Early detection of disease outbreaks and non-outbreaks using incidence data: A framework using feature-based time series classification and machine learning.

IF 3.6 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS PLoS Computational Biology Pub Date : 2025-02-13 eCollection Date: 2025-02-01 DOI:10.1371/journal.pcbi.1012782
Shan Gao, Amit K Chakraborty, Russell Greiner, Mark A Lewis, Hao Wang
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Abstract

Forecasting the occurrence and absence of novel disease outbreaks is essential for disease management, yet existing methods are often context-specific, require a long preparation time, and non-outbreak prediction remains understudied. To address this gap, we propose a novel framework using a feature-based time series classification (TSC) method to forecast outbreaks and non-outbreaks. We tested our methods on synthetic data from a Susceptible-Infected-Recovered (SIR) model for slowly changing, noisy disease dynamics. Outbreak sequences give a transcritical bifurcation within a specified future time window, whereas non-outbreak (null bifurcation) sequences do not. We identified incipient differences, reflected in 22 statistical features and 5 early warning signal indicators, in time series of infectives leading to future outbreaks and non-outbreaks. Classifier performance, given by the area under the receiver-operating curve (AUC), ranged from 0 . 99 for large expanding windows of training data to 0 . 7 for small rolling windows. The framework is further evaluated on four empirical datasets: COVID-19 incidence data from Singapore, 18 other countries, and Edmonton, Canada, as well as SARS data from Hong Kong, with two classifiers exhibiting consistently high accuracy. Our results highlight detectable statistical features distinguishing outbreak and non-outbreak sequences well before potential occurrence, in both synthetic and real-world datasets presented in this study.

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使用发病率数据早期发现疾病爆发和非爆发:使用基于特征的时间序列分类和机器学习的框架。
预测新型疾病暴发的发生和不发生对疾病管理至关重要,然而现有的方法往往是针对具体情况的,需要很长的准备时间,而且对非暴发预测的研究仍然不足。为了解决这一差距,我们提出了一个新的框架,使用基于特征的时间序列分类(TSC)方法来预测爆发和非爆发。我们在一个易感-感染-恢复(SIR)模型的合成数据上测试了我们的方法,该模型用于缓慢变化的嘈杂疾病动态。爆发序列在指定的未来时间窗口内给出跨关键分叉,而非爆发(零分叉)序列则不会。我们在导致未来暴发和非暴发的传染病时间序列中确定了22个统计特征和5个早期预警信号指标所反映的早期差异。分类器的性能,由接受者工作曲线下的面积(AUC)给出,范围从0。99对于训练数据的大规模扩展窗口为0。7适用于小型卷帘窗。该框架在四个经验数据集上进一步进行了评估:来自新加坡、其他18个国家和加拿大埃德蒙顿的COVID-19发病率数据,以及来自香港的SARS数据,其中两个分类器始终表现出较高的准确性。我们的研究结果突出了在本研究中提出的合成数据集和实际数据集中,早在潜在发生之前就区分爆发和非爆发序列的可检测的统计特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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