Pages that link to "Item:Q1212885"
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The following pages link to On the number of segregating sites in genetical models without recombination (Q1212885):
Displaying 50 items.
- Segregating sites in a gene conversion model with mutation (Q1281376) (← links)
- The time to the ancestor along sequences with recombination (Q1289342) (← links)
- The role of population size in molecular evolution (Q1289343) (← links)
- Some statistical improvements for estimating population size and mutation rate from segregating sites in DNA sequences (Q1296931) (← links)
- Recombination as a point process along sequences (Q1296932) (← links)
- Coalescing into the 21st century: An overview and prospects of coalescent theory (Q1303984) (← links)
- Ages of mutations on a coalescent tree (Q1306969) (← links)
- Scale-free networks in evolution (Q1394691) (← links)
- Some notes on the combinatorial properties of haplotype tagging (Q1410355) (← links)
- The coalescent in an island model of population subdivision with variation among demes. (Q1427684) (← links)
- The ages of mutations in gene trees (Q1578585) (← links)
- The Wright-Fisher site frequency spectrum as a perturbation of the coalescent's (Q1625434) (← links)
- Estimation of parameters in large offspring number models and ratios of coalescence times (Q1631128) (← 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)
- Variance in estimated pairwise genetic distance under high versus low coverage sequencing: the contribution of linkage disequilibrium (Q1746104) (← links)
- The third moments of the site frequency spectrum (Q1746157) (← links)
- Single and simultaneous binary mergers in Wright-Fisher genealogies (Q1750176) (← links)
- Inference in population genetics using forward and backward, discrete and continuous time processes (Q1752523) (← links)
- Central limit theorem for the size of the range of a renewal process (Q1779682) (← links)
- Self-organized criticality attributed to a central limit-like convergence effect (Q1783316) (← links)
- On parameters of the human genome (Q1786447) (← links)
- Unrooted genealogical tree probabilities in the infinitely-many-sites model (Q1804843) (← links)
- The average number of sites separating DNA sequences drawn from a subdivided population (Q1820719) (← links)
- Properties of a neutral allele model with intragenic recombination (Q1836461) (← links)
- The distribution of nucleotide site differences between two finite sequences (Q1837127) (← links)
- Monte Carlo inference methods in population genetics (Q1921110) (← links)
- Tree-valued Fleming-Viot dynamics with mutation and selection (Q1931328) (← links)
- Tree-valued resampling dynamics martingale problems and applications (Q1950379) (← links)
- Editorial: Analysis of author gender in TPB, 1991--2018 (Q1999479) (← links)
- An empirical approach to demographic inference with genomic data (Q1999490) (← links)
- Testing neutrality at copy-number-variable loci under the finite-allele and finite-site models (Q2011527) (← links)
- An approximate stationary solution for multi-allele neutral diffusion with low mutation rates (Q2011531) (← links)
- Rate matrix estimation from site frequency data (Q2014385) (← links)
- A nearly-neutral biallelic Moran model with biased mutation and linear and quadratic selection (Q2056261) (← links)
- Inference of gene flow in the process of speciation: efficient maximum-likelihood implementation of a generalised isolation-with-migration model (Q2056389) (← links)
- Exact site frequency spectra of neutrally evolving tumors: a transition between power laws reveals a signature of cell viability (Q2076094) (← links)
- Variances and covariances of linear summary statistics of segregating sites (Q2152691) (← links)
- Developments in coalescent theory from single loci to chromosomes (Q2185189) (← links)
- Sequential importance sampling for multiresolution Kingman-Tajima coalescent counting (Q2194460) (← links)
- Scale invariant correlations between genes and SNPs on human chromosome 1 reveal potential evolutionary mechanisms (Q2209946) (← links)
- An analytical framework in the general coalescent tree setting for analyzing polymorphisms created by two mutations (Q2257055) (← links)
- The joint allele frequency spectrum of multiple populations: a coalescent theory approach (Q2261866) (← links)
- The allele-frequency spectrum in a decoupled Moran model with mutation, drift, and directional selection, assuming small mutation rates (Q2261868) (← 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)
- Tree lengths for general \(\Lambda \)-coalescents and the asymptotic site frequency spectrum around the Bolthausen-Sznitman coalescent (Q2286448) (← links)
- Robust model selection between population growth and multiple merger coalescents (Q2328381) (← links)
- Finding the best resolution for the Kingman-Tajima coalescent: theory and applications (Q2339969) (← links)
- The site-frequency spectrum associated with \(\varXi\)-coalescents (Q2358518) (← links)
- The neutral frequency spectrum of linked sites (Q2413541) (← links)