Identification of Critical States in Complex Biological Systems Using Cell-Specific Causal Network Entropy

Abrupt shifts, referred to as critical transitions, are frequently observed in complex biological systems, characterized by marked qualitative changes occurring from one stable state to another through a pre-transitional/critical state. Pinpointing such critical states, along with the signaling molecules, can provide valuable insights into the fundamental mechanisms of intricate biological processes. However, the identification and early warning of the critical state remains a challenge, particularly in model-free cases with high-dimensional single-cell data, where traditional statistical methods often prove inadequate due to the inherent sparsity, noise, and heterogeneity of the data. In this study, we propose a novel quantitative method, cell-specific causal network entropy (CCNE), to infer the specific causal network for each cell and quantify dynamic causal changes, thereby enabling the identification of critical states in complex biological processes at the single-cell level. We validated the accuracy and effectiveness of the proposed approach through numerical simulations and 5 distinct real-world single-cell datasets. Compared to existing methods for detecting critical states, the proposed CCNE exhibits enhanced effectiveness in identifying critical transition signals. Moreover, CCNE score is a computational tool for distinguishing temporal changes in cellular heterogeneity and demonstrates satisfactory performance in clustering cells over time. In addition, the reliability of CCNE is further emphasized through the functional enrichment and pathway analysis of signaling molecules.

Authors

Institutions

Publication Details

Journal
Research
Published
2025-01-01
DOI
https://doi.org/10.34133/research.0852
Citations
1
Primary Topic
Gene Regulatory Network Analysis
Type
article
Field-Weighted Citation Impact
0.81

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Identification of Critical States in Complex Biological Systems Using Cell-Specific Causal Network Entropy

Fei Ling, Jiayuan Zhong, Rui Liu, Ziyi Huang et al.
1 citations
Research
Gene Regulatory Network Analysis
0.81
article

Identification of Critical States in Complex Biological Systems Using Cell-Specific Causal Network Entropy

Fei Ling, Jiayuan Zhong, Rui Liu, Ziyi Huang, Pei Chen, J. F. Qiu
article en
1 citations

Abstract

Abrupt shifts, referred to as critical transitions, are frequently observed in complex biological systems, characterized by marked qualitative changes occurring from one stable state to another through a pre-transitional/critical state. Pinpointing such critical states, along with the signaling molecules, can provide valuable insights into the fundamental mechanisms of intricate biological processes. However, the identification and early warning of the critical state remains a challenge, particularly in model-free cases with high-dimensional single-cell data, where traditional statistical methods often prove inadequate due to the inherent sparsity, noise, and heterogeneity of the data. In this study, we propose a novel quantitative method, cell-specific causal network entropy (CCNE), to infer the specific causal network for each cell and quantify dynamic causal changes, thereby enabling the identification of critical states in complex biological processes at the single-cell level. We validated the accuracy and effectiveness of the proposed approach through numerical simulations and 5 distinct real-world single-cell datasets. Compared to existing methods for detecting critical states, the proposed CCNE exhibits enhanced effectiveness in identifying critical transition signals. Moreover, CCNE score is a computational tool for distinguishing temporal changes in cellular heterogeneity and demonstrates satisfactory performance in clustering cells over time. In addition, the reliability of CCNE is further emphasized through the functional enrichment and pathway analysis of signaling molecules.

ResearchVol. 8
Foshan University (CN), South China University of Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 25%
Gene Regulatory Network Analysis
0.81
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.