Evidence map›Paper›PMID 40832913›Full record

ArticleJournal of medical virology2025

Development and Validation of Amplicon-Based Protocol for Sequencing of Respiratory Syncytial Virus Genome.

Guglielmo Ferrari, Great Romano, Antonino Maria Guglielmo Pitrolo, Fausto Baldanti, Antonio Piralla

Abstract readValidation Study
In one paragraph

Article in Journal of medical virology, 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

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

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

5 authors.

Guglielmo FerrariMicrobiology and Virology Department, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Great RomanoMicrobiology and Virology Department, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Antonino Maria Guglielmo PitroloMicrobiology and Virology Department, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Fausto BaldantiMicrobiology and Virology Department, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Antonio PirallaMicrobiology and Virology Department, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.

Funding

This study was supported by SURVEID Project, program 2022; Next Generation EU-MUR PNRR Extended Partnership initiative on Emerging Infectious Diseases (Project no. PE00000007, INF-ACT); and Fondo di Beneficenza of Intesa Sanpaolo S.p.A. (ID project B/2023/0181).
6 · The paper itself

Abstract

The most prevalent cause of severe respiratory infections in children is the human respiratory syncytial virus (RSV). The advent of next-generation sequencing (NGS) has made it possible to incorporate this technology into pathogen monitoring and surveillance. Whole-genome sequencing (WGS) of RSV has now become a relatively widely used method for tracking viral evolution. Here we report an improved high-throughput RSV-WGS assay performed directly on clinical samples that is suitable for short-read sequencing platforms. A total of 100 RSV-positive samples collected between November 2022 and March 2024 fulfilled the inclusion cycle quantification criteria and were randomly included in the validation process. The WGS protocol was designed to amplify three distinct amplicons to cover the entire RSV genome. The protocol described here can be successfully replicated in several instances (approximately 95%) in samples with a relatively low viral load, typically corresponding to cycle of quantification values of 27-32. The amplicon-based protocol produced meaningful sequencing results in terms of median depth of coverage (more than 12000×) and median of mapped reads (> 1 × 10

Indexed as

Genome, ViralHigh-Throughput Nucleotide SequencingRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsWhole Genome SequencingHumansInfantViral Loadamplicon‐based protocolmolecular epidemiologynext‐generation sequencingrespiratory syncytial viruswhole‐genome sequencing

Identifiers

PMID40832913
PMCPMC12365941

What OpenQuestion holds

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LicenceCC BY
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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.