Evidence map›Paper›PMID 41493011›Full record

ArticleMolecular biology and evolution2026

Phylodynamics of Somatic Evolution: A Likelihood-Based Approach for Cellular Reproduction.

Tobias Dieselhorst, Johannes Berg

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

2 authors.

Tobias DieselhorstInstitute for Biological Physics, University of Cologne, Zülpicher Str. 77, Cologne 50937, Germany.ORCID 0000-0001-5182-3697
Johannes BergInstitute for Biological Physics, University of Cologne, Zülpicher Str. 77, Cologne 50937, Germany.ORCID 0000-0001-6569-3061

Funding

Deutsche Forschungsgemeinschaft SFB1310/2 - 325931972
6 · The paper itself

Abstract

Understanding the evolutionary dynamics of cell populations requires models that link observed phylogenetic patterns to the underlying processes of cell division, death, and mutation. Classical phylodynamic inference methods-developed primarily for macroevolutionary settings-assume that mutations accrue in calendar time and often rely on a molecular clock. Here, we introduce a framework that ties mutations to discrete birth (division) events. In this setting, mutations accumulate via a compound Poisson process, capturing both visible and hidden cell divisions within the reconstructed phylogenetic tree. We present a computationally efficient dynamic programming algorithm to compute the likelihood based on tree topologies with associated mutations, integrating over latent variables such as branch durations and unobserved cell divisions. Our method is applicable to large-scale single-cell datasets, and we demonstrate its utility on simulated data and on single-cell phylogenies of hematopoietic stem cells.

Indexed as

Biological EvolutionModels, GeneticPhylogenyAlgorithmsCell DivisionEvolution, MolecularHumansLikelihood FunctionsMutationSingle-Cell Analysisphylodynamics inferencesingle-cell phylogenetics

Identifiers

PMID41493011
PMCPMC12877876

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.