Evidence map›Paper›PMID 21575649›Full record

ArticleTheoretical population biology2011

Genetic diversity of microsatellite loci in hierarchically structured populations.

Seongho Song, Dipak K Dey, Kent E Holsinger

Abstract read
In one paragraph

Article in Theoretical population biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Seongho SongDepartment of Mathematical Sciences, University of Cincinnati, ML:210025, Cincinnati, OH 45221-0025, USA. seongho.song@uc.edu
Dipak K Dey
Kent E Holsinger

Funding

Bayesian methods for analyzing genetic diversityR01GM068449 · NIGMS · UNIVERSITY OF CONNECTICUT STORRS · PI HOLSINGER, KENT E · 2004 to 2006
$355k
NIGMS NIH HHS 1 R01 GM068449-01A1NIGMS NIH HHS R01 GM068449
6 · The paper itself

Abstract

Microsatellite loci are widely used for investigating patterns of genetic variation within and among populations. Those patterns are in turn determined by population sizes, migration rates, and mutation rates. We provide exact expressions for the first two moments of the allele frequency distribution in a stochastic model appropriate for studying microsatellite evolution with migration, mutation, and drift under the assumption that the range of allele sizes is bounded. Using these results, we study the behavior of several measures related to Wright's F(ST), including Slatkin's R(ST). Our analytical approximations for F(ST) and R(ST) show that familiar relationships between N(e)m and F(ST) or R(ST) hold when the migration and mutation rates are small. Using the exact expressions for F(ST) and R(ST), our numerical results show that, when the migration and mutation rates are large, these relationships no longer hold. Our numerical results also show that the diversity measures most closely related to F(ST) depend on mutation rates, mutational models (stepwise versus two-phase), migration rates, and population sizes. Surprisingly, R(ST) is relatively insensitive to the mutation rates and mutational models. The differing behaviors of R(ST) and F(ST) suggest that properties of the among-population distribution of allele frequencies may allow the roles of mutation and migration in producing patterns of diversity to be distinguished, a topic of continuing investigation.

Indexed as

Biological EvolutionGenetic VariationMicrosatellite RepeatsModels, GeneticAnimalsGenetic DriftGenetic LociGenetics, PopulationHumansMutation

Identifiers

PMID21575649
PMCPMC3124608

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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.