The following pages link to (Q3156772):
Displaying 50 items.
- Importance sampling for Lambda-coalescents in the infinitely many sites model (Q299323) (← links)
- Partitioning, duality, and linkage disequilibria in the Moran model with recombination (Q304213) (← links)
- Reversible polymorphism-aware phylogenetic models and their application to tree inference (Q309245) (← links)
- The ancestry of genetic segments (Q355904) (← links)
- Probability and manipulation: evolution and simulation in applied population genetics (Q506909) (← links)
- Reuse, recycle, reweigh: combating influenza through efficient sequential Bayesian computation for massive data (Q542932) (← links)
- Asymptotic behavior of a Moran model with mutations, drift and recombination among multiple loci (Q604532) (← links)
- On the inadmissibility of Watterson's estimator (Q615423) (← links)
- Recombination, gene conversion, and identity-by-descent at three loci (Q615429) (← links)
- Estimating primate divergence times by using conditioned birth-and-death processes (Q615611) (← links)
- Considerate approaches to constructing summary statistics for ABC model selection (Q693357) (← 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)
- Path lengths in tree-child time consistent hybridization networks (Q845330) (← links)
- Consistency of estimators of population scaled parameters using composite likelihood (Q883786) (← links)
- Mutation, selection, and ancestry in branching models: a variational approach (Q883808) (← links)
- How to compute the effective size of spatiotemporally structured populations using separation of time scales (Q885384) (← links)
- An analytical upper bound on the minimum number of recombinations in the history of SNP sequences in populations (Q987779) (← links)
- The mutation process in colored coalescent theory (Q1048265) (← links)
- The effective size of bryophyte populations (Q1621100) (← links)
- Inbreeding, pedigree size, and the most recent common ancestor of humanity (Q1628851) (← links)
- Multi-locus data distinguishes between population growth and multiple merger coalescents (Q1672822) (← links)
- Population structure and coalescence in pedigrees: comparisons to the structured coalescent and a framework for inference (Q1700548) (← links)
- Inference in population genetics using forward and backward, discrete and continuous time processes (Q1752523) (← links)
- Computing the probability of gene trees concordant with the species tree in the multispecies coalescent (Q2054865) (← links)
- The distribution of waiting distances in ancestral recombination graphs (Q2056406) (← links)
- Limiting distribution of X-chromosomal coalescence times under first-cousin consanguineous mating (Q2083917) (← links)
- Combinatorial solutions to coagulation kernel for linear chains (Q2116305) (← links)
- A compendium of covariances and correlation coefficients of coalescent tree properties (Q2131418) (← links)
- Registering the evolutionary history in individual-based models of speciation (Q2153431) (← links)
- Developments in coalescent theory from single loci to chromosomes (Q2185189) (← links)
- Exact combinatorial approach to finite coagulating systems through recursive equations (Q2194261) (← links)
- Prediction of group patterns in social mammals based on a coalescent model (Q2216300) (← links)
- Coalescense with arbitrary-parameter kernels and monodisperse initial conditions: a study within combinatorial framework (Q2236906) (← links)
- Probabilistic analysis of a genealogical model of animal group patterns (Q2340018) (← links)
- A new general analytical approach for modeling patterns of genetic differentiation and effective size of subdivided populations over time (Q2343732) (← links)
- Inferring the demographic history from DNA sequences: an importance sampling approach based on non-homogeneous processes (Q2362544) (← links)
- Within a sample from a population, the distribution of the number of descendants of a subsample's most recent common ancestor (Q2444781) (← links)
- Single-crossover recombination and ancestral recombination trees (Q2447556) (← links)
- Gaussian approximations for phylogenetic branch length statistics under stochastic models of biodiversity (Q2455550) (← links)
- Beta-coalescents and continuous stable random trees (Q2456031) (← links)
- On the length distribution of external branches in coalescence trees: Genetic diversity within species (Q2459063) (← links)
- Probability that a sequence is lost without trace under the neutral Wright-Fisher model with recombination (Q2513647) (← links)
- The discrete Laplace exponential family and estimation of Y-STR haplotype frequencies (Q2634994) (← links)
- A characterisation of the reconstructed birth-death process through time rescaling (Q2661460) (← links)
- On the Height and Length of the Ancestral Recombination Graph (Q3182425) (← links)
- Similarity of States in Modal Logic (Q5213661) (← links)
- Bridging trees for posterior inference on ancestral recombination graphs (Q5243648) (← links)
- Linearization of the Kingman coalescent (Q6161968) (← links)
