Evidence map›Paper›PMID 25840144›Full record

ArticleTheoretical population biology2015

Sensitivity of quantitative traits to mutational effects and number of loci.

Joshua G Schraiber, Michael J Landis

Abstract read
In one paragraph

Article in Theoretical population biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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.

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

13 citing papers in PubMed.

  1. Evolution of quantitative traits with background selection.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  10. Review
  11. Empirical measures of mutational effects define neutral models of regulatory evolution inProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  12. 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

2 authors.

Joshua G SchraiberDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, United States. Electronic address: schraib@uw.edu.
Michael J LandisDepartment of Integrative Biology, University of California, Berkeley, CA 94720, United States.

Funding

MODELS OF COMPLEX GENETIC SYSTEMSR01GM040282 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI SLATKIN, MONTGOMERY WILSON · 1988 to 2017
$4.4M
Extending Bayesian Phylogenetic AnalysisR01GM069801 · NIGMS · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI HUELSENBECK, JOHN P. · 2004 to 2013
$2.1M
NIGMS NIH HHS R01 GM040282NIGMS NIH HHS R01 GM069801NIGMS NIH HHS R01-GM069801NIGMS NIH HHS R01-GM40282
6 · The paper itself

Abstract

When models of quantitative genetic variation are built from population genetic first principles, several assumptions are often made. One of the most important assumptions is that traits are controlled by many genes of small effect. This leads to a prediction of a Gaussian trait distribution in the population, via the Central Limit Theorem. Since these biological assumptions are often unknown or untrue, we characterized how finite numbers of loci or large mutational effects can impact the sampling distribution of a quantitative trait. To do so, we developed a neutral coalescent-based framework, allowing us to gain a detailed understanding of how number of loci and the underlying mutational model impacts the distribution of a quantitative trait. Through both analytical theory and simulation we found the normality assumption was highly sensitive to the details of the mutational process, with the greatest discrepancies arising when the number of loci was small or the mutational kernel was heavy-tailed. In particular, skewed mutational effects will produce skewed trait distributions and fat-tailed mutational kernels result in multimodal sampling distributions, even for traits controlled by a large number of loci. Since selection models and robust neutral models may produce qualitatively similar sampling distributions, we advise extra caution should be taken when interpreting model-based results for poorly understood systems of quantitative traits.

Indexed as

Genetics, PopulationGenetic VariationHumansModels, GeneticMutationPhenotypeQuantitative Trait LociCharacteristic functionCoalescent theoryNeutral theoryQuantitative genetics

Identifiers

PMID25840144
PMCPMC4437879

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Registered trials

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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.