Evidence map›Paper›PMID 28263987›Full record

ArticlePLoS computational biology2017

Inferring epidemiological parameters from phylogenies using regression-ABC: A comparative study.

Emma Saulnier, Olivier Gascuel, Samuel Alizon

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 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Phylogenetic Methods Meet Deep Learning.Genome biology and evolution · 2025
    Article
  5. phyddle: software for exploring phylogenetic models with deep learning.bioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Statistical Challenges in Tracking the Evolution of SARS-CoV-2.Statistical science : a review journal of the Institute of Mathematical Statistics · 2022
    Article
  11. Evolution during primary HIV infection does not require adaptive immune selection.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
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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

3 authors.

Emma SaulnierLaboratoire Maladies Infectieuses et Vecteurs: Ecologie, Génétique, Evolution et Contrôle - UMR CNRS 5290, IRD 224 et UM, Montpellier, France.ORCID 0000-0002-8392-0624
Olivier GascuelInstitut de Biologie Computationnelle (IBC) and Laboratoire d'Informatique, de Robotique et de Microélectronique de Montpellier (LIRMM) - UMR 5506, CNRS et UM, Montpellier, France.
Samuel AlizonLaboratoire Maladies Infectieuses et Vecteurs: Ecologie, Génétique, Evolution et Contrôle - UMR CNRS 5290, IRD 224 et UM, Montpellier, France.ORCID 0000-0002-0779-9543

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inferring epidemiological parameters such as the R0 from time-scaled phylogenies is a timely challenge. Most current approaches rely on likelihood functions, which raise specific issues that range from computing these functions to finding their maxima numerically. Here, we present a new regression-based Approximate Bayesian Computation (ABC) approach, which we base on a large variety of summary statistics intended to capture the information contained in the phylogeny and its corresponding lineage-through-time plot. The regression step involves the Least Absolute Shrinkage and Selection Operator (LASSO) method, which is a robust machine learning technique. It allows us to readily deal with the large number of summary statistics, while avoiding resorting to Markov Chain Monte Carlo (MCMC) techniques. To compare our approach to existing ones, we simulated target trees under a variety of epidemiological models and settings, and inferred parameters of interest using the same priors. We found that, for large phylogenies, the accuracy of our regression-ABC is comparable to that of likelihood-based approaches involving birth-death processes implemented in BEAST2. Our approach even outperformed these when inferring the host population size with a Susceptible-Infected-Removed epidemiological model. It also clearly outperformed a recent kernel-ABC approach when assuming a Susceptible-Infected epidemiological model with two host types. Lastly, by re-analyzing data from the early stages of the recent Ebola epidemic in Sierra Leone, we showed that regression-ABC provides more realistic estimates for the duration parameters (latency and infectiousness) than the likelihood-based method. Overall, ABC based on a large variety of summary statistics and a regression method able to perform variable selection and avoid overfitting is a promising approach to analyze large phylogenies.

Indexed as

Bayes TheoremModels, StatisticalAlgorithmsComputer SimulationDisease OutbreaksEbolavirusHemorrhagic Fever, EbolaHumansIncidencePhylogenyRegression AnalysisRisk FactorsSierra LeoneVirus Latency

Identifiers

PMID28263987
PMCPMC5358897

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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.