ArticleGenetics2013
An ancestral recombination graph for diploid populations with skewed offspring distribution.
Article in Genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.
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Who cites it
21 citing papers in PubMed.
- PhaseGen: exact solutions for time-inhomogeneous multivariate coalescent distributions under diverse demographies.Genetics · 2026Article
- Genomic perspectives on the inference of evolutionary changes in ecological life-history traits.Quantitative plant biology · 2026Review
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- A general and efficient representation of ancestral recombination graphs.bioRxiv : the preprint server for biology · 2024Article
- Inference of Coalescence Times and Variant Ages Using Convolutional Neural Networks.Molecular biology and evolution · 2023Article
- Interpreting the pervasive observation of U-shaped Site Frequency Spectra.PLoS genetics · 2023Article
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- Pedigree in the biparental Moran model.Journal of mathematical biology · 2022Article
- Efficient ancestry and mutation simulation with msprime 1.0.Genetics · 2022Article
- Sweepstake reproductive success and collective dispersal produce chaotic genetic patchiness in a broadcast spawner.Science advances · 2021Article
- Separation of timescales for the seed bank diffusion and its jump-diffusion limit.Journal of mathematical biology · 2021Article
- Considering Genomic Scans for Selection as Coalescent Model Choice.Genome biology and evolution · 2020Article
- Coalescent Processes with Skewed Offspring Distributions and Nonequilibrium Demography.Genetics · 2018Article
- Current hypotheses to explain genetic chaos under the sea.Current zoology · 2016Article
- On the importance of skewed offspring distributions and background selection in virus population genetics.Heredity · 2016Review
- The Site Frequency Spectrum for General Coalescents.Genetics · 2016Article
- Can the site-frequency spectrum distinguish exponential population growth from multiple-merger coalescents?Genetics · 2015Article
- Article
- Statistical properties of the site-frequency spectrum associated with lambda-coalescents.Genetics · 2013Article
- The importance and application of the ancestral recombination graph.Frontiers in genetics · 2013Article
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3 authors.
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Abstract
A large offspring-number diploid biparental multilocus population model of Moran type is our object of study. At each time step, a pair of diploid individuals drawn uniformly at random contributes offspring to the population. The number of offspring can be large relative to the total population size. Similar "heavily skewed" reproduction mechanisms have been recently considered by various authors (cf. e.g., Eldon and Wakeley 2006, 2008) and reviewed by Hedgecock and Pudovkin (2011). Each diploid parental individual contributes exactly one chromosome to each diploid offspring, and hence ancestral lineages can coalesce only when in distinct individuals. A separation-of-timescales phenomenon is thus observed. A result of Möhle (1998) is extended to obtain convergence of the ancestral process to an ancestral recombination graph necessarily admitting simultaneous multiple mergers of ancestral lineages. The usual ancestral recombination graph is obtained as a special case of our model when the parents contribute only one offspring to the population each time. Due to diploidy and large offspring numbers, novel effects appear. For example, the marginal genealogy at each locus admits simultaneous multiple mergers in up to four groups, and different loci remain substantially correlated even as the recombination rate grows large. Thus, genealogies for loci far apart on the same chromosome remain correlated. Correlation in coalescence times for two loci is derived and shown to be a function of the coalescence parameters of our model. Extending the observations by Eldon and Wakeley (2008), predictions of linkage disequilibrium are shown to be functions of the reproduction parameters of our model, in addition to the recombination rate. Correlations in ratios of coalescence times between loci can be high, even when the recombination rate is high and sample size is large, in large offspring-number populations, as suggested by simulations, hinting at how to distinguish between different population models.
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