一种结合支持向量机和马尔可夫模型的剪接位置识别方法

Elham Pashaei, Alper Yilmaz, N. Aydin
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引用次数: 10

摘要

由于生物序列数据呈指数级增长,基因检测已成为计算生物学中具有挑战性的任务之一。剪接位点预测是基因检测的重要组成部分。因此,开发准确识别剪接位点的有效方法具有重要意义。本文介绍了一种基于支持向量机(SVM)和一种新型马尔可夫链模型DMM2的剪接位点预测算法。与现有的MM1-SVM、Reduced MM1-SVM、SVM-B、LVMM、MM1-RF、MM2F-SVM、MCM-SVM、DM-SVM和DM2-AdaBoost方法相比,该方法有很大的改进。使用重复的10倍交叉验证来评估该方法在HS3D数据集上的性能。此外,我们将其应用于NN269数据集,以检验所提出方法的稳定性。实验结果表明了该方法的可行性和有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A combined SVM and Markov model approach for splice site identification
Due to an exponential increase in biological sequence data, gene detection has become one of the challenging tasks in computational biology. Splice site prediction is an essential part of the gene detection. Thus, it has great significance to develop efficient methods for accurately identifying splice sites. This paper introduces a novel algorithm to predict the splice sites based on support vector machine (SVM) and a new type of Markov chain model, namely DMM2. The proposed method shows great improvement over most of the current state of art methods, including MM1-SVM, Reduced MM1-SVM, SVM-B, LVMM, MM1-RF, MM2F-SVM, MCM-SVM, DM-SVM and DM2-AdaBoost. The repeated 10-fold cross validation was used to assess the performance of the method on the HS3D dataset. In addition, we applied it to NN269 dataset to examine the stability of the proposed method. The experimental results indicate that the new approach is feasible and efficient.
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