Christopher S McMahan, Chase N Joyner, Joshua M Tebbs, Christopher R Bilder
{"title":"A mixed-effects Bayesian regression model for multivariate group testing data.","authors":"Christopher S McMahan, Chase N Joyner, Joshua M Tebbs, Christopher R Bilder","doi":"10.1093/biomtc/ujaf028","DOIUrl":null,"url":null,"abstract":"<p><p>Laboratories use group (pooled) testing with multiplex assays to reduce the time and cost associated with screening large populations for infectious diseases. Multiplex assays test for multiple diseases simultaneously, and combining their use with group testing can lead to highly efficient screening protocols. However, these benefits come at the expense of a more complex data structure which can hinder surveillance efforts. To overcome this challenge, we develop a general Bayesian framework to estimate a mixed multivariate probit model with data arising from any group testing protocol that uses multiplex assays. In the formulation of this model, we account for the correlation between true disease statuses and heterogeneity across population subgroups, and we provide for automated variable selection through the adoption of spike and slab priors. To perform model fitting, we develop an attractive posterior sampling algorithm which is straightforward to implement. We illustrate our methodology through numerical studies and analyze chlamydia and gonorrhea group testing data collected by the State Hygienic Laboratory at the University of Iowa.</p>","PeriodicalId":8930,"journal":{"name":"Biometrics","volume":"81 1","pages":""},"PeriodicalIF":1.4000,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11926587/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biometrics","FirstCategoryId":"100","ListUrlMain":"https://doi.org/10.1093/biomtc/ujaf028","RegionNum":4,"RegionCategory":"数学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Laboratories use group (pooled) testing with multiplex assays to reduce the time and cost associated with screening large populations for infectious diseases. Multiplex assays test for multiple diseases simultaneously, and combining their use with group testing can lead to highly efficient screening protocols. However, these benefits come at the expense of a more complex data structure which can hinder surveillance efforts. To overcome this challenge, we develop a general Bayesian framework to estimate a mixed multivariate probit model with data arising from any group testing protocol that uses multiplex assays. In the formulation of this model, we account for the correlation between true disease statuses and heterogeneity across population subgroups, and we provide for automated variable selection through the adoption of spike and slab priors. To perform model fitting, we develop an attractive posterior sampling algorithm which is straightforward to implement. We illustrate our methodology through numerical studies and analyze chlamydia and gonorrhea group testing data collected by the State Hygienic Laboratory at the University of Iowa.
期刊介绍:
The International Biometric Society is an international society promoting the development and application of statistical and mathematical theory and methods in the biosciences, including agriculture, biomedical science and public health, ecology, environmental sciences, forestry, and allied disciplines. The Society welcomes as members statisticians, mathematicians, biological scientists, and others devoted to interdisciplinary efforts in advancing the collection and interpretation of information in the biosciences. The Society sponsors the biennial International Biometric Conference, held in sites throughout the world; through its National Groups and Regions, it also Society sponsors regional and local meetings.