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本文引用的文献

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Attenuation of Influenza A Virus Disease Severity by Viral Coinfection in a Mouse Model.病毒混合感染对小鼠流感病毒病严重程度的抑制作用。
J Virol. 2018 Nov 12;92(23). doi: 10.1128/JVI.00881-18. Print 2018 Dec 1.
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SLDAssay: A software package and web tool for analyzing limiting dilution assays.SLD分析:一个用于分析有限稀释分析的软件包和网络工具。
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Vector-Borne Pathogen and Host Evolution in a Structured Immuno-Epidemiological System.结构化免疫-流行病学系统中的媒介传播病原体与宿主进化
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Designing and Interpreting Limiting Dilution Assays: General Principles and Applications to the Latent Reservoir for Human Immunodeficiency Virus-1.设计和解释有限稀释分析:一般原理及其在人类免疫缺陷病毒-1潜伏库中的应用。
Open Forum Infect Dis. 2015 Aug 26;2(4):ofv123. doi: 10.1093/ofid/ofv123. eCollection 2015 Dec.
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From evidence to understanding: a commentary on Fisher (1922) 'On the mathematical foundations of theoretical statistics'.从证据到理解:对费希尔(1922年)《论理论统计学的数学基础》的评论
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Infectivity assays of human rhinovirus-A and -B serotypes.人鼻病毒A和B血清型的感染性测定。
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The estimation of bacterial densities from dilution series.通过稀释系列估算细菌密度。
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On the Statistical Interpretation of some Bacteriological Methods employed in Water Analysis.关于水分析中某些细菌学方法的统计学解释。
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Statistical design for a small serial dilution series.小系列连续稀释的统计设计。
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10
ELDA: extreme limiting dilution analysis for comparing depleted and enriched populations in stem cell and other assays.ELDA:用于在干细胞及其他检测中比较耗尽和富集群体的极限稀释分析。
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用于稀释试验的两阶段实验设计。

A two-stage experimental design for dilution assays.

作者信息

Ferguson Jake M, Miura Tanya A, Miller Craig R

机构信息

Center for Modeling Complex Interactions, University of Idaho, Moscow, Idaho.

Current address: Department of Biology, University of Hawai'i at Mānoa, Honolulu, Hawai'i.

出版信息

Biometrics. 2019 Sep;75(3):1009-1016. doi: 10.1111/biom.13032. Epub 2019 Apr 3.

DOI:10.1111/biom.13032
PMID:30690720
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7199778/
Abstract

Dilution assays to determine solute concentration have found wide use in biomedical research. Many dilution assays return imprecise concentration estimates because they are only done to orders of magnitude. Previous statistical work has focused on how to design efficient experiments that can return more precise estimates, however this work has not considered the practical difficulties of implementing these designs in the laboratory. We developed a two-stage experiment with a first stage that obtains an order of magnitude estimate and a second stage that concentrates effort on the most informative dilution to increase estimator precision. We show using simulations and an empirical example that the best two-stage experimental designs yield estimates that are remarkably more accurate than standard methods with equivalent effort. This work demonstrates how to utilize previous advances in experimental design in a manner consistent with current laboratory practice. We expect that multi-stage designs will prove to be useful for obtaining precise estimates with minimal experimental effort.

摘要

用于确定溶质浓度的稀释试验在生物医学研究中得到了广泛应用。许多稀释试验返回的浓度估计值不准确,因为它们只做到了数量级。以往的统计工作主要集中在如何设计高效的实验以返回更精确的估计值,然而这项工作并未考虑在实验室中实施这些设计的实际困难。我们开发了一种两阶段实验,第一阶段获得数量级估计值,第二阶段将精力集中在信息量最大的稀释上以提高估计精度。我们通过模拟和一个实证例子表明,最佳的两阶段实验设计所产生的估计值比同等工作量的标准方法要准确得多。这项工作展示了如何以与当前实验室实践相一致的方式利用实验设计的先前进展。我们预计,多阶段设计将被证明对于以最少的实验工作量获得精确估计值是有用的。