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Recent Demographic History Inferred by High-Resolution Analysis of Linkage Disequilibrium.
Santiago, Enrique; Novo, Irene; Pardiñas, Antonio F; Saura, María; Wang, Jinliang; Caballero, Armando.
Afiliação
  • Santiago E; Departamento de Biología Funcional, Facultad de Biología, Universidad de Oviedo, Oviedo, Spain.
  • Novo I; Centro de Investigación Mariña, Departamento de Bioquímica, Genética e Inmunología, Edificio CC Experimentais, Campus de Vigo, Universidade de Vigo, Vigo, Spain.
  • Pardiñas AF; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, United Kingdom.
  • Saura M; Departamento de Mejora Genética Animal, INIA, Madrid, Spain.
  • Wang J; Institute of Zoology, Zoological Society of London, London, United Kingdom.
  • Caballero A; Centro de Investigación Mariña, Departamento de Bioquímica, Genética e Inmunología, Edificio CC Experimentais, Campus de Vigo, Universidade de Vigo, Vigo, Spain.
Mol Biol Evol ; 37(12): 3642-3653, 2020 12 16.
Article em En | MEDLINE | ID: mdl-32642779
Inferring changes in effective population size (Ne) in the recent past is of special interest for conservation of endangered species and for human history research. Current methods for estimating the very recent historical Ne are unable to detect complex demographic trajectories involving multiple episodes of bottlenecks, drops, and expansions. We develop a theoretical and computational framework to infer the demographic history of a population within the past 100 generations from the observed spectrum of linkage disequilibrium (LD) of pairs of loci over a wide range of recombination rates in a sample of contemporary individuals. The cumulative contributions of all of the previous generations to the observed LD are included in our model, and a genetic algorithm is used to search for the sequence of historical Ne values that best explains the observed LD spectrum. The method can be applied from large samples to samples of fewer than ten individuals using a variety of genotyping and DNA sequencing data: haploid, diploid with phased or unphased genotypes and pseudohaploid data from low-coverage sequencing. The method was tested by computer simulation for sensitivity to genotyping errors, temporal heterogeneity of samples, population admixture, and structural division into subpopulations, showing high tolerance to deviations from the assumptions of the model. Computer simulations also show that the proposed method outperforms other leading approaches when the inference concerns recent timeframes. Analysis of data from a variety of human and animal populations gave results in agreement with previous estimations by other methods or with records of historical events.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Recombinação Genética / Desequilíbrio de Ligação / Técnicas Genéticas / Densidade Demográfica / Modelos Genéticos Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Mol Biol Evol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Recombinação Genética / Desequilíbrio de Ligação / Técnicas Genéticas / Densidade Demográfica / Modelos Genéticos Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Mol Biol Evol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Espanha