基于密码子和支持向量机的基因分类

J. Ma, M. N. Nguyen, G.W.L. Pang, Jagath Rajapakse
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引用次数: 8

摘要

提出了一种新的基因分类方法,采用密码子使用偏向模式作为特征向量,利用支持向量机进行后续分类。首先将给定的DNA序列转换为59维特征向量,每个元素对应于密码子的相对同义使用频率。因此,分类器的输入与DNA序列的大小无关。因此,当待分类的基因长度不同时,我们的方法是有用的,而基于同源性的方法由于难以对不同长度的序列进行比对而不适用。通过对从IMGT/HLA数据库中选择的1841个HLA (Human白细胞抗原)编码序列进行分类,证明了该方法的适用性和实用性。利用密码子使用频率,二元支持向量机将人类MHC(主要组织相容性复合体)分子分为MHC- i和MHC- ii两大类,准确率高达99.30%。采用多类SVM方法对MHC-I类和MHC-II类的子类分类准确率分别达到99.73%和98.38%。结果表明,该方法能够准确地将MHC分子划分为主要类和主要类中的小类。此外,根据密码子使用偏好模式进行基因分类的结果与分子结构和生物学功能一致,进一步验证了我们的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gene Classification using Codon Usage and SVMs
A novel approach for gene classification is proposed, which adopts codon usage bias pattern as feature vector for the subsequent classification using Support Vector Machines (SVMs). A given DNA sequence is first converted to 59-dimensional feature vector, each element corresponding to the relative synonymous usage frequency of a codon. Therefore, the input to the classifier is independent of the size of the DNA sequences. Therefore, our approach is useful when the genes to be classified are of different length, where the homology-based methods are inapplicable due to the difficulty in the alignment of sequences having different lengths. The applicability and usage of the present method is demonstrated by a classification of 1841 HLA (Human Leukocyte Antigen) coding sequences selected from the database of IMGT/HLA. Using the codon usage frequencies, the binary SVM achieved accuracy up to 99.30% for classification human MHC (Major Histocompatibility Complex) molecules in their major classes: MHC-I and MHC-II. By using a multi-class SVM approach, the accuracy rates of 99.73% and 98.38% were achieved for subclasss classification of MHC-I and MHC-II classes, respectively. The results show that the proposed method is capable of accurately classifying MHC molecules in to their major classes as well as in to the subclasses within major classes. Also, the results of gene classification according to the codon usage bias pattern are consistent with the molecule structures and biological functions, further validating our approach.
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