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A Pan-Specific GRU-Based Recurrent Neural Network for Predicting HLA-I-Binding Peptides

机译:基于泛菌的GRU的复发性神经网络,用于预测HLA-I结合肽

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Human leukocyte antigens (HLAs) play a critical role in human-acquired immune responses by the recognition of non-self-peptides derived from exogenous bacteria, fungi, virus, and so forth. The accurate prediction of HLA-binding peptides is thus extremely useful for the mechanistic research of cell-mediated immunity and related epitope-based vaccine design. In this work, a simple pan-specific gated recurrent unit (GRU)-based recurrent neural network model was successfully proposed for predicting HLA-I-binding peptides. In comparison with the available six allele-specific, four pan-specific, and two ensemble-based prediction models, the GRU model achieves the highest area under the receiver operating characteristic curve (AUC) scores for 21 of 64 entries of the test benchmark datasets. Besides, the GRU model also achieves satisfactory performance on other 24 entries, of which the AUC scores differ by less than 0.1 from the highest scores. Overall, taking the advantages of the GRU network and auto-embedding techniques into account, the established pan-specific GRU model is more simple and direct and shows satisfactory prediction performance for HLA-I-binding peptides with varying lengths.
机译:人的白细胞抗原(HLA)通过识别来自外源细菌,真菌,病毒等的非自肽,在人类获得的免疫反应中起着关键作用。因此,HLA结合肽的精确预测对于细胞介导的免疫和相关表位的疫苗设计非常有用。在这项工作中,成功地提出了一种简单的泛特异性门控复发单元(GRU)基础的复发性神经网络模型,用于预测HLA-I结合肽。与可用的六个等位基因特异性的四个泛特特异性和两个基于组合的预测模型相比,GRU模型在接收器操作特性曲线(AUC)分数下的最高面积为测试基准数据集的64个条目中的21个分数。此外,GRU模型还在其他24个条目上实现了令人满意的性能,其中AUC得分在最高分数中的分数差异小于0.1。总的来说,采取GRU网络的优点和考虑到的自动嵌入技术,所建立的泛特异性GRU模型更加简单,直接,并且对具有不同长度的HLA-I结合肽显示出令人满意的预测性能。

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