Evidence map›Paper›PMID 40662787›Full record

ArticleBioinformatics (Oxford, England)2025

Bayesian inference of fitness landscapes via tree-structured branching processes.

Xiang Ge Luo, Jack Kuipers, Kevin Rupp, Koichi Takahashi, Niko Beerenwinkel

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Xiang Ge LuoDepartment of Biosystems Science and Engineering, ETH Zurich, Basel 4056, Switzerland.
Jack KuipersDepartment of Biosystems Science and Engineering, ETH Zurich, Basel 4056, Switzerland.
Kevin RuppDepartment of Biosystems Science and Engineering, ETH Zurich, Basel 4056, Switzerland.
Koichi TakahashiDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, United States.ORCID 0000-0002-8027-9659
Niko BeerenwinkelDepartment of Biosystems Science and Engineering, ETH Zurich, Basel 4056, Switzerland.ORCID 0000-0002-0573-6119

Funding

ETH ZurichEuropean Union's Horizon 2020 Research and Innovation Program 951970
6 · The paper itself

Abstract

motivationThe complex dynamics of cancer evolution, driven by mutation and selection, underlies the molecular heterogeneity observed in tumors. The evolutionary histories of tumors of different patients can be encoded as mutation trees and reconstructed in high resolution from single-cell sequencing data, offering crucial insights for studying fitness effects of and epistasis among mutations. Existing models, however, either fail to separate mutation and selection or neglect the evolutionary histories encoded by the tumor phylogenetic trees.

resultsWe introduce FiTree, a tree-structured multi-type branching process model with epistatic fitness parameterization and a Bayesian inference scheme to learn fitness landscapes from single-cell tumor mutation trees. Through simulations, we demonstrate that FiTree outperforms state-of-the-art methods in inferring the fitness landscape underlying tumor evolution. Applying FiTree to a single-cell acute myeloid leukemia dataset, we identify epistatic fitness effects consistent with known biological findings and quantify uncertainty in predicting future mutational events. The new model unifies probabilistic graphical models of cancer progression with population genetics, offering a principled framework for understanding tumor evolution and informing therapeutic strategies. AVAILABILITY AND IMPLEMENTATION: The Python package FiTree and the analysis workflows are available at https://github.com/cbg-ethz/FiTree.

Indexed as

Genetic FitnessModels, GeneticAlgorithmsBayes TheoremEpistasis, GeneticEvolution, MolecularHumansLeukemia, Myeloid, AcuteMutationNeoplasmsSingle-Cell Analysis

Identifiers

PMID40662787
PMCPMC12261431

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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.