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DOI 10.1093/biostatistics/kxy058

Медицинская библиотека · Biostatistics (Oxford, England) · 2020

Array testing for multiplex assays.

Hou Peijie, Tebbs Joshua M, Wang Dewei, McMahan Christopher S, Bilder Christopher R

СтатьяПоддержка NIH: внешняя программаПеревод в очереди

Аннотация

Group testing involves pooling individual specimens (e.g., blood, urine, swabs, etc.) and testing the pools for the presence of disease. When the proportion of diseased individuals is small, group testing can greatly reduce the number of tests needed to screen a population. Statistical research in group testing has traditionally focused on applications for a single disease. However, blood service organizations and large-scale disease surveillance programs are increasingly moving towards the use of multiplex assays, which measure multiple disease biomarkers at once. Tebbs and others (2013, Two-stage hierarchical group testing for multiple infections with application to the Infertility Prevention Project. Biometrics69, 1064-1073) and Hou and others (2017, Hierarchical group testing for multiple infections. Biometrics73, 656-665) were the first to examine hierarchical group testing case identification procedures for multiple diseases. In this article, we propose new non-hierarchical procedures which utilize two-dimensional arrays. We derive closed-form expressions for the expected number of tests per individual and classification accuracy probabilities and show that array testing can be more efficient than hierarchical procedures when screening individuals for multiple diseases at once. We illustrate the potential of using array testing in the detection of chlamydia and gonorrhea for a statewide screening program in Iowa. Finally, we describe an R/Shiny application that will help practitioners identify the best multiple-disease case identification algorithm.

Для цитирования: Hou Peijie, Tebbs Joshua M, Wang Dewei, McMahan Christopher S, Bilder Christopher R. Array testing for multiplex assays.. Biostatistics (Oxford, England). 2020. DOI: 10.1093/biostatistics/kxy058.

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