Evidence map›Paper›PMID 41674715›Full record

ArticleQuantitative biology (Beijing, China)2025

A data-driven sliding-window pairwise comparative approach for the estimation of transmission fitness of SARS-CoV-2 variants and construction of the evolution fitness landscape.

Md Jubair Pantho, Richard Annan, Landen Alexander Bauder, Sophia Huang, Letu Qingge, Hong Qin

Abstract read
In one paragraph

Article in Quantitative biology (Beijing, China), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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.

Md Jubair PanthoDepartment of Computer Science and Engineering University of Tennessee at Chattanooga Chattanooga Tennessee USA.ORCID https://orcid.org/0009-0002-8874-8154
Richard AnnanDepartment of Computer Science North Carolina Agricultural and Technical State University Greensboro North Carolina USA.
Landen Alexander BauderDepartment of Computer Science and Engineering University of Tennessee at Chattanooga Chattanooga Tennessee USA.
Sophia HuangThomas Jefferson High School for Science and Technology Alexandria Virginia USA.
Letu QinggeDepartment of Computer Science North Carolina Agricultural and Technical State University Greensboro North Carolina USA.
Hong QinDepartment of Computer Science and Engineering University of Tennessee at Chattanooga Chattanooga Tennessee USA.ORCID https://orcid.org/0000-0002-1060-6722

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Estimating the transmission fitness of SARS-CoV-2 variants and understanding their evolutionary fitness trends are important for epidemiological forecasting. Existing methods are often constrained by their parametric natures and do not satisfactorily align with the observations during COVID-19. Here, we introduce a sliding-window data-driven pairwise comparison method, the differential population growth rate (DPGR) that uses viral strains as internal controls to mitigate sampling biases. DPGR is applicable in time windows in which the logarithmic ratio of two variant subpopulations is approximately linear. We apply DPGR to genomic surveillance data and focus on variants of concern (VOCs) in multiple countries and regions. We found that the log-linear assumption of DPGR can be reliably found within appropriate time windows in many areas. We show that DPGR estimates of VOCs align well with regional empirical observations in different countries. We show that DPGR estimates agree with another method for estimating pathogenic transmission. Furthermore, DPGR allowed us to construct viral relative fitness landscapes that capture the shifting trends of SARS-CoV-2 evolution, reflecting the relative changes of transmission traits for key genotypic changes represented by major variants. The straightforward log-linear regression approach of DPGR may also facilitate its easy adoption. This study shows that DPGR is a promising new tool in our repertoire for addressing future pandemics.

Indexed as

fitness landscapepairwise comparative estimationSARS‐CoV‐2sliding‐windowsviral variant fitness

Identifiers

PMID41674715
PMCPMC12806054

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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.