Evidence map›Paper›PMID 42282657›Full record

ArticlebioRxiv : the preprint server for biology2026

Causal inference clarifies the roles of background selection and mutation rate variation in shaping human genetic diversity.

Gustavo V Barroso, Nicholas W Collier, Chenlu Di, Kirk E Lohmueller, Aaron P Ragsdale

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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

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

5 authors.

Gustavo V BarrosoDepartment of Integrative Biology, University of Wisconsin-Madison, USA, 53706.ORCID 0000-0002-1943-9297
Nicholas W CollierDepartment of Integrative Biology, University of Wisconsin-Madison, USA, 53706.ORCID 0009-0005-0385-9798
Chenlu DiDepartment of Ecology and Evolutionary Biology, University of California-Los Angeles, USA, 90024.ORCID 0000-0002-7333-498X
Kirk E LohmuellerDepartment of Ecology and Evolutionary Biology, University of California-Los Angeles, USA, 90024.ORCID 0000-0002-3874-369X
Aaron P RagsdaleDepartment of Integrative Biology, University of Wisconsin-Madison, USA, 53706.ORCID 0000-0003-0715-3432

Funding

Population genomics of the selective effects of new mutationsR35GM119856 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LOHMUELLER, KIRK · 2016 to 2025
$3.4M
Population genetics of human evolutionary history and natural selectionR35GM154962 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Aaron Ragsdale · 2024 to 2026
$1.1M
NIGMS NIH HHS R35 GM119856NIGMS NIH HHS R35 GM154962
6 · The paper itself

Abstract

Decades of theoretical and empirical work have struggled to reconcile competing views on how evolution shapes patterns of genetic variation. We now understand the genome as a mosaic molded by both neutral and selective forces, but quantifying their relative contributions remains an open challenge. A major obstacle has been the tendency to analyze each evolutionary process in isolation. But different processes may leave similar signatures on genetic variation, making it challenging to draw conclusions from correlations alone. To address this gap, we make predictions of the landscape of diversity based on background selection and mutation rate variation. We then develop structural equation models describing how mutation, recombination and selection jointly shape the genomic landscape of diversity. This approach offers a more realistic representation of biological interactions and enables rigorous evaluation of hypothesized causal structures, marking both conceptual and practical improvements over previous studies. Analyses of human data reveal large variation in the explanatory power of candidate models across chromosomes. We find that previous studies likely overestimated the predictive accuracy of background selection; although it emerges as the overall main driver of diversity, in some chromosomes mutation rate variation has a comparable impact. We also show that recombination increases diversity more strongly through its influence on background selection than through its mutagenic effect, resolving a longstanding debate. This work demonstrates that modeling variation inherent in genome biology substantially improves our ability to explain human genetic diversity. At the same time, evidence for unmodeled covariance between mutation rates and density of constrained sites reinvigorates an ongoing discussion about the evolution of the mutation landscape, although additional work is needed to determine its origins.

Identifiers

PMID42282657
PMCPMC13252004

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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.