Evidence map›Paper›PMID 40084581›Full record

ArticleStatistics in medicine2025

Bayesian Additive Regression Trees for Group Testing Data.

Madeleine E St Ville, Christopher S McMahan, Joe D Bible, Joshua M Tebbs, Christopher R Bilder

Abstract read
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Article in Statistics in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Madeleine E St VilleEunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.ORCID https://orcid.org/0000-0002-9863-9720
Christopher S McMahanSchool of Mathematical and Statistical Sciences, Clemson University, Clemson, SC, USA.ORCID https://orcid.org/0000-0001-5056-9615
Joe D BibleSchool of Mathematical and Statistical Sciences, Clemson University, Clemson, SC, USA.ORCID https://orcid.org/0000-0002-7010-5321
Joshua M TebbsDepartment of Statistics, University of South Carolina, Columbia, SC, USA.ORCID https://orcid.org/0000-0002-6762-7241
Christopher R BilderDepartment of Statistics, University of Nebraska-Lincoln, Lincoln, NE, USA.ORCID https://orcid.org/0000-0002-2848-8576

Funding

Group testing for infectious disease detection: multiplex assays and back-end screeningR01AI121351 · NIAID · UNIVERSITY OF NEBRASKA LINCOLN · PI BILDER, CHRISTOPHER R · 2016 to 2025
$3.3M
National Science Foundation OIA-1826715NIAID NIH HHS R01 AI121351NIH HHS R01 AI121351
6 · The paper itself

Abstract

When screening for low-prevalence diseases, pooling specimens (e.g., blood, urine, swabs, etc.) through group testing has the potential to substantially reduce costs when compared to testing specimens individually. A common goal in group testing applications is to estimate the relationship between an individual's true disease status and their individual-level covariate information. However, estimating such a relationship is a non-trivial problem because true individual disease statuses are unknown due to the group testing protocol and the possibility of imperfect testing. While several regression methods have been developed in recent years to accommodate the complexity of group testing data, the functional form of covariate effects is typically assumed to be known. To avoid model misspecification and to provide a more flexible approach, we propose a Bayesian additive regression trees framework to model the individual-level probability of disease with potentially misclassified group testing data. Our methods can be used to analyze data arising from any group testing protocol with the goal of estimating unknown functions of covariates and assay classification accuracy probabilities.

Indexed as

Computer SimulationModels, StatisticalBayes TheoremHumansRegression Analysisdecision treeslatent variable modelingmachine learningnon‐parametric regressionpooled testing

Identifiers

PMID40084581
PMCPMC11907685

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.