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Prediction of binding peptides to class I Major Histocompatibility Complex using modified scoring matrices and data splitting strategies

机译:使用改进的评分矩阵和数据拆分策略预测与I类主要组织相容性复合物的结合肽

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Predicting peptides that can bind to MHC class I molecules is an important step in the vaccine design process. Computational approaches have potential to provide good predictive models that save both time and cost of the process. Position Specific Scoring Matrix (PSSM) is a reliable approach when dealing with amino acid sequences. PSSM fojination involves carefully selecting its constructing data and parameters. In this work, we apply three different data splitting strategies and propose alternative values for the embedded PSSM parameters. The basic principle of data splitting is to choose train data that is able to represent the whole data. We propose using the Kennard Stone algorithm to highlight the importance of choosing the data constituting the PSSM. Furthermore, this work proposes modifications to PSSM parameters and studies the model behavior in response to each change. The model is applied to experimental data for the Major Histocompatibility Complex of class I. Performance of modified parameters show either comparable or better results to conventional parameters. Moreover, Kennard Stone data splitting algorithm contributed to significant model performance enhancement. (C) 2016 Nakcz Institute of Biocybemetics and Biomedical Engineering of the Polish Academy of Sciences. Published by Elsevier Sp. z o.o. All rights reserved.
机译:预测可与MHC I类分子结合的肽是疫苗设计过程中的重要步骤。计算方法有潜力提供良好的预测模型,从而节省流程时间和成本。特定位置评分矩阵(PSSM)是处理氨基酸序列时的可靠方法。 PSSM整合涉及仔细选择其构造数据和参数。在这项工作中,我们应用了三种不同的数据拆分策略,并为嵌入式PSSM参数提出了替代值。数据拆分的基本原理是选择能够代表整个数据的火车数据。我们建议使用Kennard Stone算法来强调选择构成PSSM的数据的重要性。此外,这项工作提出了对PSSM参数的修改,并研究了响应于每个更改的模型行为。该模型应用于I类主要组织相容性复合物的实验数据。修改后的参数的性能显示出与常规参数相当或更好的结果。此外,肯纳德·斯通(Kennard Stone)的数据分割算法有助于显着提高模型性能。 (C)2016波兰科学院纳克兹生物仿生学和生物医学工程研究所。由Elsevier Sp。发行。动物园。版权所有。

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