Evidence map›Paper›PMID 30963935›Full record

ArticleProceedings. Biological sciences2019

Inferring the model and onset of natural selection under varying population size from the site frequency spectrum and haplotype structure.

Shigeki Nakagome, Richard R Hudson, Anna Di Rienzo

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Article in Proceedings. Biological sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Shigeki Nakagome1 Department of Human Genetics, University of Chicago , Chicago, IL , USA.
Richard R Hudson1 Department of Human Genetics, University of Chicago , Chicago, IL , USA.
Anna Di Rienzo1 Department of Human Genetics, University of Chicago , Chicago, IL , USA.

Funding

Evolutionary genomics of the vitamin D pathway in humans - Resubmission 01R01GM101682 · NIGMS · UNIVERSITY OF CHICAGO · PI DI RIENZO, ANNA · 2012 to 2015
$1.2M
NIGMS NIH HHS R01 GM101682
6 · The paper itself

Abstract

A fundamental question about adaptation in a population is the time of onset of the selective pressure acting on beneficial alleles. Inferring this time, in turn, depends on the selection model. We develop a framework of approximate Bayesian computation (ABC) that enables the use of the full site frequency spectrum and haplotype structure to test the goodness-of-fit of selection models and estimate the timing of selection under varying population size scenarios. We show that our method has sufficient power to distinguish natural selection from neutrality even if relatively old selection increased the frequency of a pre-existing allele from 20% to 50% or from 40% to 80%. Our ABC can accurately estimate the time of onset of selection on a new mutation. However, estimates are prone to bias under the standing variation model, possibly due to the uncertainty in the allele frequency at the onset of selection. We further extend our approach to take advantage of ancient DNA data that provides information on the allele frequency path of the beneficial allele. Applying our ABC, including both modern and ancient human DNA data, to four pigmentation alleles in Europeans, we detected selection on standing variants that occurred after the dispersal from Africa even though models of selection on a new mutation were initially supported for two of these alleles without the ancient data.

Indexed as

Gene FrequencyHuman MigrationSelection, GeneticBayes TheoremDNA, AncientEuropeHaplotypesHumansModels, GeneticPopulation DensitySkin PigmentationTime FactorsDNA, Ancientapproximate Bayesian computationnatural selection on standing variationselective sweeptiming of natural selection

Identifiers

PMID30963935
PMCPMC6408616

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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.