scientific article; zbMATH DE number 6747572
From MaRDI portal
Publication:5282824
zbMath1366.92001MaRDI QIDQ5282824
Publication date: 17 July 2017
Title: zbMATH Open Web Interface contents unavailable due to conflicting licenses.
Problems related to evolution (92D15) Protein sequences, DNA sequences (92D20) Introductory exposition (textbooks, tutorial papers, etc.) pertaining to biology (92-01)
Related Items (only showing first 100 items - show all)
Consistency and inconsistency of consensus methods for inferring species trees from gene trees in the presence of ancestral population structure ⋮ Inferring the demographic history from DNA sequences: an importance sampling approach based on non-homogeneous processes ⋮ Mutation-selection equilibrium in games with multiple strategies ⋮ Topological linkage disequilibrium calculated from coalescent genealogies ⋮ The Wright-Fisher site frequency spectrum as a perturbation of the coalescent's ⋮ A compendium of covariances and correlation coefficients of coalescent tree properties ⋮ Markov genealogy processes ⋮ An individual-based model for the Lenski experiment, and the deceleration of the relative fitness ⋮ How mutation affects evolutionary games on graphs ⋮ Prosperity is associated with instability in dynamical networks ⋮ The coalescent tree of a Markov branching process with generalised logistic growth ⋮ Spatially explicit neutral models for population genetics and community ecology: extensions of the Neyman-Scott clustering process ⋮ Modeling sequence evolution in acute HIV-1 infection ⋮ Estimation of parameters in large offspring number models and ratios of coalescence times ⋮ Epistasis can increase multivariate trait diversity in haploid non-recombining populations ⋮ Site pattern probabilities under the multispecies coalescent and a relaxed molecular clock: theory and applications ⋮ Partitioning, duality, and linkage disequilibria in the Moran model with recombination ⋮ Additive genetic variation and evolvability of a multivariate trait can be increased by epistatic gene action ⋮ Enumeration of binary trees compatible with a perfect phylogeny ⋮ Looking down in the ancestral selection graph: a probabilistic approach to the common ancestor type distribution ⋮ Social evolution and genetic interactions in the short and long term ⋮ Statistical challenges in tracking the evolution of SARS-CoV-2 ⋮ Neutral community theory: How stochasticity and dispersal-limitation can explain species coexistence ⋮ Variances and covariances of linear summary statistics of segregating sites ⋮ The process of most recent common ancestors in an evolving coalescent ⋮ The bounded coalescent model: conditioning a genealogy on a minimum root date ⋮ Tokunaga and Horton self-similarity for level set trees of Markov chains ⋮ An alternative derivation of the stationary distribution of the multivariate neutral Wright-Fisher model for low mutation rates with a view to mutation rate estimation from site frequency data ⋮ Recursions for the exchangeable partition function of the seedbank coalescent ⋮ Fixation probabilities in evolutionary dynamics under weak selection ⋮ A game-theoretical dynamic imitation model on networks ⋮ Genealogical properties of subsamples in highly fecund populations ⋮ Bayesian inference of selection in the Wright-Fisher diffusion model ⋮ Non-parametric estimation of population size changes from the site frequency spectrum ⋮ Asymptotic genealogies of interacting particle systems with an application to sequential Monte Carlo ⋮ Genealogies and ages of cultural traits: an application of the theory of duality to the research on cultural evolution ⋮ Strong seed-bank effects in bacterial evolution ⋮ Developments in coalescent theory from single loci to chromosomes ⋮ The popularity spectrum applied to a cross-cultural question ⋮ The conditional ancestral selection graph with strong balancing selection ⋮ Study the genetic variation using eta functions ⋮ Population structure and coalescence in pedigrees: comparisons to the structured coalescent and a framework for inference ⋮ Measures of success in a class of evolutionary models with fixed population size and structure ⋮ Global migration can lead to stronger spatial selection than local migration ⋮ Exact limits of inference in coalescent models ⋮ Generalized population models and the nature of genetic drift ⋮ On the size distribution of private microsatellite alleles ⋮ Single-crossover recombination and ancestral recombination trees ⋮ A survey of migration-selection models in population genetics ⋮ A mathematical formalism for natural selection with arbitrary spatial and genetic structure ⋮ Competing islands limit the rate of adaptation in structured populations ⋮ A probabilistic view on the deterministic mutation-selection equation: dynamics, equilibria, and ancestry via individual lines of descent ⋮ Identifiability of phylogenetic parameters from \(k\)-mer data under the coalescent ⋮ Identifying species network features from gene tree quartets under the coalescent model ⋮ An ancestral process with selection in an ecological community ⋮ Statistical tools for seed bank detection ⋮ Probability and manipulation: evolution and simulation in applied population genetics ⋮ Forward and backward evolutionary processes and allele frequency spectrum in a cancer cell population ⋮ Computing the joint distribution of the total tree length across loci in populations with variable size ⋮ The third moments of the site frequency spectrum ⋮ Population growth combined with wide offspring distributions can increase fixation rate and reduce genetic diversity ⋮ Inference in population genetics using forward and backward, discrete and continuous time processes ⋮ Fixation probabilities of strategies for bimatrix games in finite populations ⋮ Phase-type distributions in population genetics ⋮ An analytical framework in the general coalescent tree setting for analyzing polymorphisms created by two mutations ⋮ Time to the MRCA of a sample in a Wright-Fisher model with variable population size ⋮ The mapping of epistatic effects onto a genealogical tree in haploid populations ⋮ Multiple merger gene genealogies in two species: monophyly, paraphyly, and polyphyly for two examples of lambda coalescents ⋮ Hypothesis testing near singularities and boundaries ⋮ Strategy abundance in evolutionary many-player games with multiple strategies ⋮ Separation of timescales for the seed bank diffusion and its jump-diffusion limit ⋮ A non-zero variance of Tajima's estimator for two sequences even for infinitely many unlinked loci ⋮ On the joint distribution of tree height and tree length under the coalescent ⋮ The ubiquitous Ewens sampling formula ⋮ Conditions for neutral speciation via isolation by distance ⋮ Tree lengths for general \(\Lambda \)-coalescents and the asymptotic site frequency spectrum around the Bolthausen-Sznitman coalescent ⋮ Lineages-through-time plots of neutral models for speciation ⋮ Probability that a sequence is lost without trace under the neutral Wright-Fisher model with recombination ⋮ Neutral competition in a deterministically changing environment: revisiting continuum approaches ⋮ The largest strongly connected component in the cyclical pedigree model of Wakeley et al. ⋮ Genealogical distances under low levels of selection ⋮ Local fluctuations of genetic processes defined on two time scales, with applications to effective size estimation ⋮ The effect of inbreeding constraints and offspring distribution on time to the most recent common ancestor ⋮ Bayesian-weighted triplet and quartet methods for species tree inference ⋮ Editorial: Coalescent theory has many new branches ⋮ On spatial coalescents with multiple mergers in two dimensions ⋮ Inference in two dimensions: allele frequencies versus lengths of shared sequence blocks ⋮ Coevolution fails to maintain genetic variation in a host-parasite model with constant finite population size ⋮ Time to extinction of a cultural trait in an overlapping generation model ⋮ Variance and limiting distribution of coalescence times in a diploid model of a consanguineous population ⋮ Multivariate phase-type theory for the site frequency spectrum ⋮ Dynamics of a birth-death process based on combinatorial innovation ⋮ Evolution in range expansions with competition at rough boundaries ⋮ Coalescent models derived from birth-death processes ⋮ Limiting distribution of X-chromosomal coalescence times under first-cousin consanguineous mating ⋮ The evolving Moran genealogy ⋮ The internal branch lengths of the Kingman coalescent ⋮ Evolutionary multiplayer games ⋮ Estimating the relative rate of recombination to mutation in bacteria from single-locus variants using composite likelihood methods ⋮ The existence and abundance of ghost ancestors in biparental populations
This page was built for publication:
