Cargando…
Misclassified group-tested current status data
Group testing, introduced by Dorfman (1943), has been used to reduce costs when estimating the prevalence of a binary characteristic based on a screening test of [Formula: see text] groups that include [Formula: see text] independent individuals in total. If the unknown prevalence is low and the scr...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793678/ https://www.ncbi.nlm.nih.gov/pubmed/29422690 http://dx.doi.org/10.1093/biomet/asw043 |
_version_ | 1783297007465529344 |
---|---|
author | Petito, L. C. Jewell, N. P. |
author_facet | Petito, L. C. Jewell, N. P. |
author_sort | Petito, L. C. |
collection | PubMed |
description | Group testing, introduced by Dorfman (1943), has been used to reduce costs when estimating the prevalence of a binary characteristic based on a screening test of [Formula: see text] groups that include [Formula: see text] independent individuals in total. If the unknown prevalence is low and the screening test suffers from misclassification, it is also possible to obtain more precise prevalence estimates than those obtained from testing all [Formula: see text] samples separately (Tu et al., 1994). In some applications, the individual binary response corresponds to whether an underlying time-to-event variable [Formula: see text] is less than an observed screening time [Formula: see text] , a data structure known as current status data. Given sufficient variation in the observed [Formula: see text] values, it is possible to estimate the distribution function [Formula: see text] of [Formula: see text] nonparametrically, at least at some points in its support, using the pool-adjacent-violators algorithm (Ayer et al., 1955). Here, we consider nonparametric estimation of [Formula: see text] based on group-tested current status data for groups of size [Formula: see text] where the group tests positive if and only if any individual’s unobserved [Formula: see text] is less than the corresponding observed [Formula: see text]. We investigate the performance of the group-based estimator as compared to the individual test nonparametric maximum likelihood estimator, and show that the former can be more precise in the presence of misclassification for low values of [Formula: see text]. Potential applications include testing for the presence of various diseases in pooled samples where interest focuses on the age-at-incidence distribution rather than overall prevalence. We apply this estimator to the age-at-incidence curve for hepatitis C infection in a sample of U.S. women who gave birth to a child in 2014, where group assignment is done at random and based on maternal age. We discuss connections to other work in the literature, as well as potential extensions. |
format | Online Article Text |
id | pubmed-5793678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57936782018-02-06 Misclassified group-tested current status data Petito, L. C. Jewell, N. P. Biometrika Articles Group testing, introduced by Dorfman (1943), has been used to reduce costs when estimating the prevalence of a binary characteristic based on a screening test of [Formula: see text] groups that include [Formula: see text] independent individuals in total. If the unknown prevalence is low and the screening test suffers from misclassification, it is also possible to obtain more precise prevalence estimates than those obtained from testing all [Formula: see text] samples separately (Tu et al., 1994). In some applications, the individual binary response corresponds to whether an underlying time-to-event variable [Formula: see text] is less than an observed screening time [Formula: see text] , a data structure known as current status data. Given sufficient variation in the observed [Formula: see text] values, it is possible to estimate the distribution function [Formula: see text] of [Formula: see text] nonparametrically, at least at some points in its support, using the pool-adjacent-violators algorithm (Ayer et al., 1955). Here, we consider nonparametric estimation of [Formula: see text] based on group-tested current status data for groups of size [Formula: see text] where the group tests positive if and only if any individual’s unobserved [Formula: see text] is less than the corresponding observed [Formula: see text]. We investigate the performance of the group-based estimator as compared to the individual test nonparametric maximum likelihood estimator, and show that the former can be more precise in the presence of misclassification for low values of [Formula: see text]. Potential applications include testing for the presence of various diseases in pooled samples where interest focuses on the age-at-incidence distribution rather than overall prevalence. We apply this estimator to the age-at-incidence curve for hepatitis C infection in a sample of U.S. women who gave birth to a child in 2014, where group assignment is done at random and based on maternal age. We discuss connections to other work in the literature, as well as potential extensions. Oxford University Press 2016-12 2016-12-08 /pmc/articles/PMC5793678/ /pubmed/29422690 http://dx.doi.org/10.1093/biomet/asw043 Text en © 2016 Biometrika Trust |
spellingShingle | Articles Petito, L. C. Jewell, N. P. Misclassified group-tested current status data |
title | Misclassified group-tested current status data |
title_full | Misclassified group-tested current status data |
title_fullStr | Misclassified group-tested current status data |
title_full_unstemmed | Misclassified group-tested current status data |
title_short | Misclassified group-tested current status data |
title_sort | misclassified group-tested current status data |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793678/ https://www.ncbi.nlm.nih.gov/pubmed/29422690 http://dx.doi.org/10.1093/biomet/asw043 |
work_keys_str_mv | AT petitolc misclassifiedgrouptestedcurrentstatusdata AT jewellnp misclassifiedgrouptestedcurrentstatusdata |