞表位预测方法,并给出了构建T细胞表位预测模型的基本步骤。基因HLA-DR4(B1*0401)编码的MHC II类分子结合肽的应用实例表明,与基于BPNN的T细胞表位预测模型相比,基于SLAM的T细胞表位预测模型不但能在极短时间内完成样本的学习,而且能有效地实现增量学习。 The definition, the meaning and the state-of-art of T cell epitope prediction were firstly summarized. And then, the disadvantages of the prevailing T cell epitope prediction model based on the Back-Propagation Neural Networks (BPNN), including difficulties in presetting networks structure, converging and incremental learning, were investigated. In terms of the above-mentioned drawbacks, Sequential Learning Ahead Masking model (SLAM) and its fast incremental learning algorithm were deliberately chosen to predict T cell epitope. Meanwhile, the basic steps of constructing T cell epitope prediction model based on SLAM were advocated. Finally, a case study of predicting the binding capacities to MHC class II molecule encoded by gene HLA-DR4 ( B1 * 0401.) was given in detail. The application results show that T cell epitope prediction model based on SLAM has better learning performance and stronger incremental learning capabilities than that based on conventional BPNN.