Evidence map›Paper›PMID 41936602›Full record

ArticleScientific reports2026

Predicting the evolution and persistence of COVID-19 using context-dependent polymorphisms.

John Caraway, Way Sung

Abstract read
In one paragraph

Article in Scientific reports, 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

2 authors.

John CarawayDepartment of Bioinformatics and Genomics, University of North Carolina Charlotte, North Carolina, Charlotte, 28269, USA.
Way SungDepartment of Bioinformatics and Genomics, University of North Carolina Charlotte, North Carolina, Charlotte, 28269, USA. wsung@charlotte.edu.

Funding

NSF 1818125
6 · The paper itself

Abstract

Identifying common patterns of polymorphisms across SARS-CoV-2 variants is an essential part of tracking and preventing future pandemics. By examining the large-scale global sequencing effort of SARS-CoV-2, we find that polymorphisms in SARS-CoV-2 are context-dependent and significantly correlated across different variants, with neighboring nucleotides capable of altering polymorphism frequency by an average of 72-fold. Incorporating context-dependent patterns into evolutionary simulations improves the ability to predict polymorphisms in SARS-CoV-2 by 94%, and reveal relatively immutable regions in NSP3, NSP13, and the spike protein that are potential targets for gene therapy. Subdividing SARS-CoV-2 into Persistent and Transient variants reveal that Persistent variants carry an excess of unique polymorphisms in the hand domain of the RNA-dependent RNA polymerase (p = 0.001). Overall, our work highlights the importance of context-dependent polymorphisms in the evolution of the SARS-CoV-2 genome, associates genetic signatures with variant persistence, and identifies static regions and motifs that can be used to design long-lasting antivirals that rely on sequence specificity.

Indexed as

COVID-19Evolution, MolecularPolymorphism, GeneticSARS-CoV-2Genome, ViralHumansRNA-Dependent RNA PolymeraseSpike Glycoprotein, CoronavirusViral Nonstructural ProteinsRNA-Dependent RNA PolymeraseSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Viral Nonstructural Proteins

Identifiers

PMID41936602
PMCPMC13216584

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.