Evidence map›Paper›PMID 42395539›Full record

ArticlebioRxiv : the preprint server for biology2026

Variation and selection at predicted G-quadruplexes across the human pangenome.

Saswat K Mohanty, Maximillian G Marin, Linnéa Smeds, Francesca Chiaromonte, Christian D Huber, Kateryna D Makova

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

6 authors.

Saswat K MohantyMolecular, Cellular, and Integrative Biosciences, Huck Institutes of the Life Sciences, Penn State University, University Park, PA 16802, USA.ORCID 0000-0002-1813-589X
Maximillian G MarinDana Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.ORCID 0000-0002-9108-3328
Linnéa SmedsDepartment of Biology, Penn State University, University Park, PA 16802, USA.ORCID 0000-0002-8415-9259
Francesca ChiaromonteDepartment of Statistics, Penn State University, University Park, PA 16802, USA.
Christian D HuberDepartment of Biology, Penn State University, University Park, PA 16802, USA.ORCID 0000-0002-2267-2604
Kateryna D MakovaDepartment of Biology, Penn State University, University Park, PA 16802, USA.ORCID 0000-0002-6212-9526

Funding

The WashU-UCSC-EBI Human Genome Reference Center."U41HG010972 · NHGRI · WASHINGTON UNIVERSITY · PI Ira M Hall, Heng Li · 2019 to 2026
$24.9M
ELSI Administrative Supplement - Center for Human Reference Genome DiversityU01HG010971 · NHGRI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI EICHLER, EVAN, JARVIS, ERICH D · 2019 to 2023
$18.4M
Telomere-to-telomere assemblies of human genomesR01HG011274 · NHGRI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI Karen Hayden Miga · 2020 to 2026
$4.5M
Non-B DNA and Genome EvolutionR35GM151945 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI KATERYNA MAKOVA · 2024 to 2026
$2.6M
Tools for comprehensive variant characterization using the pangenomeU01HG013748 · NHGRI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI LI, HENG, MARSCHALL, TOBIAS · 2024 to 2024
$1.7M
Building Tools and Community to Make Pangenomes AccessibleU01HG013760 · NHGRI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI GARRISON, ERIK · 2024 to 2024
$1.6M
Tooling for accurately studying the epigenome along the human pangenome referenceU01HG013744 · NHGRI · UNIVERSITY OF WASHINGTON · PI STERGACHIS, ANDREW BEN · 2024 to 2024
$1.4M
Integrating the reference pangenome with biobank-scale data for complex trait analysisU01HG013755 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GYMREK, MELISSA · 2024 to 2024
$1.3M
NHGRI NIH HHS R01 HG011274NHGRI NIH HHS U01 HG010971NHGRI NIH HHS U01 HG013744NHGRI NIH HHS U01 HG013748NHGRI NIH HHS U01 HG013755NHGRI NIH HHS U01 HG013760NHGRI NIH HHS U41 HG010972NIGMS NIH HHS R35 GM151945
6 · The paper itself

Abstract

G-quadruplexes (G4s), non-canonical DNA structures whose sequence motifs occupy approximately 1% of the human genome, are important for myriad cellular functions, including regulating transcription and replication. Yet they also contribute to genomic instability by increasing mutations and structural variation. Despite their significance, G4 motifs have not been studied in detail across multiple human genomes. Here, we conducted a comprehensive analysis of presence/absence and sequence variation, measured selection strength, and evaluated gene expression regulation potential for predicted G4s (pG4s) across population groups in the second release of the Human Pangenome Reference Consortium dataset, comprising high-quality, near-telomere-to-telomere diploid genomes from 231 individuals worldwide, along with three reference assemblies. Across the human pangenome, we identified over 353 million pG4s, including 1.15 million pG4s absent from reference assemblies but shared across other haplotypes. Our analysis revealed that pG4 sharing patterns recapitulate human population structure: African individuals displayed lower levels of pG4 sharing than non-Africans, whereas East Asian individuals exhibited higher levels of sharing. By analyzing the site frequency spectrum across various genomic annotations, we computed and compared selection coefficients (

Identifiers

PMID42395539
PMCPMC13321086

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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 OpenQuestion graph.