The following pages link to (Q3958314):
Displaying 50 items.
- Asymptotics of the minimal clade size and related functionals of certain beta-coalescents (Q267126) (← links)
- On Hille-type approximation of degenerate semigroups of operators (Q331150) (← links)
- The conditional ancestral selection graph with strong balancing selection (Q615624) (← links)
- Coalescent theory for age-structured random mating populations with two sexes (Q648029) (← links)
- Editorial: Coalescent theory has many new branches (Q743257) (← links)
- Line-of-descent and genealogical processes, and their applications in population genetics models (Q761376) (← links)
- Lines of descent and the coalescent (Q795765) (← links)
- Wright-Fisher revisited: the case of fertility correlation (Q849563) (← links)
- On sampling distributions for coalescent processes with simultaneous multiple collisions (Q850725) (← links)
- Coalescent theory for a completely random mating monoecious population (Q876069) (← links)
- How to compute the effective size of spatiotemporally structured populations using separation of time scales (Q885384) (← links)
- New analytic results for speciation times in neutral models (Q942914) (← links)
- Lineages-through-time plots of neutral models for speciation (Q1000198) (← links)
- Allele frequencies after a bottleneck (Q1058480) (← links)
- The genetic divergence of two populations (Q1062637) (← links)
- Dual processes and an invariance result for exchangeable models in population genetics (Q1079141) (← links)
- Partition structures, Polya urns, the Ewens sampling formula, and the ages of alleles (Q1086510) (← links)
- The sampling theory of neutral alleles and an urn model in population genetics (Q1098799) (← links)
- The population genealogy of the infinitely-many neutral alleles model (Q1098800) (← links)
- Conditional genealogies and the age of a neutral mutant (Q1580702) (← links)
- A representation of exchangeable hierarchies by sampling from random real trees (Q1626599) (← links)
- On incomplete sampling under birth-death models and connections to the sampling-based coalescent (Q1628807) (← links)
- Estimation of parameters in large offspring number models and ratios of coalescence times (Q1631128) (← links)
- Strong migration limit for games in structured populations: applications to dominance hierarchy and set structure (Q1651807) (← links)
- Genealogical properties of subsamples in highly fecund populations (Q1668968) (← links)
- Multi-locus data distinguishes between population growth and multiple merger coalescents (Q1672822) (← links)
- Bayesian inference of selection in the Wright-Fisher diffusion model (Q1672824) (← links)
- Sampling-through-time in birth-death trees (Q1733035) (← links)
- Identifiability and reconstructibility of species phylogenies under a modified coalescent (Q1736939) (← links)
- Forward and backward diffusion approximations for haploid exchangeable population models. (Q1765998) (← links)
- The coalescent in population models with time-inhomogeneous environment. (Q1766045) (← links)
- Central limit theorem for the size of the range of a renewal process (Q1779682) (← links)
- Strategy abundance in evolutionary many-player games with multiple strategies (Q1783680) (← links)
- On the quantity and quality of single nucleotide polymorphisms in the human genome. (Q1888745) (← links)
- Monte Carlo inference methods in population genetics (Q1921110) (← links)
- Population genetics of neutral mutations in exponentially growing cancer cell populations (Q1948687) (← links)
- Inference of gene flow in the process of speciation: efficient maximum-likelihood implementation of a generalised isolation-with-migration model (Q2056389) (← links)
- Asymptotic genealogies for a class of generalized Wright-Fisher models (Q2122920) (← links)
- Markov genealogy processes (Q2131426) (← links)
- Developments in coalescent theory from single loci to chromosomes (Q2185189) (← links)
- An analytical framework in the general coalescent tree setting for analyzing polymorphisms created by two mutations (Q2257055) (← links)
- The distribution of the coalescence time and the number of pairwise nucleotide differences in a model of population divergence or speciation with an initial period of gene flow (Q2261878) (← links)
- Multiple merger gene genealogies in two species: monophyly, paraphyly, and polyphyly for two examples of lambda coalescents (Q2261880) (← links)
- Robust model selection between population growth and multiple merger coalescents (Q2328381) (← links)
- The site-frequency spectrum associated with \(\varXi\)-coalescents (Q2358518) (← links)
- The probability of fixation of a single mutant in an exchangeable selection model (Q2373246) (← links)
- Consistency of estimators of the population-scaled recombination rate (Q2433058) (← links)
- On the length distribution of external branches in coalescence trees: Genetic diversity within species (Q2459063) (← links)
- Excheangable partitions derived from Markovian coalescents (Q2467600) (← links)
- Genealogical theory for random mating populations with two sexes (Q2506744) (← links)
