Evidence map›Paper›PMID 40877260›Full record

ArticleNature communications2025

A graph homomorphism approach for unraveling histories of metastatic cancers and viral outbreaks under evolutionary constraints.

Kiril Kuzmin, Henri Schmidt, Maryam Kafi Kang, Sagi Snir, Benjamin J Raphael, Pavel Skums

Abstract read
In one paragraph

Article in Nature communications, 2025. 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. Review
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

6 authors.

Kiril KuzminDepartment of Computer Science, Georgia State University, Atlanta, GA, USA.
Henri SchmidtDepartment of Computer Science, Princeton University, Princeton, NJ, USA.
Maryam Kafi KangSchool of Computing, University of Connecticut, Storrs, CT, USA.
Sagi SnirDepartment of Evolutionary and Environmental Biology, University of Haifa, Haifa, Israel.
Benjamin J RaphaelDepartment of Computer Science, Princeton University, Princeton, NJ, USA.
Pavel SkumsSchool of Computing, University of Connecticut, Storrs, CT, USA. pavel.skums@uconn.edu.ORCID http://orcid.org/0000-0003-4007-5624

Funding

Comprehensive and Robust Tools for Analysis of Tumor Heterogeneity and EvolutionU24CA248453 · NCI · PRINCETON UNIVERSITY · PI Benjamin Raphael · 2020 to 2026
$4.7M
National Science Foundation (NSF) 2415562National Science Foundation (NSF) 2415564NCI NIH HHS U24 CA248453
6 · The paper itself

Abstract

Viral infections and cancers are driven by evolution of populations of highly mutable genomic variants. A key evolutionary process in these populations is their migration or spread via transmission or metastasis. Understanding this process is crucial for research, clinical practice, and public health, yet tracing spread pathways is challenging. Phylogenetics offers the main methodological framework for this problem, with challenges including determining the conditions when a phylogenetic tree reflects the underlying migration tree structure, and balancing computational efficiency, flexibility, and biological realism. We tackle these challenges using the powerful machinery of graph homomorphisms, a mathematical concept describing how one graph can be mapped onto another while preserving its structure. We focus on metastatic migrations and viral host-to-host transmissions in outbreak settings. We investigate how structural constraints on migration patterns influence the relationship between phylogenetic and migration trees and propose algorithms to evaluate trees consistency under varying conditions. Leveraging our findings, we introduce a framework for inferring transmission/migration trees by sampling potential solutions from a prior random tree distribution and identifying a subsample consistent with a given phylogeny. By varying the prior distribution, this approach generalizes several existing models, offering a versatile strategy applicable in diverse settings.

Indexed as

Disease OutbreaksNeoplasmsVirus DiseasesAlgorithmsEvolution, MolecularHumansNeoplasm MetastasisPhylogeny

Identifiers

PMID40877260
PMCPMC12394457

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.