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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尺度的线性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细胞表位对开发合成肽疫苗和诱导抗体反应发挥着重要作用。应用表位识别的生物实验是耗时和要求大量的实验资源。尽管如此,对于设计具有高精度速率的计算机辅助B细胞线性表位预测系统是重要的,具体而具有挑战性的任务。本文提出了一种基于物理化学性质和SVM(支持向量机)的线性表位预测技术的组合机构。培训并施加2,3和4个残留物的氨基酸段(AASS),其长度和非表位数据集[1,2]培训并施加为SVM的统计特征[3]。所提出的系统由一个策划数据集和两种公共表位数据库评估,其性能与四种现有方法进行了比较。实验结果表明,我们所提出的方法在大多数测试用例中以特异性,准确性和阳性预测值表现出其他现有系统。此外,还以可比性的性能实现了灵敏度。

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