Evidence map›Paper›PMID 36537881›Full record

ArticleeLife2022

Modeling the spatiotemporal spread of beneficial alleles using ancient genomes.

Rasa A Muktupavela, Martin Petr, Laure Ségurel, Thorfinn Korneliussen, John Novembre, Fernando Racimo

Abstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Ancient DNA and Human Physiology.Physiology (Bethesda, Md.) · 2026
    Review
  2. Review
  3. Article
  4. Resource-explicit interactions in spatial population models.Methods in ecology and evolution · 2024
    Article
  5. Peer community journal · 2023
    Article
  6. Review
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

6 authors.

Rasa A MuktupavelaLundbeck GeoGenetics Centre, GLOBE Institute, Faculty of Health, Copenhagen, Denmark.ORCID 0000-0001-5590-5948
Martin PetrLundbeck GeoGenetics Centre, GLOBE Institute, Faculty of Health, Copenhagen, Denmark.ORCID 0000-0003-4879-8421
Laure SégurelUMR5558 Biométrie et Biologie Evolutive, CNRS - Université Lyon 1, Villeurbanne, France.ORCID 0000-0001-7339-0976
Thorfinn KorneliussenLundbeck GeoGenetics Centre, GLOBE Institute, Faculty of Health, Copenhagen, Denmark.
John NovembreDepartment of Human Genetics, University of Chicago, Chicago, United States.ORCID 0000-0001-5345-0214
Fernando RacimoLundbeck GeoGenetics Centre, GLOBE Institute, Faculty of Health, Copenhagen, Denmark.ORCID 0000-0002-5025-2607

Funding

Extending Tools for Visualization of Geographic Structure in Population Genomic DataR01GM132383 · NIGMS · UNIVERSITY OF CHICAGO · PI NOVEMBRE, JOHN · 2019 to 2022
$1.4M
NIGMS NIH HHS R01 GM132383
6 · The paper itself

Abstract

Ancient genome sequencing technologies now provide the opportunity to study natural selection in unprecedented detail. Rather than making inferences from indirect footprints left by selection in present-day genomes, we can directly observe whether a given allele was present or absent in a particular region of the world at almost any period of human history within the last 10,000 years. Methods for studying selection using ancient genomes often rely on partitioning individuals into discrete time periods or regions of the world. However, a complete understanding of natural selection requires more nuanced statistical methods which can explicitly model allele frequency changes in a continuum across space and time. Here we introduce a method for inferring the spread of a beneficial allele across a landscape using two-dimensional partial differential equations. Unlike previous approaches, our framework can handle time-stamped ancient samples, as well as genotype likelihoods and pseudohaploid sequences from low-coverage genomes. We apply the method to a panel of published ancient West Eurasian genomes to produce dynamic maps showcasing the inferred spread of candidate beneficial alleles over time and space. We also provide estimates for the strength of selection and diffusion rate for each of these alleles. Finally, we highlight possible avenues of improvement for accurately tracing the spread of beneficial alleles in more complex scenarios.

Indexed as

Selection, GeneticAllelesGene FrequencyHumansancient DNAdiffusionevolutionevolutionary biologyhumanlactase persistencenatural selectionspatiotemporal inference

Identifiers

PMID36537881
PMCPMC9767474

What OpenQuestion holds

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LicenceCC BY
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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.