Scoring epidemiological forecasts on transformed scales.

IF 4.3 2区 生物学
PLoS Computational Biology Pub Date : 2023-08-29 eCollection Date: 2023-08-01 DOI:10.1371/journal.pcbi.1011393
Nikos I Bosse, Sam Abbott, Anne Cori, Edwin van Leeuwen, Johannes Bracher, Sebastian Funk
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引用次数: 0

Abstract

Forecast evaluation is essential for the development of predictive epidemic models and can inform their use for public health decision-making. Common scores to evaluate epidemiological forecasts are the Continuous Ranked Probability Score (CRPS) and the Weighted Interval Score (WIS), which can be seen as measures of the absolute distance between the forecast distribution and the observation. However, applying these scores directly to predicted and observed incidence counts may not be the most appropriate due to the exponential nature of epidemic processes and the varying magnitudes of observed values across space and time. In this paper, we argue that transforming counts before applying scores such as the CRPS or WIS can effectively mitigate these difficulties and yield epidemiologically meaningful and easily interpretable results. Using the CRPS on log-transformed values as an example, we list three attractive properties: Firstly, it can be interpreted as a probabilistic version of a relative error. Secondly, it reflects how well models predicted the time-varying epidemic growth rate. And lastly, using arguments on variance-stabilizing transformations, it can be shown that under the assumption of a quadratic mean-variance relationship, the logarithmic transformation leads to expected CRPS values which are independent of the order of magnitude of the predicted quantity. Applying a transformation of log(x + 1) to data and forecasts from the European COVID-19 Forecast Hub, we find that it changes model rankings regardless of stratification by forecast date, location or target types. Situations in which models missed the beginning of upward swings are more strongly emphasised while failing to predict a downturn following a peak is less severely penalised when scoring transformed forecasts as opposed to untransformed ones. We conclude that appropriate transformations, of which the natural logarithm is only one particularly attractive option, should be considered when assessing the performance of different models in the context of infectious disease incidence.

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在转换后的量表上对流行病学预测进行评分。
预测评估对于开发流行病预测模型至关重要,可以为公共卫生决策提供信息。评估流行病学预测的常见分数是连续排序概率分数(CRPS)和加权区间分数(WIS),它们可以被视为预测分布和观测之间绝对距离的度量。然而,由于流行病过程的指数性质以及观察值在空间和时间上的变化幅度,将这些分数直接应用于预测和观察到的发病率可能不是最合适的。在本文中,我们认为,在应用CRPS或WIS等评分之前转换计数可以有效地缓解这些困难,并产生具有流行病学意义且易于解释的结果。以对数变换值上的CRPS为例,我们列出了三个有吸引力的性质:首先,它可以被解释为相对误差的概率版本。其次,它反映了模型对时变流行病增长率的预测效果。最后,利用方差稳定变换的自变量,可以表明,在二次均方差关系的假设下,对数变换产生的预期CRPS值与预测量的数量级无关。将log(x+1)转换应用于欧洲新冠肺炎预测中心的数据和预测,我们发现无论预测日期、地点或目标类型如何分层,它都会改变模型排名。模型错过了向上波动开始的情况得到了更有力的强调,而在对转换后的预测进行评分时,与未转换的预测相比,未能预测峰值后的衰退受到的惩罚较小。我们得出的结论是,在评估传染病发病率背景下不同模型的性能时,应该考虑适当的转换,自然对数只是其中一个特别有吸引力的选择。
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 生物-生化研究方法
CiteScore
7.10
自引率
4.70%
发文量
820
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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