Evidence map›Paper›PMID 37703335›Full record

ArticleSystematic biology2023

Fast and Accurate Maximum-Likelihood Estimation of Multi-Type Birth-Death Epidemiological Models from Phylogenetic Trees.

Anna Zhukova, Frédéric Hecht, Yvon Maday, Olivier Gascuel

Open access · hybridAbstract read
In one paragraph

Article in Systematic biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
4.1field-weighted citation impact, top 6% of its field
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

8 citing papers in PubMed, 13 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Anna ZhukovaUnité Bioinformatique Evolutive, Institut Pasteur, Université de Paris, 28 rue du docteur Roux, 75015 Paris, France.ORCID 0000-0003-2200-7935
Frédéric HechtSorbonne Université, CNRS, Université Paris Cité, Laboratoire Jacques-Louis Lions (LJLL), 4 place Jussieu, F-75005 Paris, France.
Yvon MadaySorbonne Université, CNRS, Université Paris Cité, Laboratoire Jacques-Louis Lions (LJLL), 4 place Jussieu, F-75005 Paris, France.
Olivier GascuelUnité Bioinformatique Evolutive, Institut Pasteur, Université de Paris, 28 rue du docteur Roux, 75015 Paris, France.ORCID 0000-0002-9412-9723
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FR

Funding

European Research Council 810367
6 · The paper itself

Abstract

Multi-type birth-death (MTBD) models are phylodynamic analogies of compartmental models in classical epidemiology. They serve to infer such epidemiological parameters as the average number of secondary infections Re and the infectious time from a phylogenetic tree (a genealogy of pathogen sequences). The representatives of this model family focus on various aspects of pathogen epidemics. For instance, the birth-death exposed-infectious (BDEI) model describes the transmission of pathogens featuring an incubation period (when there is a delay between the moment of infection and becoming infectious, as for Ebola and SARS-CoV-2), and permits its estimation along with other parameters. With constantly growing sequencing data, MTBD models should be extremely useful for unravelling information on pathogen epidemics. However, existing implementations of these models in a phylodynamic framework have not yet caught up with the sequencing speed. Computing time and numerical instability issues limit their applicability to medium data sets (≤ 500 samples), while the accuracy of estimations should increase with more data. We propose a new highly parallelizable formulation of ordinary differential equations for MTBD models. We also extend them to forests to represent situations when a (sub-)epidemic started from several cases (e.g., multiple introductions to a country). We implemented it for the BDEI model in a maximum likelihood framework using a combination of numerical analysis methods for efficient equation resolution. Our implementation estimates epidemiological parameter values and their confidence intervals in two minutes on a phylogenetic tree of 10,000 samples. Comparison to the existing implementations on simulated data shows that it is not only much faster but also more accurate. An application of our tool to the 2014 Ebola epidemic in Sierra-Leone is also convincing, with very fast calculation and precise estimates. As MTBD models are closely related to Cladogenetic State Speciation and Extinction (ClaSSE)-like models, our findings could also be easily transferred to the macroevolution domain.

Indexed as

EpidemicsHemorrhagic Fever, EbolaEpidemiological ModelsHumansLikelihood FunctionsPhylogenyBirth–death modelEbolaepidemiologymathematical modellingordinary differential equationsphylodynamics

Identifiers

PMID37703335
PMCPMC10924745
OpenAlexW4386725648

What OpenQuestion holds

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LicenceCC BY-NC
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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.