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Spatial heterogeneity of type I error for local cluster detection tests
BACKGROUND: Just as power, type I error of cluster detection tests (CDTs) should be spatially assessed. Indeed, CDTs’ type I error and power have both a spatial component as CDTs both detect and locate clusters. In the case of type I error, the spatial distribution of wrongly detected clusters (WDCs...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4040115/ https://www.ncbi.nlm.nih.gov/pubmed/24885343 http://dx.doi.org/10.1186/1476-072X-13-15 |
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author | Guttmann, Aline Li, Xinran Gaudart, Jean Gérard, Yan Demongeot, Jacques Boire, Jean-Yves Ouchchane, Lemlih |
author_facet | Guttmann, Aline Li, Xinran Gaudart, Jean Gérard, Yan Demongeot, Jacques Boire, Jean-Yves Ouchchane, Lemlih |
author_sort | Guttmann, Aline |
collection | PubMed |
description | BACKGROUND: Just as power, type I error of cluster detection tests (CDTs) should be spatially assessed. Indeed, CDTs’ type I error and power have both a spatial component as CDTs both detect and locate clusters. In the case of type I error, the spatial distribution of wrongly detected clusters (WDCs) can be particularly affected by edge effect. This simulation study aims to describe the spatial distribution of WDCs and to confirm and quantify the presence of edge effect. METHODS: A simulation of 40 000 datasets has been performed under the null hypothesis of risk homogeneity. The simulation design used realistic parameters from survey data on birth defects, and in particular, two baseline risks. The simulated datasets were analyzed using the Kulldorff’s spatial scan as a commonly used test whose behavior is otherwise well known. To describe the spatial distribution of type I error, we defined the participation rate for each spatial unit of the region. We used this indicator in a new statistical test proposed to confirm, as well as quantify, the edge effect. RESULTS: The predefined type I error of 5% was respected for both baseline risks. Results showed strong edge effect in participation rates, with a descending gradient from center to edge, and WDCs more often centrally situated. CONCLUSIONS: In routine analysis of real data, clusters on the edge of the region should be carefully considered as they rarely occur when there is no cluster. Further work is needed to combine results from power studies with this work in order to optimize CDTs performance. |
format | Online Article Text |
id | pubmed-4040115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40401152014-06-16 Spatial heterogeneity of type I error for local cluster detection tests Guttmann, Aline Li, Xinran Gaudart, Jean Gérard, Yan Demongeot, Jacques Boire, Jean-Yves Ouchchane, Lemlih Int J Health Geogr Methodology BACKGROUND: Just as power, type I error of cluster detection tests (CDTs) should be spatially assessed. Indeed, CDTs’ type I error and power have both a spatial component as CDTs both detect and locate clusters. In the case of type I error, the spatial distribution of wrongly detected clusters (WDCs) can be particularly affected by edge effect. This simulation study aims to describe the spatial distribution of WDCs and to confirm and quantify the presence of edge effect. METHODS: A simulation of 40 000 datasets has been performed under the null hypothesis of risk homogeneity. The simulation design used realistic parameters from survey data on birth defects, and in particular, two baseline risks. The simulated datasets were analyzed using the Kulldorff’s spatial scan as a commonly used test whose behavior is otherwise well known. To describe the spatial distribution of type I error, we defined the participation rate for each spatial unit of the region. We used this indicator in a new statistical test proposed to confirm, as well as quantify, the edge effect. RESULTS: The predefined type I error of 5% was respected for both baseline risks. Results showed strong edge effect in participation rates, with a descending gradient from center to edge, and WDCs more often centrally situated. CONCLUSIONS: In routine analysis of real data, clusters on the edge of the region should be carefully considered as they rarely occur when there is no cluster. Further work is needed to combine results from power studies with this work in order to optimize CDTs performance. BioMed Central 2014-05-27 /pmc/articles/PMC4040115/ /pubmed/24885343 http://dx.doi.org/10.1186/1476-072X-13-15 Text en Copyright © 2014 Guttmann et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Guttmann, Aline Li, Xinran Gaudart, Jean Gérard, Yan Demongeot, Jacques Boire, Jean-Yves Ouchchane, Lemlih Spatial heterogeneity of type I error for local cluster detection tests |
title | Spatial heterogeneity of type I error for local cluster detection tests |
title_full | Spatial heterogeneity of type I error for local cluster detection tests |
title_fullStr | Spatial heterogeneity of type I error for local cluster detection tests |
title_full_unstemmed | Spatial heterogeneity of type I error for local cluster detection tests |
title_short | Spatial heterogeneity of type I error for local cluster detection tests |
title_sort | spatial heterogeneity of type i error for local cluster detection tests |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4040115/ https://www.ncbi.nlm.nih.gov/pubmed/24885343 http://dx.doi.org/10.1186/1476-072X-13-15 |
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