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Predicting MHC class I binder: existing approaches and a novel recurrent neural network solution.预测 MHC Ⅰ类结合肽:现有方法和一种新的递归神经网络解决方案。
Brief Bioinform. 2021 Nov 5;22(6). doi: 10.1093/bib/bbab216.
2
MHCflurry 2.0: Improved Pan-Allele Prediction of MHC Class I-Presented Peptides by Incorporating Antigen Processing.MHCflurry 2.0:通过纳入抗原加工提高 MHC I 类呈递肽的泛等位基因预测。
Cell Syst. 2020 Jul 22;11(1):42-48.e7. doi: 10.1016/j.cels.2020.06.010. Epub 2020 Jul 14.
3
T Cell Epitope Predictions.T 细胞表位预测。
Annu Rev Immunol. 2020 Apr 26;38:123-145. doi: 10.1146/annurev-immunol-082119-124838. Epub 2020 Feb 11.
4
A comprehensive review and performance evaluation of bioinformatics tools for HLA class I peptide-binding prediction.HLA 类 I 肽结合预测的生物信息学工具的综合评价与性能评估。
Brief Bioinform. 2020 Jul 15;21(4):1119-1135. doi: 10.1093/bib/bbz051.
5
Performance Evaluation of MHC Class-I Binding Prediction Tools Based on an Experimentally Validated MHC-Peptide Binding Data Set.基于实验验证的 MHC-肽结合数据集的 MHC 类 I 结合预测工具的性能评估。
Cancer Immunol Res. 2019 May;7(5):719-736. doi: 10.1158/2326-6066.CIR-18-0584. Epub 2019 Mar 22.
6
DeepSeqPan, a novel deep convolutional neural network model for pan-specific class I HLA-peptide binding affinity prediction.DeepSeqPan,一种新的深度卷积神经网络模型,用于 pan 特异性 class I HLA-肽结合亲和力预测。
Sci Rep. 2019 Jan 28;9(1):794. doi: 10.1038/s41598-018-37214-1.
7
Systematically benchmarking peptide-MHC binding predictors: From synthetic to naturally processed epitopes.系统地对肽-MHC 结合预测因子进行基准测试:从合成到天然加工的表位。
PLoS Comput Biol. 2018 Nov 8;14(11):e1006457. doi: 10.1371/journal.pcbi.1006457. eCollection 2018 Nov.
8
NetMHCpan-4.0: Improved Peptide-MHC Class I Interaction Predictions Integrating Eluted Ligand and Peptide Binding Affinity Data.NetMHCpan-4.0:整合洗脱配体和肽结合亲和力数据的改进的肽与主要组织相容性复合体I类相互作用预测
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9
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IEDB MHC 类 I 自动化基准的全面分析。

A comprehensive analysis of the IEDB MHC class-I automated benchmark.

机构信息

Division of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, California 92037, USA.

Fiocruz Ceará, Fundação Oswaldo Cruz, Rua São José s/n, Precabura, Eusébio/CE, Brazil.

出版信息

Brief Bioinform. 2022 Jul 18;23(4). doi: 10.1093/bib/bbac259.

DOI:10.1093/bib/bbac259
PMID:35794711
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9618166/
Abstract

In 2014, the Immune Epitope Database automated benchmark was created to compare the performance of the MHC class I binding predictors. However, this is not a straightforward process due to the different and non-standardized outputs of the methods. Additionally, some methods are more restrictive regarding the HLA alleles and epitope sizes for which they predict binding affinities, while others are more comprehensive. To address how these problems impacted the ranking of the predictors, we developed an approach to assess the reliability of different metrics. We found that using percentile-ranked results improved the stability of the ranks and allowed the predictors to be reliably ranked despite not being evaluated on the same data. We also found that given the rate new data are incorporated into the benchmark, a new method must wait for at least 4 years to be ranked against the pre-existing methods. The best-performing tools with statistically indistinguishable scores in this benchmark were NetMHCcons, NetMHCpan4.0, ANN3.4, NetMHCpan3.0 and NetMHCpan2.8. The results of this study will be used to improve the evaluation and display of benchmark performance. We highly encourage anyone working on MHC binding predictions to participate in this benchmark to get an unbiased evaluation of their predictors.

摘要

2014 年,创建了免疫表位数据库自动化基准测试,以比较 MHC Ⅰ类结合预测器的性能。然而,由于方法的不同和非标准化输出,这并非易事。此外,一些方法对其预测结合亲和力的 HLA 等位基因和表位大小的限制较多,而另一些方法则更为全面。为了解决这些问题如何影响预测器的排名,我们开发了一种评估不同指标可靠性的方法。我们发现,使用百分位排名结果可以提高排名的稳定性,并允许即使不在相同数据上进行评估,也能可靠地对预测器进行排名。我们还发现,鉴于新数据纳入基准的速度,新方法必须等待至少 4 年才能与现有的方法进行排名。在该基准中表现最佳且得分统计学上无法区分的工具是 NetMHCcons、NetMHCpan4.0、ANN3.4、NetMHCpan3.0 和 NetMHCpan2.8。本研究的结果将用于改进基准性能的评估和展示。我们强烈鼓励从事 MHC 结合预测的任何人参与该基准测试,以对其预测器进行公正的评估。