A Hybrid Method of Propensity Scales and Support Vector Machine in a Linear Epitope Prediction

Hsin-Wei Wang, Ya-Chi Lin, Tun-Wen Pai, Pei-Wen Tsai, Hao-Teng Chang
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引用次数: 1

Abstract

An epitope activates B cells to amplify and induce antibodies which can neutralize the foreign molecules, particles and pathogens. It also plays a crucial role in developing synthetic peptides for vaccination. Identification of epitopes using biological screening approaches is time consuming and high cost. Therefore, bioinformatics approaches are developed to enhance the speed of identifying the epitopes and conserve time. Herein, a combinatorial methodology based on physico-chemical properties and SVM (Support Vector Machine) techniques was proposed to address the aim of this study. Datasets of epitope and non epitope segments with 2, 3 and 4 residues in length were trained and applied as statistical features of SVM. After training, three datasets including one curated and two public ones were employed to evaluate the performance of the proposed system which was also compared with four existing LE predictors, BepiPred, ABCpred, BCPred and FBCPred. Our proposed system has presented better specificity, accuracy, and positive prediction value (PPV) in most testing cases. High specificity and PPV of a linear epitope prediction can lead to an efficient and effective design on biological experiments.
倾向尺度与支持向量机混合方法在线性表位预测中的应用
抗原表位激活B细胞扩增和诱导抗体,这些抗体可以中和外来分子、颗粒和病原体。它在开发用于疫苗接种的合成肽方面也起着至关重要的作用。使用生物筛选方法鉴定表位耗时且成本高。因此,开发生物信息学方法来提高识别表位的速度和节省时间。本文提出了一种基于物理化学性质和支持向量机(SVM)技术的组合方法来解决本研究的目的。训练长度分别为2,3和4个残基的表位片段和非表位片段数据集,并将其作为SVM的统计特征。训练后,使用三个数据集(包括一个管理数据集和两个公共数据集)来评估所提出系统的性能,并将其与现有的四个LE预测因子BepiPred, ABCpred, BCPred和FBCPred进行比较。我们的系统在大多数测试案例中具有更好的特异性、准确性和阳性预测值(PPV)。线性表位预测的高特异性和PPV可为生物实验设计提供高效、有效的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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