Evidence map›Paper›PMID 29574050›Full record

ArticleTheoretical population biology2018

Inference from the stationary distribution of allele frequencies in a family of Wright-Fisher models with two levels of genetic variability.

Jake M Ferguson, Erkan Ozge Buzbas

Abstract read
In one paragraph

Article in Theoretical population biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Jake M FergusonCenter for Modeling Complex Interactions, University of Idaho, United States.
Erkan Ozge BuzbasDepartment of Statistical Science, University of Idaho, United States. Electronic address: erkanb@uidaho.edu.

Funding

Sequence-structure-function relationships in human visual photopigmentsP20GM104420 · NIGMS · UNIVERSITY OF IDAHO · PI WICHMAN, HOLLY A · 2015 to 2024
$22.9M
NIGMS NIH HHS P20 GM104420
6 · The paper itself

Abstract

The distribution of allele frequencies obtained from diffusion approximations to Wright-Fisher models is useful in developing intuition about the population level effects of evolutionary processes. The statistical properties of the stationary distributions of K-allele models have been extensively studied under neutrality or under selection. Here, we introduce a new family of Wright-Fisher models in which there are two hierarchical levels of genetic variability. The genotypes composed of alleles differing from each other at the selected level have fitness differences with respect to each other and evolve under selection. The genotypes composed of alleles differing from each other only at the neutral level have the same fitness and evolve under neutrality. We show that with an appropriate scaling of the mutation parameter with respect to the number of alleles at each level, the frequencies of alleles at the selected and the neutral level are conditionally independent of each other, conditional on knowing the number of alleles at all levels. This conditional independence allows us to simulate from the joint stationary distribution of the allele frequencies. We use these simulated frequencies to perform inference on parameters of the model with two levels of genetic variability using Approximate Bayesian Computation.

Indexed as

Gene FrequencyGenetics, PopulationModels, GeneticSelection, GeneticAlgorithmsAllelesBayes TheoremBiological EvolutionComputer SimulationGenetic DriftGenotypeHumansMutation-allele modelsApproximate Bayesian ComputationBalancing selectionDiffusion approximationWright–Fisher model

Identifiers

PMID29574050
PMCPMC6054576

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.