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具有均匀混合的非参数序列间隔估计

Nonparametric serial interval estimation with uniform mixtures.

作者信息

Gressani Oswaldo, Hens Niel

机构信息

Interuniversity Institute for Biostatistics and Statistical Bioinformatics (I-BioStat), Data Science Institute, Hasselt University, Hasselt, Belgium.

Centre for Health Economics Research and Modelling Infectious Diseases, Vaxinfectio, University of Antwerp, Antwerp, Belgium.

出版信息

PLoS Comput Biol. 2025 Aug 4;21(8):e1013338. doi: 10.1371/journal.pcbi.1013338. eCollection 2025 Aug.

Abstract

The serial interval of an infectious disease is a key instrument to understand transmission dynamics. Estimation of the serial interval distribution from illness onset data extracted from transmission pairs is challenging due to the presence of censoring and state-of-the-art methods mostly rely on parametric models. We present a fully data-driven methodology to estimate the serial interval distribution based on interval-censored serial interval data. The proposed nonparametric estimator of the cumulative distribution function of the serial interval is based on the class of uniform mixtures. Closed-form solutions are available for point estimates of different serial interval features and the bootstrap is used to construct confidence intervals. Algorithms underlying our approach are simple, stable, and computationally inexpensive, making them easily implementable in a programming language that is most familiar to a potential user. The nonparametric user-friendly routine is included in the EpiDelays package for ease of implementation. Our method complements existing parametric approaches for serial interval estimation and permits to analyze past, current, or future illness onset data streams following a set of best practices in epidemiological delay modeling.

摘要

传染病的传播间隔是了解传播动态的关键工具。由于存在删失情况,从传播对中提取的发病数据估计传播间隔分布具有挑战性,并且现有技术方法大多依赖参数模型。我们提出了一种基于区间删失的传播间隔数据来估计传播间隔分布的完全数据驱动方法。所提出的传播间隔累积分布函数的非参数估计器基于均匀混合类。对于不同传播间隔特征的点估计,有封闭形式的解,并且使用自助法来构建置信区间。我们方法的基础算法简单、稳定且计算成本低,使其易于在潜在用户最熟悉的编程语言中实现。为便于实施,EpiDelays软件包中包含了这个非参数且用户友好的程序。我们的方法补充了现有的传播间隔估计参数方法,并允许按照流行病学延迟建模中的一组最佳实践来分析过去、当前或未来的发病数据流。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06e6/12338840/9d2ab38982f0/pcbi.1013338.g001.jpg

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