利用深度自动编码器进行异常检测,预测 SARS-CoV-2 株系的优势。

IF 6.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Simone Rancati, Giovanna Nicora, Mattia Prosperi, Riccardo Bellazzi, Marco Salemi, Simone Marini
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引用次数: 0

摘要

在 COVID-19 大流行中,新的 SARS-CoV-2 变异株、系和亚系相继出现,它们在很大程度上由于传播性增强和免疫逃逸等因素而取代了早期的毒株。我们提出了一种无监督深度学习异常检测系统 DeepAutoCoV,用于预测未来的优势毒株(FDLs)。我们将 FDLs 定义为病毒(亚)品系,它们将在特定一周内占到 GISAID(支持病毒基因序列共享的公共数据库)中所有病毒序列的 >10%。DeepAutoCoV 是通过对全球和特定国家的数据集进行训练和验证的,这些数据集来自约 4 年时间里采样的 1600 多万个穗状病毒蛋白质序列。DeepAutoCoV 以极低的频率(0.01%-3%)成功标记了 FDL,中位前置时间为 4-17 周,预测 FDL 的效果比基线方法好 5-25 倍。例如,当 B.1.617.2 疫苗参考毒株的频率仅为 0.01% 时,它就被标记为 FDL,这比 COVID-19 更新疫苗考虑该毒株的频率早了一年多。此外,DeepAutoCoV 还能精确定位可能与适应性增强有关的特定突变,从而输出可解释的结果,并为优化公共卫生 "先发制人 "干预策略提供重要启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Forecasting dominance of SARS-CoV-2 lineages by anomaly detection using deep AutoEncoders.

The COVID-19 pandemic is marked by the successive emergence of new SARS-CoV-2 variants, lineages, and sublineages that outcompete earlier strains, largely due to factors like increased transmissibility and immune escape. We propose DeepAutoCoV, an unsupervised deep learning anomaly detection system, to predict future dominant lineages (FDLs). We define FDLs as viral (sub)lineages that will constitute >10% of all the viral sequences added to the GISAID, a public database supporting viral genetic sequence sharing, in a given week. DeepAutoCoV is trained and validated by assembling global and country-specific data sets from over 16 million Spike protein sequences sampled over a period of ~4 years. DeepAutoCoV successfully flags FDLs at very low frequencies (0.01%-3%), with median lead times of 4-17 weeks, and predicts FDLs between ~5 and ~25 times better than a baseline approach. For example, the B.1.617.2 vaccine reference strain was flagged as FDL when its frequency was only 0.01%, more than a year before it was considered for an updated COVID-19 vaccine. Furthermore, DeepAutoCoV outputs interpretable results by pinpointing specific mutations potentially linked to increased fitness and may provide significant insights for the optimization of public health 'pre-emptive' intervention strategies.

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来源期刊
Briefings in bioinformatics
Briefings in bioinformatics 生物-生化研究方法
CiteScore
13.20
自引率
13.70%
发文量
549
审稿时长
6 months
期刊介绍: Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data. The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.
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