Evidence map›Paper›PMID 41056469›Full record

ArticleMolecular biology and evolution2025

Navigating Sampling Bias in Discrete Phylogeographic Analysis: Assessing the Performance of an Adjusted Bayes Factor.

Fabiana Gámbaro, Maylis Layan, Guy Baele, Bram Vrancken, Simon Dellicour

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

5 authors.

Fabiana GámbaroSpatial Epidemiology Lab (SpELL), Université Libre de Bruxelles, 50 av. F.D Roosevelt, 1050 Brussels, Belgium.ORCID 0000-0001-7760-2112
Maylis LayanMathematical Modelling of Infectious Diseases Unit, Institut Pasteur, Université Paris, UMR2000, CNRS, 25-28 rue du Docteur Roux, 75015 Paris, France.ORCID 0000-0003-3092-686X
Guy BaeleDepartment of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Herestraat 49 - Box 1030, 3000 Leuven, Belgium.ORCID 0000-0002-1915-7732
Bram VranckenSpatial Epidemiology Lab (SpELL), Université Libre de Bruxelles, 50 av. F.D Roosevelt, 1050 Brussels, Belgium.ORCID 0000-0001-6547-5283
Simon DellicourSpatial Epidemiology Lab (SpELL), Université Libre de Bruxelles, 50 av. F.D Roosevelt, 1050 Brussels, Belgium.ORCID 0000-0001-9558-1052

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bayesian phylogeographic inference is widely used in molecular epidemiological studies to reconstruct the dispersal history of pathogens. Discrete phylogeographic analysis treats geographic locations as discrete traits and infers lineage transition events among them, and is typically followed by a Bayes factor (BF) test to assess the statistical support. In the standard BF (BFstd) test, the relative abundance of the involved trait states is not considered, which can be problematic in the case of unbalanced sampling. Existing methods to correct sampling bias in discrete phylogeographic analyses using continuous-time Markov chain (CTMC) model, often require additional epidemiological information to balance the sampling effort among locations. As such data is not necessarily available, alternative approaches that rely solely on available genomic data are needed. In this perspective, we assess the performance of a modification of the BFstd, the adjusted Bayes factor (BFadj), which incorporates information on the relative abundance of samples by location when inferring support for transition events and root location inference without requiring additional data. Using a simulation framework, we assess the statistical performance of BFstd and BFadj under varying levels of sampling bias, estimating their type I and type II error rates. Our results show that BFadj complements the BFstd by reducing type I errors at the cost increasing type II errors for inferred transition events, while improving type I and type II errors in root location inference. Our findings provide guidelines for implementing the complementary BFadj to detect and mitigate sampling bias in discrete phylogeographic inference using CTMC modeling.

Indexed as

PhylogeographySelection BiasBayes TheoremComputer SimulationMarkov ChainsModels, GeneticBayes factordiscrete phylogeographymolecular epidemiologyviruses

Identifiers

PMID41056469
PMCPMC12571152

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.