Pages that link to "Item:Q1212885"

The following pages link to On the number of segregating sites in genetical models without recombination (Q1212885):

Displaying 50 items.

• Reconstructing transmission trees for communicable diseases using densely sampled genetic data (Q288603) (← links)
• Importance sampling for Lambda-coalescents in the infinitely many sites model (Q299323) (← links)
• Epistasis can increase multivariate trait diversity in haploid non-recombining populations (Q299357) (← links)
• Inference of directional selection and mutation parameters assuming equilibrium (Q304438) (← links)
• Reversible polymorphism-aware phylogenetic models and their application to tree inference (Q309245) (← 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)
• Experiments with the site frequency spectrum (Q542030) (← links)
• The molecular nature of allelic diversity for two models of balancing selection (Q583148) (← links)
• On the inadmissibility of Watterson's estimator (Q615423) (← 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)
• The genealogy, site frequency spectrum and ages of two nested mutant alleles (Q615607) (← links)
• Site frequency spectra from genomic SNP surveys (Q615623) (← links)
• Structured coalescent processes from a modified Moran model with large offspring numbers (Q615647) (← links)
• Selective sweeps for recessive alleles and for other modes of dominance (Q659034) (← links)
• The link between segregation and phylogenetic diversity (Q662584) (← links)
• The asymptotic distribution of the length of beta-coalescent trees (Q691115) (← links)
• Ancestral inference from haplotypes and mutations (Q725140) (← links)
• A non-zero variance of Tajima's estimator for two sequences even for infinitely many unlinked loci (Q725142) (← links)
• Editorial: Coalescent theory has many new branches (Q743257) (← links)
• Genotype imputation in a coalescent model with infinitely-many-sites mutation (Q743265) (← links)
• Theory and applications of a deterministic approximation to the coalescent model (Q743522) (← links)
• A numerical method for calculating moments of coalescent times in finite populations with selection (Q752044) (← links)
• Genealogy of neutral genes in two partially isolated populations (Q752046) (← links)
• First and second moments and the mean Hamming distance in a stochastic replication-mutation model for biological macromolecules (Q752580) (← links)
• Genealogical-tree probabilities in the infinitely-many-site model (Q753709) (← links)
• Line-of-descent and genealogical processes, and their applications in population genetics models (Q761376) (← links)
• A note on distributions of times to coalescence, under time-dependent population size (Q849458) (← links)
• Maximum likelihood and Bayesian methods for estimating the distribution of selective effects among classes of mutations using DNA polymorphism data (Q849468) (← links)
• A simple method for computing exact probabilities of mutation numbers (Q851379) (← links)
• Asymptotic results on the length of coalescent trees (Q930674) (← links)
• Analytical plug-in method for kernel density estimator applied to genetic neutrality study (Q939615) (← links)
• Neutral two-locus multiple allele models with recombination (Q1050280) (← links)
• Allele frequencies in a multidimensional Wright-Fisher model with general mutation (Q1052262) (← links)
• Estimation of the neutral mutation rate in a finite population from DNA sequence data (Q1053639) (← links)
• The use of sample genealogies for studying a selectively neutral m-loci model with recombination (Q1061645) (← links)
• Biased intrachromosomal gene conversion in a chromosome lineage (Q1068015) (← links)
• Homozygosity in a population of variable size and mutation rate (Q1068016) (← links)
• On the divergence of genes in multigene families (Q1086194) (← links)
• Diallelic multilocus model of neutral genes (Q1090641) (← links)
• Counting genealogical trees (Q1107468) (← links)
• Lines of descent in the diffusion approximation of neutral Wright-Fisher models (Q1140050) (← links)
• The number of heterozygous loci between two randomly chosen completely linked sequences of loci in two subdivided population models (Q1150328) (← links)
• A note on the sampling theory for infinite alleles and infinite sites models (Q1211426) (← links)
• Distribution of nucleotide differences between two randomly chosen cistrons in a subdivided population: The finite island model (Q1230750) (← links)
• Distribution of nucleotide differences between two randomly chosen cistrons in a population of variable size (Q1235083) (← links)
• Probability of a segregating pattern in a sample of DNA sequences (Q1268330) (← links)
• Maximum likelihood estimation of population divergence times and population phylogenies under the infinite sites model (Q1269434) (← links)
• Segregating sites in Wright's island model (Q1269439) (← links)