Evidence map›Paper›PMID 40502143›Full record

ArticlebioRxiv : the preprint server for biology2025

Fine-Resolution Asymmetric Migration Estimation.

Hao Shen, John Novembre

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing 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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Hao ShenDepartment of Human Genetics, University of Chicago.
John NovembreDepartment of Human Genetics, University of Chicago.

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
NIGMS NIH HHS R35 GM149521
6 · The paper itself

Abstract

The genetic structure of populations is often shaped by processes and events that introduce asymmetries to gene flow between geographic locations. Existing population genetic methods like EEMS and FEEMS summarize gene flow using effective equilibrium migration rates that are assumed to be symmetric, providing representations of underlying structure that have proven useful, but that fail short of representing signatures of aysmmetric gene flow. More elaborate methods capable of inferring asymmetric gene flow exist, but are computationally intensive, restricting analyses to small sets of sub-populations (demes). Here, we introduce FRAME (Fine-Resolution Asymmetric Migration Estimation), a method that significantly reduces the computational burden of estimating asymmetric gene flow. This efficiency allows FRAME to infer asymmetric migration patterns for scenarios with a large number of demes, enabling fine-scale analyses. Under the assumed model and its equilibrium condition, FRAME's estimates can be interpreted as backward migration rates; in non-equilibrium conditions, FRAME detects and summarizes asymmetries in gene flow with effective equilibrium migration rates, which allows a richer representation of genetic structure. We assess the method using a variety of simulated histories of gene flow and apply the method to datasets from North American gray wolves, poplar trees, white-crowned mannakin, and human archaeogenetic samples. The applications demonstrate FRAME's scalability and flexibility in detecting complex asymmetric migration signals and population structures.

Identifiers

PMID40502143
PMCPMC12154593

What Socratic holds

Textmetadata
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.