The following pages link to The coalescent (Q1167483):
Displayed 50 items.
- Generalized population models and the nature of genetic drift (Q462420) (← links)
- The effect of recurrent mutation on the frequency spectrum of a segregating site and the age of an allele (Q462440) (← links)
- Markov jump processes in modeling coalescent with recombination (Q464186) (← links)
- The cut-and-paste process (Q465468) (← links)
- Quasi equilibrium, variance effective size and fixation index for populations with substructure (Q471072) (← links)
- Hitting times and interlacing eigenvalues: a stochastic approach using intertwinings (Q471527) (← links)
- Descartes' rule of signs and the identifiability of population demographic models from genomic variation data (Q482900) (← links)
- Birth-death models and coalescent point processes: the shape and probability of reconstructed phylogenies (Q487319) (← links)
- On the eigenvalue effective size of structured populations (Q493080) (← links)
- Population growth combined with wide offspring distributions can increase fixation rate and reduce genetic diversity (Q517991) (← links)
- On the moments of the absorption time of Kingman's coalescent (Q518875) (← links)
- Experiments with the site frequency spectrum (Q542030) (← links)
- The branching process with logistic growth (Q558688) (← links)
- The birth process with immigration, and the genealogical structure of large populations (Q580227) (← links)
- Cycles, permutations and the stucture of the Yule process with immigration (Q580228) (← links)
- An application of the central limit theorem to coalescence times in the structured coalescent model with strong migration (Q604546) (← links)
- Asymptotic results for coalescent processes without proper frequencies and applications to the two-parameter Poisson-Dirichlet coalescent (Q607271) (← links)
- A duality approach to the genealogies of discrete nonneutral Wright-Fisher models (Q609682) (← links)
- Gene surfing in expanding populations (Q615416) (← links)
- The distribution of the coalescence time and the number of pairwise nucleotide differences in the ``isolation with migration'' model (Q615431) (← links)
- Summary statistics of neutral mutations in longitudinal DNA samples (Q615500) (← links)
- A coalescent process with simultaneous multiple mergers for approximating the gene genealogies of many marine organisms (Q615510) (← links)
- To what extent does genealogical ancestry imply genetic ancestry? (Q615526) (← links)
- Detecting hybrid speciation in the presence of incomplete lineage sorting using gene tree incongruence: a model (Q615571) (← links)
- Duality, ancestral and diffusion processes in models with selection (Q615593) (← links)
- The genealogy, site frequency spectrum and ages of two nested mutant alleles (Q615607) (← links)
- Fixation probability with multiple alleles and projected average allelic effect on selection (Q615609) (← links)
- A coalescent dual process in a Moran model with genic selection (Q615620) (← links)
- The conditional ancestral selection graph with strong balancing selection (Q615624) (← links)
- Structured coalescent processes from a modified Moran model with large offspring numbers (Q615647) (← links)
- Limit theorems for sequences of random trees (Q619105) (← links)
- The tree length of an evolving coalescent (Q662824) (← links)
- The distribution of \(F_{st}\) and other genetic statistics for a class of population structure models (Q663124) (← links)
- On the block counting process and the fixation line of the Bolthausen-Sznitman coalescent (Q681993) (← links)
- The coalescent in two colonies with symmetric migration (Q688488) (← links)
- Smaller population size at the MRCA time for stationary branching processes (Q690871) (← links)
- The asymptotic distribution of the length of beta-coalescent trees (Q691115) (← links)
- Effective game matrix and inclusive payoff in group-structured populations (Q692091) (← links)
- On the robustness of the extension of the one-third law of evolution to the multi-player game (Q692099) (← links)
- A non-zero variance of Tajima's estimator for two sequences even for infinitely many unlinked loci (Q725142) (← links)
- On the joint distribution of tree height and tree length under the coalescent (Q725147) (← links)
- An efficient algorithm for generating the internal branches of a Kingman coalescent (Q725150) (← links)
- Wright-Fisher diffusion bridges (Q725151) (← links)
- Hypothesis tests for phylogenetic quartets, with applications to coalescent-based species tree inference (Q727146) (← links)
- Small-time behavior of beta coalescents (Q731663) (← links)
- Nonlinear effects in evolution - an \textit{ab initio} study: a model in which the classical theory of evolution occurs as a special case (Q738663) (← links)
- Revisiting the time until fixation of a neutral mutant in a finite population -- a coalescent theory approach (Q739192) (← links)
- The effect of inbreeding constraints and offspring distribution on time to the most recent common ancestor (Q739321) (← links)
- Editorial: Coalescent theory has many new branches (Q743257) (← links)
- On the extended Moran model and its relation to coalescents with multiple collisions (Q743258) (← links)