Evidence map›Paper›PMID 26311475›Full record

ArticleGenetics2015

A Coalescent Model for a Sweep of a Unique Standing Variant.

Jeremy J Berg, Graham Coop

Abstract read
In one paragraph

Article in Genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed.

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  20. Population genomics perspectives on convergent adaptation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
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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

2 authors.

Jeremy J BergGraduate Group in Population Biology, University of California, Davis, California 95616 Center for Population Biology, University of California, Davis, California 95616 Department of Evolution and Ecology, University of California, Davis, California 95616 jjberg@ucdavis.edu gmcoop@ucdavis.edu.
Graham CoopCenter for Population Biology, University of California, Davis, California 95616 Department of Evolution and Ecology, University of California, Davis, California 95616 jjberg@ucdavis.edu gmcoop@ucdavis.edu.

Funding

Recombination rate variation and evolution in vertebratesR01GM083098 · NIGMS · UNIVERSITY OF CHICAGO · PI PRZEWORSKI, MOLLY F · 2007 to 2024
$4.6M
Genome-wide approaches to polygenic adaptationR01GM108779 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI COOP, GRAHAM · 2014 to 2019
$1.0M
NIGMS NIH HHS R01 GM083098NIGMS NIH HHS R01GM107374NIGMS NIH HHS R01 GM108779NIGMS NIH HHS R01GM83098
6 · The paper itself

Abstract

The use of genetic polymorphism data to understand the dynamics of adaptation and identify the loci that are involved has become a major pursuit of modern evolutionary genetics. In addition to the classical "hard sweep" hitchhiking model, recent research has drawn attention to the fact that the dynamics of adaptation can play out in a variety of different ways and that the specific signatures left behind in population genetic data may depend somewhat strongly on these dynamics. One particular model for which a large number of empirical examples are already known is that in which a single derived mutation arises and drifts to some low frequency before an environmental change causes the allele to become beneficial and sweeps to fixation. Here, we pursue an analytical investigation of this model, bolstered and extended via simulation study. We use coalescent theory to develop an analytical approximation for the effect of a sweep from standing variation on the genealogy at the locus of the selected allele and sites tightly linked to it. We show that the distribution of haplotypes that the selected allele is present on at the time of the environmental change can be approximated by considering recombinant haplotypes as alleles in the infinite-alleles model. We show that this approximation can be leveraged to make accurate predictions regarding patterns of genetic polymorphism following such a sweep. We then use simulations to highlight which sources of haplotypic information are likely to be most useful in distinguishing this model from neutrality, as well as from other sweep models, such as the classic hard sweep and multiple-mutation soft sweeps. We find that in general, adaptation from a unique standing variant will likely be difficult to detect on the basis of genetic polymorphism data from a single population time point alone, and when it can be detected, it will be difficult to distinguish from other varieties of selective sweeps. Samples from multiple populations and/or time points have the potential to ease this difficulty.

Indexed as

Evolution, MolecularGenetics, PopulationSelection, GeneticAdaptation, PhysiologicalAllelesHaplotypesHumansModels, GeneticMutationPolymorphism, Geneticcoalescent theorygenetic hitchhikingnatural selectionsoft sweepstanding variation

Identifiers

PMID26311475
PMCPMC4596678

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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.