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使用逆二项式合并检测估计疾病患病率。

Estimating Disease Prevalence Using Inverse Binomial Pooled Testing.

作者信息

Pritchard Nicholas A, Tebbs Joshua M

机构信息

Department of Mathematics and Statistics, Coastal Carolina University, Conway, SC 29528, USA.

出版信息

J Agric Biol Environ Stat. 2011 Mar 1;16(1):70-87. doi: 10.1007/s13253-010-0036-4.

Abstract

Monitoring populations of hosts as well as insect vectors is an important part of agricultural and public health risk assessment. In applications where pathogen prevalence is likely low, it is common to test pools of subjects for the presence of infection, rather than to test subjects individually. This technique is known as pooled (group) testing. In this paper, we revisit the problem of estimating the population prevalence p from pooled testing, but we consider applications where inverse binomial sampling is used. Our work is unlike previous research in pooled testing, which has largely assumed a binomial model. Inverse sampling is natural to implement when there is a need to report estimates early on in the data collection process and has been used in individual testing applications when disease incidence is low. We consider point and interval estimation procedures for p in this new pooled testing setting, and we use example data sets from the literature to describe and to illustrate our methods.

摘要

监测宿主种群以及昆虫媒介是农业和公共卫生风险评估的重要组成部分。在病原体流行率可能较低的应用中,通常会对样本池进行感染检测,而不是对个体进行检测。这种技术被称为混合(分组)检测。在本文中,我们重新审视了从混合检测中估计总体流行率p的问题,但我们考虑的是使用逆二项抽样的应用。我们的工作不同于以往关于混合检测的研究,以往研究大多假设为二项模型。当需要在数据收集过程早期报告估计值时,逆抽样很容易实施,并且在疾病发病率较低的个体检测应用中也有使用。我们考虑了在这种新的混合检测设置下p的点估计和区间估计程序,并使用文献中的示例数据集来描述和说明我们的方法。

相似文献

1
Estimating Disease Prevalence Using Inverse Binomial Pooled Testing.使用逆二项式合并检测估计疾病患病率。
J Agric Biol Environ Stat. 2011 Mar 1;16(1):70-87. doi: 10.1007/s13253-010-0036-4.
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Inverse sampling regression for pooled data.合并数据的逆抽样回归
Stat Methods Med Res. 2017 Jun;26(3):1093-1109. doi: 10.1177/0962280214568047. Epub 2015 Jan 19.

本文引用的文献

2
On a method of estimating frequencies.论一种估计频率的方法。
Biometrika. 1945 Nov;33:222-5. doi: 10.1093/biomet/33.3.222.

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