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Poster: Linear B-cell epitope prediction based on Support Vector Machine and propensity scales

机译:海报:基于支持向量机和倾向量表的线性B细胞表位预测

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B-cell epitopes play an important role for developing synthetic peptide vaccines and inducing antibody responses. Applying biological experiments for epitope identification is time consuming and demands a lot of experimental resources. Nevertheless, it is important yet challenging task for designing a computer-aided B-cell linear epitope prediction system with high precision rates. In this paper, a combinatorial mechanism based on physico-chemical properties and SVM (Support Vector Machine) techniques for linear epitope prediction is proposed. Amino acid segments (AASs) with 2, 3 and 4 residues in length of both epitopes and non-epitopes datasets [1, 2] were trained and applied as statistical features of SVM [3]. The proposed system was evaluated by one curated dataset and two public epitope databases, and its performance was compared with four existing approaches. The experimental results have shown that our proposed method outperforms other existing systems in terms of specificity, accuracy, and positive predictive value in most testing cases. Besides, the sensitivity is also achieved with a comparable performance.
机译:B细胞表位在开发合成肽疫苗和诱导抗体反应中起重要作用。将生物学实验用于表位鉴定是耗时的并且需要大量实验资源。然而,设计具有高精度的计算机辅助B细胞线性抗原决定簇预测系统是一项重要而又具有挑战性的任务。本文提出了一种基于理化性质和支持向量机(SVM)的线性表位预测组合机制。对表位和非表位数据集[1、2]的长度分别为2、3和4个残基的氨基酸片段(AAS)进行了训练,并将其用作SVM的统计特征[3]。该系统通过一个策展数据集和两个公共表位数据库进行了评估,并将其性能与四种现有方法进行了比较。实验结果表明,在大多数测试案例中,我们提出的方法在特异性,准确性和阳性预测值方面均优于其他现有系统。此外,灵敏度也达到了可比的性能。

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