Evidence map›Paper›PMID 42679004›Full record

ArticlePLoS computational biology2026

From sequences to strategies: Early detection of new SARS-CoV-2 variants via genetic distance to reduce hospitalizations.

Marika D'Avanzo, Aung Pone Myint, Giacomo Cacciapaglia, Stefan Hohenegger, Francesco Conventi, Marta Nunes

Abstract read
In one paragraph

Article in PLoS computational 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.

Marika D'AvanzoPhD National Programme in One Health approaches to infectious diseases and life science research, Department of Public Health, Experimental and Forensic Medicine, University of Pavia, Pavia, Italy.ORCID 0009-0008-3624-3887
Aung Pone MyintCenter of Excellence in Respiratory Pathogens (CERP), Hospices Civils de Lyon (HCL) and Centre International de Recherche en Infectiologie (CIRI), Équipe Santé Publique, Épidémiologie et Écologie Évolutive des Maladies Infectieuses (PHE3ID), Inserm U1111, CNRS UMR5308, ENS de Lyon, Université Claude Bernard Lyon 1, Lyon, France.ORCID 0000-0002-5603-8724
Giacomo CacciapagliaLaboratoire de Physique Théorique et Hautes Energies (LPTHE), UMR, Sorbonne Université & CNRS, France.
Stefan HoheneggerUniversité Claude Bernard Lyon 1, CNRS/IN2P3, IP2I UMR 5822, Villeurbanne, France.
Francesco ConventiINFN Sezione di Napoli, Complesso Universitario di Monte S. Angelo Edificio 6, Naples, Italy.
Marta NunesCenter of Excellence in Respiratory Pathogens (CERP), Hospices Civils de Lyon (HCL) and Centre International de Recherche en Infectiologie (CIRI), Équipe Santé Publique, Épidémiologie et Écologie Évolutive des Maladies Infectieuses (PHE3ID), Inserm U1111, CNRS UMR5308, ENS de Lyon, Université Claude Bernard Lyon 1, Lyon, France.ORCID 0000-0003-3788-878X

Funding

French National Research Agency (ANR)NextGenerationEU-MUR PNRR Extended Partnership initiative on Emerging Infectious Diseases
6 · The paper itself

Abstract

The COVID-19 pandemic highlighted the critical need for robust methods to monitor viral evolution and detect emerging variants of concern (VOCs). This study expanded an unsupervised clustering algorithm, based on Levenshtein distance, to track and predict variant predominance across six European countries from 2020 to January 2024. We also investigated the influence of genetic distances and containment strategies on hospitalization rates. Spike protein sequences were transformed into temporal chains. A deep neural network (DNN) was trained to classify emerging chains as likely dominant, while a CatBoost model assessed important variables, and simulations explored modifying vaccine genetic distance, containment measures, and vaccination coverage. Approximately 5,000 sequences per week enabled early chain detection within four weeks. The DNN achieved high classification performance for identifying future predominant chains within 3-4 weeks of detection. Genetic distance metrics between consecutive chains and between circulating and vaccine strains were among the most informative variables associated with hospitalization patterns. Model-based simulations suggested that scenarios involving improved vaccine matching or stronger containment measures were associated with lower predicted hospitalization burdens. Doubling vaccination coverage alone had minimal effect but showed additional reductions when combined with strict containment. Our findings from this integrated framework highlight the potential relevance of genetic distance metrics and public health interventions when assessing hospitalization risk associated with emerging variants.

Indexed as

COVID-19HospitalizationSARS-CoV-2Clustering AlgorithmsComputational BiologyComputer SimulationCOVID-19 VaccinesEuropeHumansNeural Networks, ComputerPandemicsSpike Glycoprotein, CoronavirusCOVID-19 VaccinesSpike Glycoprotein, Coronavirus

Identifiers

PMID42679004
PMCPMC13577520

What OpenQuestion holds

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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.