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Forward-Time Simulations of Human Populations with Complex Diseases
Due to the increasing power of personal computers, as well as the availability of flexible forward-time simulation programs like simuPOP, it is now possible to simulate the evolution of complex human diseases using a forward-time approach. This approach is potentially more powerful than the coalesce...
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1829403/ https://www.ncbi.nlm.nih.gov/pubmed/17381243 http://dx.doi.org/10.1371/journal.pgen.0030047 |
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author | Peng, Bo Amos, Christopher I Kimmel, Marek |
author_facet | Peng, Bo Amos, Christopher I Kimmel, Marek |
author_sort | Peng, Bo |
collection | PubMed |
description | Due to the increasing power of personal computers, as well as the availability of flexible forward-time simulation programs like simuPOP, it is now possible to simulate the evolution of complex human diseases using a forward-time approach. This approach is potentially more powerful than the coalescent approach since it allows simulations of more than one disease susceptibility locus using almost arbitrary genetic and demographic models. However, the application of such simulations has been deterred by the lack of a suitable simulation framework. For example, it is not clear when and how to introduce disease mutants—especially those under purifying selection—to an evolving population, and how to control the disease allele frequencies at the last generation. In this paper, we introduce a forward-time simulation framework that allows us to generate large multi-generation populations with complex diseases caused by unlinked disease susceptibility loci, according to specified demographic and evolutionary properties. Unrelated individuals, small or large pedigrees can be drawn from the resulting population and provide samples for a wide range of study designs and ascertainment methods. We demonstrate our simulation framework using three examples that map genes associated with affection status, a quantitative trait, and the age of onset of a hypothetical cancer, respectively. Nonadditive fitness models, population structure, and gene–gene interactions are simulated. Case-control, sibpair, and large pedigree samples are drawn from the simulated populations and are examined by a variety of gene-mapping methods. |
format | Text |
id | pubmed-1829403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-18294032007-03-30 Forward-Time Simulations of Human Populations with Complex Diseases Peng, Bo Amos, Christopher I Kimmel, Marek PLoS Genet Research Article Due to the increasing power of personal computers, as well as the availability of flexible forward-time simulation programs like simuPOP, it is now possible to simulate the evolution of complex human diseases using a forward-time approach. This approach is potentially more powerful than the coalescent approach since it allows simulations of more than one disease susceptibility locus using almost arbitrary genetic and demographic models. However, the application of such simulations has been deterred by the lack of a suitable simulation framework. For example, it is not clear when and how to introduce disease mutants—especially those under purifying selection—to an evolving population, and how to control the disease allele frequencies at the last generation. In this paper, we introduce a forward-time simulation framework that allows us to generate large multi-generation populations with complex diseases caused by unlinked disease susceptibility loci, according to specified demographic and evolutionary properties. Unrelated individuals, small or large pedigrees can be drawn from the resulting population and provide samples for a wide range of study designs and ascertainment methods. We demonstrate our simulation framework using three examples that map genes associated with affection status, a quantitative trait, and the age of onset of a hypothetical cancer, respectively. Nonadditive fitness models, population structure, and gene–gene interactions are simulated. Case-control, sibpair, and large pedigree samples are drawn from the simulated populations and are examined by a variety of gene-mapping methods. Public Library of Science 2007-03 2007-03-23 /pmc/articles/PMC1829403/ /pubmed/17381243 http://dx.doi.org/10.1371/journal.pgen.0030047 Text en Copyright: © 2007 Peng et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Peng, Bo Amos, Christopher I Kimmel, Marek Forward-Time Simulations of Human Populations with Complex Diseases |
title | Forward-Time Simulations of Human Populations with Complex Diseases |
title_full | Forward-Time Simulations of Human Populations with Complex Diseases |
title_fullStr | Forward-Time Simulations of Human Populations with Complex Diseases |
title_full_unstemmed | Forward-Time Simulations of Human Populations with Complex Diseases |
title_short | Forward-Time Simulations of Human Populations with Complex Diseases |
title_sort | forward-time simulations of human populations with complex diseases |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1829403/ https://www.ncbi.nlm.nih.gov/pubmed/17381243 http://dx.doi.org/10.1371/journal.pgen.0030047 |
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