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Fregene: Simulation of realistic sequence-level data in populations and ascertained samples
BACKGROUND: FREGENE simulates sequence-level data over large genomic regions in large populations. Because, unlike coalescent simulators, it works forwards through time, it allows complex scenarios of selection, demography, and recombination to be modelled simultaneously. Detailed tracking of sites...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2542380/ https://www.ncbi.nlm.nih.gov/pubmed/18778480 http://dx.doi.org/10.1186/1471-2105-9-364 |
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author | Chadeau-Hyam, Marc Hoggart, Clive J O'Reilly, Paul F Whittaker, John C De Iorio, Maria Balding, David J |
author_facet | Chadeau-Hyam, Marc Hoggart, Clive J O'Reilly, Paul F Whittaker, John C De Iorio, Maria Balding, David J |
author_sort | Chadeau-Hyam, Marc |
collection | PubMed |
description | BACKGROUND: FREGENE simulates sequence-level data over large genomic regions in large populations. Because, unlike coalescent simulators, it works forwards through time, it allows complex scenarios of selection, demography, and recombination to be modelled simultaneously. Detailed tracking of sites under selection is implemented in FREGENE and provides the opportunity to test theoretical predictions and gain new insights into mechanisms of selection. We describe here main functionalities of both FREGENE and SAMPLE, a companion program that can replicate association study datasets. RESULTS: We report detailed analyses of six large simulated datasets that we have made publicly available. Three demographic scenarios are modelled: one panmictic, one substructured with migration, and one complex scenario that mimics the principle features of genetic variation in major worldwide human populations. For each scenario there is one neutral simulation, and one with a complex pattern of selection. CONCLUSION: FREGENE and the simulated datasets will be valuable for assessing the validity of models for selection, demography and population genetic parameters, as well as the efficacy of association studies. Its principle advantages are modelling flexibility and computational efficiency. It is open source and object-oriented. As such, it can be customised and the range of models extended. |
format | Text |
id | pubmed-2542380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-25423802008-09-18 Fregene: Simulation of realistic sequence-level data in populations and ascertained samples Chadeau-Hyam, Marc Hoggart, Clive J O'Reilly, Paul F Whittaker, John C De Iorio, Maria Balding, David J BMC Bioinformatics Software BACKGROUND: FREGENE simulates sequence-level data over large genomic regions in large populations. Because, unlike coalescent simulators, it works forwards through time, it allows complex scenarios of selection, demography, and recombination to be modelled simultaneously. Detailed tracking of sites under selection is implemented in FREGENE and provides the opportunity to test theoretical predictions and gain new insights into mechanisms of selection. We describe here main functionalities of both FREGENE and SAMPLE, a companion program that can replicate association study datasets. RESULTS: We report detailed analyses of six large simulated datasets that we have made publicly available. Three demographic scenarios are modelled: one panmictic, one substructured with migration, and one complex scenario that mimics the principle features of genetic variation in major worldwide human populations. For each scenario there is one neutral simulation, and one with a complex pattern of selection. CONCLUSION: FREGENE and the simulated datasets will be valuable for assessing the validity of models for selection, demography and population genetic parameters, as well as the efficacy of association studies. Its principle advantages are modelling flexibility and computational efficiency. It is open source and object-oriented. As such, it can be customised and the range of models extended. BioMed Central 2008-09-08 /pmc/articles/PMC2542380/ /pubmed/18778480 http://dx.doi.org/10.1186/1471-2105-9-364 Text en Copyright © 2008 Chadeau-Hyam 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 | Software Chadeau-Hyam, Marc Hoggart, Clive J O'Reilly, Paul F Whittaker, John C De Iorio, Maria Balding, David J Fregene: Simulation of realistic sequence-level data in populations and ascertained samples |
title | Fregene: Simulation of realistic sequence-level data in populations and ascertained samples |
title_full | Fregene: Simulation of realistic sequence-level data in populations and ascertained samples |
title_fullStr | Fregene: Simulation of realistic sequence-level data in populations and ascertained samples |
title_full_unstemmed | Fregene: Simulation of realistic sequence-level data in populations and ascertained samples |
title_short | Fregene: Simulation of realistic sequence-level data in populations and ascertained samples |
title_sort | fregene: simulation of realistic sequence-level data in populations and ascertained samples |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2542380/ https://www.ncbi.nlm.nih.gov/pubmed/18778480 http://dx.doi.org/10.1186/1471-2105-9-364 |
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