Evidence map›Paper›PMID 41279849›Full record

ArticlebioRxiv : the preprint server for biology2025

Analytical expectations for ancestry junction accumulation in admixed genomes.

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

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.

0numbers the graph read from it
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

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

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

5 authors.

Shirin NataneliDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA, USA.ORCID 0000-0001-7880-9967
Aydin Loid KaratasDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA, USA.ORCID 0009-0007-2676-9968
Roshni A PatelDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA, USA.ORCID 0000-0002-8574-031X
Tessa FerrariDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA, USA.ORCID 0009-0009-7692-4465
Jazlyn A MooneyDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA, USA.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 GM137758NIGMS NIH HHS R35 GM159982
6 · The paper itself

Abstract

Complex demographic events have shaped human history, leaving signatures of genetic variation across the genome. Here, we recover the recent evolutionary history of admixed populations formed from multiple 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, and extend these expectations to incorporate population-specific recombination maps. Forward-time simulations tracing ancestry junctions for ten generations after admixture show close agreement with theoretical predictions under constant and variable recombination models. We observe minimal variability in switch counts across ten replicates, underscoring the robustness of the theoretical expectation. Furthermore, model-based switch counts 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 reconstruct how recombination and demography jointly shape ancestry patterns in admixed populations without requiring separation into parental sources.

Identifiers

PMID41279849
PMCPMC12636454

What Socratic holds

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LicenceCC BY-NC
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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.