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Fine-mapping using the weighted average method for a case-control study
We present a new method for fine-mapping a disease susceptibility locus using a case-control design. The new method, termed the weighted average (WA) statistic, averages the Cochran-Armitage (CA) trend test statistic and the difference between the Hardy-Weinberg disequilibrium test statistic for cas...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866715/ https://www.ncbi.nlm.nih.gov/pubmed/16451680 http://dx.doi.org/10.1186/1471-2156-6-S1-S67 |
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author | Song, Kijoung Orloff, Mohammed S Lu, Qing Elston, Robert C |
author_facet | Song, Kijoung Orloff, Mohammed S Lu, Qing Elston, Robert C |
author_sort | Song, Kijoung |
collection | PubMed |
description | We present a new method for fine-mapping a disease susceptibility locus using a case-control design. The new method, termed the weighted average (WA) statistic, averages the Cochran-Armitage (CA) trend test statistic and the difference between the Hardy-Weinberg disequilibrium test statistic for cases and controls (the HWD trend). The main characteristics of the WA statistic are that it improves on the weaknesses, and maintains the strengths, of both the CA trend test and the HWD trend test. Data from three different populations in the Genetic Analysis Workshop 14 (GAW14) simulated dataset (Aipotu, Karangar, and Danacaa) were first subjected to model-free linkage analysis to find regions exhibiting linkage. Then, for fine-scale mapping, 140 SNPs within the significant linkage regions were analyzed with the WA test statistic on replicates of the three populations, both separately and combined. The regions that were significant in the multipoint linkage analysis were also significant in this fine-scale mapping. The most significant regions that were obtained using the WA statistic were regions in chromosome 3 (B03T3056–B03T3058, p-value < 1 × 10(-10 )) and chromosome 9 (B09T8332–B09T8334, p-value 1 × 10(-6 )). Based on the results of the simulated GAW14 data, the WA test statistic showed good performance and could narrow down the region containing the susceptibility locus. However, the strength of the signal depends on both the strength of the linkage disequilibrium and the heterozygosity of the linked marker. |
format | Text |
id | pubmed-1866715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18667152007-05-11 Fine-mapping using the weighted average method for a case-control study Song, Kijoung Orloff, Mohammed S Lu, Qing Elston, Robert C BMC Genet Proceedings We present a new method for fine-mapping a disease susceptibility locus using a case-control design. The new method, termed the weighted average (WA) statistic, averages the Cochran-Armitage (CA) trend test statistic and the difference between the Hardy-Weinberg disequilibrium test statistic for cases and controls (the HWD trend). The main characteristics of the WA statistic are that it improves on the weaknesses, and maintains the strengths, of both the CA trend test and the HWD trend test. Data from three different populations in the Genetic Analysis Workshop 14 (GAW14) simulated dataset (Aipotu, Karangar, and Danacaa) were first subjected to model-free linkage analysis to find regions exhibiting linkage. Then, for fine-scale mapping, 140 SNPs within the significant linkage regions were analyzed with the WA test statistic on replicates of the three populations, both separately and combined. The regions that were significant in the multipoint linkage analysis were also significant in this fine-scale mapping. The most significant regions that were obtained using the WA statistic were regions in chromosome 3 (B03T3056–B03T3058, p-value < 1 × 10(-10 )) and chromosome 9 (B09T8332–B09T8334, p-value 1 × 10(-6 )). Based on the results of the simulated GAW14 data, the WA test statistic showed good performance and could narrow down the region containing the susceptibility locus. However, the strength of the signal depends on both the strength of the linkage disequilibrium and the heterozygosity of the linked marker. BioMed Central 2005-12-30 /pmc/articles/PMC1866715/ /pubmed/16451680 http://dx.doi.org/10.1186/1471-2156-6-S1-S67 Text en Copyright © 2005 Song et al; licensee BioMed Central Ltd http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Proceedings Song, Kijoung Orloff, Mohammed S Lu, Qing Elston, Robert C Fine-mapping using the weighted average method for a case-control study |
title | Fine-mapping using the weighted average method for a case-control study |
title_full | Fine-mapping using the weighted average method for a case-control study |
title_fullStr | Fine-mapping using the weighted average method for a case-control study |
title_full_unstemmed | Fine-mapping using the weighted average method for a case-control study |
title_short | Fine-mapping using the weighted average method for a case-control study |
title_sort | fine-mapping using the weighted average method for a case-control study |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866715/ https://www.ncbi.nlm.nih.gov/pubmed/16451680 http://dx.doi.org/10.1186/1471-2156-6-S1-S67 |
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