Evidence map›Paper›PMID 32763953›Full record

ArticleG3 (Bethesda, Md.)2020

On the Distribution of Tract Lengths During Adaptive Introgression.

Vladimir Shchur, Jesper Svedberg, Paloma Medina, Russell Corbett-Detig, Rasmus Nielsen

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Human genetic admixture through the lens of population genomics.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  8. Article
  9. Review
  10. The history and evolution of the Denisovan-Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Article
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

5 authors.

Vladimir ShchurDepartment of Integrative Biology and Department of Statistics, UC Berkeley, Berkeley, CA vshchur@hse.ru.ORCID 0000-0002-1431-5260
Jesper SvedbergDepartment of Biomolecular Engineering and Genomics Institute, UC Santa Cruz, California 95064.ORCID 0000-0002-0951-3019
Paloma MedinaDepartment of Biomolecular Engineering and Genomics Institute, UC Santa Cruz, California 95064.ORCID 0000-0001-6760-3525
Russell Corbett-DetigNational Research University Higher School of Economics, Russian Federation.ORCID 0000-0001-6535-2478
Rasmus NielsenDepartment of Integrative Biology and Department of Statistics, UC Berkeley, Berkeley, CA.ORCID 0000-0003-0513-6591

Funding

Origins, Functional, and Evolutionary Consequences of Genomic VariationR35GM128932 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI Russell Corbett-Detig · 2018 to 2026
$3.2M
The Dynamics of Mitochondrial MutationsR01GM116044 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI MAKOVA, KATERYNA, NIELSEN, RASMUS · 2015 to 2018
$2.4M
UC Santa Cruz Training Program In Genomic SciencesT32HG008345 · NHGRI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI BROOKS, ANGELA NORIE, GREEN, RICHARD EDWARD · 2015 to 2020
$1.4M
NHGRI NIH HHS T32 HG008345NIGMS NIH HHS R01 GM116044NIGMS NIH HHS R35 GM128932
6 · The paper itself

Abstract

Admixture is increasingly being recognized as an important factor in evolutionary genetics. The distribution of genomic admixture tracts, and the resulting effects on admixture linkage disequilibrium, can be used to date the timing of admixture between species or populations. However, the theory used for such prediction assumes selective neutrality despite the fact that many famous examples of admixture involve natural selection acting for or against admixture. In this paper, we investigate the effects of positive selection on the distribution of tract lengths. We develop a theoretical framework that relies on approximating the trajectory of the selected allele using a logistic function. By numerically calculating the expected allele trajectory, we also show that the approach can be extended to cases where the logistic approximation is poor due to the effects of genetic drift. Using simulations, we show that the model is highly accurate under most scenarios. We use the model to show that positive selection on average will tend to increase the admixture tract length. However, perhaps counter-intuitively, conditional on the allele frequency at the time of sampling, positive selection will actually produce shorter expected tract lengths. We discuss the consequences of our results in interpreting the timing of the introgression of

Indexed as

Genetic DriftSelection, GeneticAllelesGene FrequencyGenetics, PopulationLinkage Disequilibriumadaptationadaptive introgressionadmixtureEPAS1selectiontract length

Identifiers

PMID32763953
PMCPMC7534438

What OpenQuestion holds

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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.