Evidence map›Paper›PMID 41789724›Full record

ArticleGenetics2026

Analytical expectations for ancestry junction accumulation in admixed genomes.

Shirin Nataneli, Aydin Loid Karatas, Tessa Ferrari, Roshni A Patel, Jazlyn A Mooney

Abstract read
In one paragraph

Article in Genetics, 2026. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Shirin NataneliDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA 90089, United States.ORCID 0000-0001-7880-9967
Aydin Loid KaratasDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA 90089, United States.ORCID 0009-0007-2676-9968
Tessa FerrariDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA 90089, United States.ORCID 0009-0009-7692-4465
Roshni A PatelDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA 90089, United States.ORCID 0000-0002-8574-031X
Jazlyn A MooneyDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA 90089, United States.ORCID 0000-0002-2369-0855

Funding

Traits on trees: Population genomics for understanding complex phenotypesR35GM137758 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Michael Donald Edge · 2020 to 2026
$2.5M
Population Genomics Across Global Populations: Flexible Methods for Inference and Detecting Rare Recessive VariationR35GM159982 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Jazlyn Ambry Mooney · 2025 to 2026
$802k
NIGMS NIH HHS R35 GM159982NIH HHS R35GM137758NIH HHS R35GM159982
6 · The paper itself

Abstract

Complex demographic events have shaped human history, leaving signatures of genetic variation across the genome. Here, we investigate the recent evolutionary dynamics of admixed populations that descend from distinct ancestral sources. We present a discrete, generalizable model of admixture that leverages ancestry switches, which are recombination breakpoints that mark changes in ancestral origin along a chromosome. We derive analytical expectations for the number of ancestry switches within a genomic segment as functions of recombination rate, ancestry heterozygosity, and effective population size. We then extend these expectations to incorporate population-specific recombination maps. Our theoretical predictions are in close agreement with forward-in-time simulations that trace ancestry junction accumulation following an initial admixture event under both constant and variable recombination models. We observe minimal variability in switch counts across ten simulation replicates, underscoring the robustness of the theoretical expectation. Furthermore, model-based switch counts, parameterized using literature-informed demographic values, agree with empirical observations from African-American individuals in the 1000 Genomes Project. For example, when modeling human chromosome 1, we found a mean of approximately six switches per haplotype, which aligns with the theoretical expectation under an initial African ancestry proportion of 0.85 and agrees with published estimates from other African-American cohorts. Overall, the model provides a new route for using ancestry switches to understand how recombination and demography jointly shape ancestry patterns in admixed populations without requiring separation into parental sources.

Indexed as

Genetics, PopulationGenome, HumanModels, GeneticBlack or African AmericanEvolution, MolecularGenetic VariationHaplotypesHumansRecombination, Geneticadmixtureancestry junctionsPEQG2026population geneticsrecombination

Identifiers

PMID41789724
PMCPMC13232761

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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.