Evidence map›Paper›PMID 27042253›Full record

ArticleThe annals of applied statistics2016

Reconstructing transmission trees for communicable diseases using densely sampled genetic data.

Colin J Worby, Philip D O'Neill, Theodore Kypraios, Julie V Robotham, Daniela De Angelis, Edward J P Cartwright, Sharon J Peacock, Ben S Cooper

Abstract read
In one paragraph

Article in The annals of applied statistics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Investigating pathways of vancomycin-resistantmedRxiv : the preprint server for health sciences · 2026
    Article
  2. Article
  3. Article
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  7. Molecular source attribution.PLoS computational biology · 2022
    Article
  8. Article
  9. Reconstruction of the Transmission Chain of COVID-19 Outbreak in Beijing's Xinfadi Market, China.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2022
    Article
  10. Review
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  19. Analysing livestock network data for infectious disease control: an argument for routine data collection in emerging economies.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Article
  20. 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

8 authors.

Colin J WorbySchool of Mathematical Sciences, University of Nottingham, Nottingham, UK; Center for Communicable Disease Dynamics, Harvard TH Chan School of Public Health, Boston, USA.
Philip D O'NeillSchool of Mathematical Sciences, University of Nottingham, Nottingham, UK.
Theodore KypraiosSchool of Mathematical Sciences, University of Nottingham, Nottingham, UK.
Julie V RobothamModelling & Economics Unit, Public Health England, London, UK.
Daniela De AngelisMRC Biostatistics Unit, University of Cambridge, Cambridge, UK.
Edward J P CartwrightDepartment of Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK.
Sharon J PeacockDepartment of Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, UK.
Ben S CooperCentre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK; Mahidol-Oxford Tropical Medicine Research Unit, Bangkok, Thailand.

Funding

Understanding and controlling antibiotic resistanceU54GM088558 · NIGMS · HARVARD SCHOOL OF PUBLIC HEALTH · PI HANAGE, WILLIAM · 2009 to 2018
$26.4M
Medical Research Council G1000803Medical Research Council MC_U105260556Medical Research Council MR/K006924/1NIGMS NIH HHS U54 GM088558Wellcome Trust
6 · The paper itself

Abstract

Whole genome sequencing of pathogens from multiple hosts in an epidemic offers the potential to investigate who infected whom with unparalleled resolution, potentially yielding important insights into disease dynamics and the impact of control measures. We considered disease outbreaks in a setting with dense genomic sampling, and formulated stochastic epidemic models to investigate person-to-person transmission, based on observed genomic and epidemiological data. We constructed models in which the genetic distance between sampled genotypes depends on the epidemiological relationship between the hosts. A data augmented Markov chain Monte Carlo algorithm was used to sample over the transmission trees, providing a posterior probability for any given transmission route. We investigated the predictive performance of our methodology using simulated data, demonstrating high sensitivity and specificity, particularly for rapidly mutating pathogens with low transmissibility. We then analyzed data collected during an outbreak of methicillin-resistant

Identifiers

PMID27042253
PMCPMC4817375

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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.