Evidence map›Paper›PMID 41089325›Full record

ArticleVirus evolution2025

ViralBottleneck: an R package for estimating viral transmission bottlenecks from deep sequencing data using multiple methods.

Bowen Zheng, Paul C D Johnson, Joseph Hughes

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Article in Virus evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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0cells of the map it votes in
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

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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

5 · Who and what money

Authors and funding

3 authors.

Bowen ZhengMRC-University of Glasgow Centre for Virus Research, Sir Michael Stoker Building, 464 Bearsden Road, Glasgow G61 1QH, United Kingdom.
Paul C D JohnsonSchool of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Graham Kerr Building, Glasgow G12 8QQ, United Kingdom.ORCID https://orcid.org/0000-0001-6663-7520
Joseph HughesMRC-University of Glasgow Centre for Virus Research, Sir Michael Stoker Building, 464 Bearsden Road, Glasgow G61 1QH, United Kingdom.ORCID https://orcid.org/0000-0003-2556-2563

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute viral infections pose significant public health challenges. Since viral evolution, immune escape, and infection severity are influenced by how viruses spread between hosts, understanding transmission bottlenecks is crucial for predicting disease dynamics and developing effective control strategies. Transmission bottlenecks reduce viral population size and genetic diversity as the virus spreads to new hosts. Bottleneck size, defined as the number of viral individuals successfully establishing infection in a new host, varies across transmission events and can influence disease emergence and virus evolution. In this study, we introduce ViralBottleneck, an R package integrating six established methods for estimating transmission bottleneck size: the presence-absence method, Kullback-Leibler (KL) method, binomial method, two versions of the beta-binomial method, and the Wright-Fisher method. We demonstrate the package's functionality using simulated datasets generated with SANTA-Sim under different scenarios with known bottleneck sizes. Our results reveal considerable variation in estimates across methods, highlighting the impact of methodological choice on bottleneck size estimation. The code and associated tutorial are available at https://github.com/BowenArchaman/ViralBottleneck.

Indexed as

bottleneckdeep sequencingintra-host viral diversityR packagetransmission

Identifiers

PMID41089325
PMCPMC12516950

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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.