Evidence map›Paper›PMID 40956867›Full record

ArticlePLoS genetics2025

Jointly representing long-range genetic similarity and spatially heterogeneous isolation-by-distance.

Vivaswat Shastry, Marco Musiani, John Novembre

Abstract read
In one paragraph

Article in PLoS genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Vivaswat ShastryCommittee on Genetics, Genomics and Systems Biology, University of Chicago, Chicago, Illinois, United States of America.ORCID https://orcid.org/0000-0002-7294-5607
Marco MusianiDepartment of Biological, Geological, and Environmental Sciences, University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-6097-5841
John NovembreDepartment of Human Genetics, University of Chicago, Chicago, Illinois, United States of America.ORCID https://orcid.org/0000-0001-5345-0214

Funding

Theory, Methods, and Resources for Understanding and Leveraging Spatial Variation in Population Genetic DataR35GM149521 · NIGMS · UNIVERSITY OF CHICAGO · PI John Novembre · 2023 to 2026
$1.7M
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 GM132383NIGMS NIH HHS R35 GM149521
6 · The paper itself

Abstract

Isolation-by-distance patterns in genetic variation are a widespread feature of the geographic structure of genetic variation in many species, and many methods have been developed to illuminate such patterns in genetic data. However, long-range genetic similarities also exist, often as a result of rare or episodic long-range gene flow. Jointly characterizing patterns of isolation-by-distance and long-range genetic similarity in genetic data is an open data analysis challenge that, if resolved, could help produce more complete representations of the geographic structure of genetic data in any given species. Here, we present a computationally tractable method that identifies long-range genetic similarities in a background of spatially heterogeneous isolation-by-distance variation. The method uses a coalescent-based framework, and models long-range genetic similarity in terms of directional events with source fractions describing the fraction of ancestry at a location tracing back to a remote source. The method produces geographic maps annotated with inferred long-range edges, as well as maps of uncertainty in the geographic location of each source of long-range gene flow. We have implemented the method in a package called FEEMSmix (an extension to FEEMS), and validated its implementation using simulations representative of typical data applications. We also apply this method to two empirical data sets. In a data set of over 4,000 humans (Homo sapiens) across Afro-Eurasia, we recover many known signals of long-distance dispersal from recent centuries. Similarly, in a data set of over 100 gray wolves (Canis lupus) across North America, we identify several previously unknown long-range connections, some of which were attributable to recording errors in sampling locations. Therefore, beyond identifying genuine long-range dispersals, our approach also serves as a useful tool for quality control in spatial genetic studies.

Indexed as

Gene FlowGenetics, PopulationGenetic VariationModels, GeneticAnimalsHumansWolves

Identifiers

PMID40956867
PMCPMC12453258

What Socratic 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 Socratic graph.