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On different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis
An empirical comparison between three different methods for estimation of pair-wise identity-by-descent (IBD) sharing at marker loci was conducted in order to quantify the resulting differences in power and localization precision in variance components-based linkage analysis. On the examined simulat...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866511/ https://www.ncbi.nlm.nih.gov/pubmed/14975140 http://dx.doi.org/10.1186/1471-2156-4-S1-S72 |
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author | Göring, Harald HH Williams, Jeff T Dyer, Thomas D Blangero, John |
author_facet | Göring, Harald HH Williams, Jeff T Dyer, Thomas D Blangero, John |
author_sort | Göring, Harald HH |
collection | PubMed |
description | An empirical comparison between three different methods for estimation of pair-wise identity-by-descent (IBD) sharing at marker loci was conducted in order to quantify the resulting differences in power and localization precision in variance components-based linkage analysis. On the examined simulated, error-free data set, it was found that an increase in accuracy of allele sharing calculation resulted in an increase in power to detect linkage. Linkage analysis based on approximate multi-marker IBD matrices computed by a Markov chain Monte Carlo approach was much more powerful than linkage analysis based on exact single-marker IBD probabilities. A "multiple two-point" approximation to true "multipoint" IBD computation was found to be roughly intermediate in power. Both multi-marker approaches were similar to each other in accuracy of localization of the quantitative trait locus and far superior to the single-marker approach. The overall conclusions of this study with respect to power are expected to also hold for different data structures and situations, even though the degree of superiority of one approach over another depends on the specific circumstances. It should be kept in mind, however, that an increase in computational accuracy is expected to go hand in hand with a decrease in robustness to various sources of errors. |
format | Text |
id | pubmed-1866511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18665112007-05-11 On different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis Göring, Harald HH Williams, Jeff T Dyer, Thomas D Blangero, John BMC Genet Proceedings An empirical comparison between three different methods for estimation of pair-wise identity-by-descent (IBD) sharing at marker loci was conducted in order to quantify the resulting differences in power and localization precision in variance components-based linkage analysis. On the examined simulated, error-free data set, it was found that an increase in accuracy of allele sharing calculation resulted in an increase in power to detect linkage. Linkage analysis based on approximate multi-marker IBD matrices computed by a Markov chain Monte Carlo approach was much more powerful than linkage analysis based on exact single-marker IBD probabilities. A "multiple two-point" approximation to true "multipoint" IBD computation was found to be roughly intermediate in power. Both multi-marker approaches were similar to each other in accuracy of localization of the quantitative trait locus and far superior to the single-marker approach. The overall conclusions of this study with respect to power are expected to also hold for different data structures and situations, even though the degree of superiority of one approach over another depends on the specific circumstances. It should be kept in mind, however, that an increase in computational accuracy is expected to go hand in hand with a decrease in robustness to various sources of errors. BioMed Central 2003-12-31 /pmc/articles/PMC1866511/ /pubmed/14975140 http://dx.doi.org/10.1186/1471-2156-4-S1-S72 Text en Copyright © 2003 Göring 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 Göring, Harald HH Williams, Jeff T Dyer, Thomas D Blangero, John On different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis |
title | On different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis |
title_full | On different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis |
title_fullStr | On different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis |
title_full_unstemmed | On different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis |
title_short | On different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis |
title_sort | on different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866511/ https://www.ncbi.nlm.nih.gov/pubmed/14975140 http://dx.doi.org/10.1186/1471-2156-4-S1-S72 |
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