CeiTEA: Adaptive Hierarchy of Single Cells with Topological Entropy

Bowen Tan (Co-first Author), Shiying Li (Co-first Author), Mengbo Wang, Shuai Cheng Li*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

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Abstract

Advances in single-cell RNA sequencing (scRNA-seq) enable detailed analysis of cellular heterogeneity, but existing clustering methods often fail to capture the complex hierarchical structures of cell types and subtypes. CeiTEA is introduced, a novel algorithm for adaptive hierarchical clustering based on topological entropy (TE), designed to address this challenge. CeiTEA constructs a multi-nary partition tree that optimally represents relationships and diversity among cell types by minimizing TE. This method combines a bottom-up strategy for hierarchy construction with a top-down strategy for local diversification, facilitating the identification of smaller hierarchical structures within subtrees. CeiTEA is evaluated on both simulated and real-world scRNA-seq datasets, demonstrating superior clustering performance compared to state-of-the-art tools like Louvain, Leiden, K-means, and SEAT. In simulated multi-layer datasets, CeiTEA demonstrated superior performance in retrieving hierarchies with a lower average clustering information distance of 0.15, compared to 0.39 from SEAT and 0.67 from traditional hierarchical clustering methods. On real datasets, the CeiTEA hierarchy reflects the developmental potency of various cell populations, validated by gene ontology enrichment, cell-cell interaction, and pseudo-time analysis. These findings highlight CeiTEA's potential as a powerful tool for understanding complex relationships in single-cell data, with applications in tumor heterogeneity and tissue specification.  © 2025 The Author(s). Advanced Science published by Wiley-VCH GmbH
Original languageEnglish
Article number2503539
JournalAdvanced Science
Volume12
Issue number6
Online published17 Apr 2025
DOIs
Publication statusPublished - Jul 2025

Funding

The authors would like to express our gratitude to Dr. Lingxi Chen for generously providing the preprocessed affinity/similarity matrices of nine scRNA-seq datasets. The authors are also grateful to Ms. Yingying Yu for her insightful suggestions on trajectory and pseudo-time analysis. The authors acknowledge the valuable suggestions received from various individuals. This project was supported by the General Research Fund provided by the Research Grants Council of the HKSAR (Project No. 9043559; CityU 11218823), and the National Natural Science Fundation of China (32270687).

Research Keywords

  • entropy
  • hierarchical clustering
  • single cell

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

RGC Funding Information

  • RGC-funded

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