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Hypothesis testing of meiotic recombination rates from population genetic data

BACKGROUND: Meiotic recombination, one of the central biological processes studied in population genetics, comes in two known forms: crossovers and gene conversions. A number of previous studies have shown that when one of these two events is nonexistent in the genealogical model, the point estimati...

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Autor principal: Yin, Junming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267743/
https://www.ncbi.nlm.nih.gov/pubmed/25433522
http://dx.doi.org/10.1186/s12863-014-0122-7
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author Yin, Junming
author_facet Yin, Junming
author_sort Yin, Junming
collection PubMed
description BACKGROUND: Meiotic recombination, one of the central biological processes studied in population genetics, comes in two known forms: crossovers and gene conversions. A number of previous studies have shown that when one of these two events is nonexistent in the genealogical model, the point estimation of the corresponding recombination rate by population genetic methods tends to be inflated. Therefore, it has become necessary to obtain statistical evidence from population genetic data about whether one of the two recombination events is absent. RESULTS: In this paper, we formulate this problem in a hypothesis testing framework and devise a testing procedure based on the likelihood ratio test (LRT). However, because the null value (i.e., zero) lies on the boundary of the parameter space, the regularity conditions for the large‐sample approximation to the distribution of the LRT statistic do not apply. In turn, the standard chi‐squared approximation is inaccurate. To address this critical issue, we propose a parametric bootstrap procedure to obtain an approximate p‐value for the observed test statistic. Coalescent simulations are conducted to show that our approach yields accurate null p‐values that closely follow the theoretical prediction while the estimated alternative p‐values tend to concentrate closer to zero. Finally, the method is demonstrated on a real biological data set from the telomere of the X chromosome of African Drosophila melanogaster. CONCLUSIONS: Our methodology provides a necessary complement to the existing procedures of estimating meiotic recombination rates from population genetic data. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12863-014-0122-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-42677432014-12-17 Hypothesis testing of meiotic recombination rates from population genetic data Yin, Junming BMC Genet Methodology Article BACKGROUND: Meiotic recombination, one of the central biological processes studied in population genetics, comes in two known forms: crossovers and gene conversions. A number of previous studies have shown that when one of these two events is nonexistent in the genealogical model, the point estimation of the corresponding recombination rate by population genetic methods tends to be inflated. Therefore, it has become necessary to obtain statistical evidence from population genetic data about whether one of the two recombination events is absent. RESULTS: In this paper, we formulate this problem in a hypothesis testing framework and devise a testing procedure based on the likelihood ratio test (LRT). However, because the null value (i.e., zero) lies on the boundary of the parameter space, the regularity conditions for the large‐sample approximation to the distribution of the LRT statistic do not apply. In turn, the standard chi‐squared approximation is inaccurate. To address this critical issue, we propose a parametric bootstrap procedure to obtain an approximate p‐value for the observed test statistic. Coalescent simulations are conducted to show that our approach yields accurate null p‐values that closely follow the theoretical prediction while the estimated alternative p‐values tend to concentrate closer to zero. Finally, the method is demonstrated on a real biological data set from the telomere of the X chromosome of African Drosophila melanogaster. CONCLUSIONS: Our methodology provides a necessary complement to the existing procedures of estimating meiotic recombination rates from population genetic data. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12863-014-0122-7) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-30 /pmc/articles/PMC4267743/ /pubmed/25433522 http://dx.doi.org/10.1186/s12863-014-0122-7 Text en © Yin; licensee BioMed Central Ltd. 2014 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.
spellingShingle Methodology Article
Yin, Junming
Hypothesis testing of meiotic recombination rates from population genetic data
title Hypothesis testing of meiotic recombination rates from population genetic data
title_full Hypothesis testing of meiotic recombination rates from population genetic data
title_fullStr Hypothesis testing of meiotic recombination rates from population genetic data
title_full_unstemmed Hypothesis testing of meiotic recombination rates from population genetic data
title_short Hypothesis testing of meiotic recombination rates from population genetic data
title_sort hypothesis testing of meiotic recombination rates from population genetic data
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267743/
https://www.ncbi.nlm.nih.gov/pubmed/25433522
http://dx.doi.org/10.1186/s12863-014-0122-7
work_keys_str_mv AT yinjunming hypothesistestingofmeioticrecombinationratesfrompopulationgeneticdata