ArticleMolecular biology and evolution2025
Bayesian Phylodynamic Inference of Multitype Population Trajectories Using Genomic Data.
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 6 papers.
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.
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.
Who cites it
6 citing papers in PubMed.
- Rapid Phylogeographic Inference of Regional Epidemic Dynamics for Routine Genomic Surveillance.Research square · 2026Article
- Assessing the inference of single-cell phylogenies and population dynamics from CRISPR lineage recordings.PLoS computational biology · 2026Article
- SAASI: Sampling Aware Ancestral State Inference.Nature communications · 2026Article
- Age-dependent Phylodynamics with Application to Single-cell Lineage Trees.Molecular biology and evolution · 2026Article
- Introduction and inter-species transmission dynamics of high pathogenicity avian influenza H5N1 viruses in Japan 2021-25.Virus evolution · 2026Article
- Poultry farm density and proximity drive highly pathogenic avian influenza spread.Communications biology · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Phylodynamic methods provide a coherent framework for the inference of population parameters directly from genetic data. They are an important tool for understanding both the spread of epidemics as well as long-term macroevolutionary trends in speciation and extinction. In particular, phylodynamic methods based on multitype birth-death models have been used to infer the evolution of discrete traits, the movement of individuals or pathogens between geographic locations or host types, and the transition of infected individuals between disease stages. In these models, population heterogeneity is treated by assigning individuals to different discrete types. Typically, methods which allow inference of parameters under multitype birth-death models integrate over the possible birth-death trajectories (i.e. the type-specific population size functions) to reduce the computational demands of the inference. As a result, it has not been possible to use these methods to directly infer the dynamics of trait-specific population sizes, infected host counts or other such demographic quantities. In this article, we present a method which infers these multitype trajectories with minimal additional computational cost beyond that of existing methods. We demonstrate the practicality of our approach by applying it to a previously published set of Middle East respiratory syndrome coronavirus genomes, inferring the numbers of human and camel cases through time, together with the number and timing of spillovers from the camel reservoir. This application highlights the multitype population trajectory's ability to elucidate properties of the population which are not directly ancestral to its sampled members.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.