Group testing with a dilution effect

DOI10.1093/BIOMET/63.3.671MaRDI QIDQ4104786zbMATH OpenOpenAlexFDO

Authors Frank K. Hwang

Publication date 1976

Published in Biometrika (Search for Journal in Brave)

Full work available at URL https://doi.org/10.1093/biomet/63.3.671

Mathematics Subject Classification ID

Parametric hypothesis testing (62F03) Applications of statistics to biology and medical sciences; meta analysis (62P10)

Cited in

(23)

• Optimal configuration of a square array group testing algorithm
• Dual estimation of prevalence and disease incidence in pool-testing strategy
• Randomized-sequential group testing procedures
• Extensions of Dorfman's theory
• Analysis of Multistage Pooling Studies of Biological Specimens for Estimating Disease Incidence and Prevalence
• Sequential classification on lattices with experiment-specific response distributions
• Known mean, unknown maxima? Testing the maximum knowing only the mean
• Nonparametric estimation of distributions and diagnostic accuracy based on group‐tested results with differential misclassification
• Modeling and computation of multistep batch testing for infectious diseases
• The efficient design of Nested Group Testing algorithms for disease identification in clustered data
• Optimal Dorfman group testing for symmetric distributions
• Incorporating retesting outcomes for estimation of disease prevalence
• Is group testing ready for prime-time in disease identification?
• Discussion on: ``Is group testing ready for prime-time in disease identification?
• Prevalence estimation subject to misclassification: the mis-substitution bias and some remedies
• Residual risk and waste in donated blood with pooled nucleic acid testing
• Group testing regression models with dilution submodels
• Optimality of group testing with differential misclassification
• Grouping methods for estimating the prevalences of rare traits from complex survey data that preserve confidentiality of respondents
• Capturing the dilution effect of risk-based grouping with application to COVID-19 screening
• Combining biomarkers to improve diagnostic accuracy in detecting diseases with group-tested data
• Hypergeometric and binomial group sampling with an imperfect test
• Array-based schemes for group screening with test errors which incorporate a concentration effect

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