Group testing with a new goal, estimation

DOI10.1093/BIOMET/62.1.181MaRDI QIDQ4066454zbMATH OpenOpenAlexWikidataFDO

Authors Milton Sobel, Robert M. Elashoff

Publication date 1975

Published in Biometrika (Search for Journal in Brave)

Full work available at URL http://hdl.handle.net/11299/199154

Mathematics Subject Classification ID

Design of statistical experiments (62K99) Applications of statistics in engineering and industry; control charts (62P30)

Cited in

(23)

• Confidence intervals for the difference of two proportions estimated from pooled samples
• Robust procedures for experimental design in group testing considering misclassification
• Dual estimation of prevalence and disease incidence in pool-testing strategy
• Multistage Group Testing Procedure (Group Screening)
• Randomized-sequential group testing procedures
• Statistical Inference Based on Pooled Data: A Moment-Based Estimating Equation Approach
• Sequential estimation in the group testing problem
• Extensions of Dorfman's theory
• Analysis of Multistage Pooling Studies of Biological Specimens for Estimating Disease Incidence and Prevalence
• Using Pooled Exposure Assessment to Improve Efficiency in Case‐Control Studies
• Group testing regression model estimation when case identification is a goal
• Estimating proportions by group retesting with unequal group sizes at each stage
• Estimation of proportions by group testing with retesting of positive groups
• Group Testing with a Goal in Estimating the Number of Defects Under Imperfect Environmental Stress Screen Levels
• Known mean, unknown maxima? Testing the maximum knowing only the mean
• Optimal Dorfman group testing for symmetric distributions
• Incorporating retesting outcomes for estimation of disease prevalence
• Survival analysis under the Cox proportional hazards model with pooled covariates
• Prevalence estimation subject to misclassification: the mis-substitution bias and some remedies
• Optimality of group testing with differential misclassification
• Sequential prevalence estimation with pooling and continuous test outcomes
• Grouping methods for estimating the prevalences of rare traits from complex survey data that preserve confidentiality of respondents
• Combining biomarkers to improve diagnostic accuracy in detecting diseases with group-tested data

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