Evidence map›Paper›PMID 28545083›Full record

ArticlePLoS computational biology2017

Simultaneous inference of phylogenetic and transmission trees in infectious disease outbreaks.

Don Klinkenberg, Jantien A Backer, Xavier Didelot, Caroline Colijn, Jacco Wallinga

Abstract read
In one paragraph

Article in PLoS computational biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing 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

81 citing papers in PubMed.

  1. Article
  2. Quantifying the community transmission ofEmerging microbes & infections · 2026
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21 more citing papers are in PubMed but not listed here.

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.

Don KlinkenbergDepartment of Epidemiology and Surveillance, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.ORCID 0000-0002-9449-6873
Jantien A BackerDepartment of Epidemiology and Surveillance, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.ORCID 0000-0003-4169-5665
Xavier DidelotDepartment of Infectious Disease Epidemiology, Imperial College London, London, United Kingdom.ORCID 0000-0003-1885-500X
Caroline ColijnDepartment of Mathematics, Imperial College London, London, United Kingdom.ORCID 0000-0001-6097-6708
Jacco WallingaDepartment of Epidemiology and Surveillance, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.ORCID 0000-0003-1725-5627

Funding

Medical Research Council MR/ N010760/1Medical Research Council MR/N010760/1
6 · The paper itself

Abstract

Whole-genome sequencing of pathogens from host samples becomes more and more routine during infectious disease outbreaks. These data provide information on possible transmission events which can be used for further epidemiologic analyses, such as identification of risk factors for infectivity and transmission. However, the relationship between transmission events and sequence data is obscured by uncertainty arising from four largely unobserved processes: transmission, case observation, within-host pathogen dynamics and mutation. To properly resolve transmission events, these processes need to be taken into account. Recent years have seen much progress in theory and method development, but existing applications make simplifying assumptions that often break up the dependency between the four processes, or are tailored to specific datasets with matching model assumptions and code. To obtain a method with wider applicability, we have developed a novel approach to reconstruct transmission trees with sequence data. Our approach combines elementary models for transmission, case observation, within-host pathogen dynamics, and mutation, under the assumption that the outbreak is over and all cases have been observed. We use Bayesian inference with MCMC for which we have designed novel proposal steps to efficiently traverse the posterior distribution, taking account of all unobserved processes at once. This allows for efficient sampling of transmission trees from the posterior distribution, and robust estimation of consensus transmission trees. We implemented the proposed method in a new R package phybreak. The method performs well in tests of both new and published simulated data. We apply the model to five datasets on densely sampled infectious disease outbreaks, covering a wide range of epidemiological settings. Using only sampling times and sequences as data, our analyses confirmed the original results or improved on them: the more realistic infection times place more confidence in the inferred transmission trees.

Indexed as

Bacterial InfectionsDisease Transmission, InfectiousPhylogenyVirus DiseasesAlgorithmsBacteriaComputational BiologyGenome, BacterialGenome, ViralHumansPolymorphism, Single NucleotideViruses

Identifiers

PMID28545083
PMCPMC5436636

What OpenQuestion holds

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LicenceCC BY
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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.