Evidence map›Paper›PMID 41673117›Full record

ArticleScientific reports2026

rhinotypeR enables reproducible rhinovirus genotype assignment from VP4/2 sequences.

Martha M Luka, Ruth Nanjala, Wafaa M Rashed, Winfred Gatua, Olaitan I Awe

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.

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0citing papers in PubMed
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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.

Martha M LukaSchool of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, G12 8QQ, UK.
Ruth NanjalaKennedy Institute of Rheumatology, Nuttfield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.
Wafaa M RashedPharmacy Practice Department, Faculty of Pharmacy, Ahram Canadian University, 6th October City, Egypt. wafaaanor@gmail.com.
Winfred GatuaMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Olaitan I AweInstitute for Genomic Medicine Research, West Hartford, CT, USA. laitanawe@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rhinoviruses (RVs) are among the most prevalent human respiratory pathogens, yet their molecular characterization remains fragmented across analytical tools and inconsistent between studies. Current genotype assignment typically relies on sequence alignment, pairwise distance calculation, and prototype comparison. This fragmentation hinders reproducibility and scalability. Here, we present rhinotypeR, an open-source R package that provides a scriptable and transparent workflow for RV genotyping based on the VP4/2 genomic region. The package integrates multiple analytical steps; alignment, distance calculation, genotype assignment, and visualization within the Bioconductor ecosystem and applies standardized species-specific thresholds (10.5% for HRV-A/C and 9.5% for HRV-B). Using a validation dataset encompassing over 90% of known RV types, rhinotypeR reproduced pairwise genetic distances obtained with ape and MEGA X with Mantel correlation (r = 1.000, p = 0.001) and negligible numerical deviation (< 10⁻

Indexed as

Capsid ProteinsRhinovirusSoftwareGenome, ViralGenotypeHumansPhylogenyReproducibility of ResultsCapsid ProteinsVP2 protein, RhinovirusBioconductorrhinotypeRRhinovirusR packageVP4/2 genotype

Identifiers

PMID41673117
PMCPMC12901022

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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.