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Identifying this tipping point and its driving network is essential to avert or delay disastrous outcomes. However, most traditional approaches built upon undirected networks still suffer from a lack of robustness and effectiveness when implemented based on high-dimensional small-sample data, especially for single-cell data. To address this challenge, we develop a directed network flow entropy (DNFE) method, which can transform measured omics data into a directed network. This method is applicable to both single-cell RNA-sequencing (scRNA-seq) and bulk data. Applying this algorithm to six real datasets, including three single-cell datasets, two bulk tumor datasets, and a blood dataset, the method is proved to be effective not only in identifying critical states, as well as their dynamic network biomarkers, but also in helping explore regulatory relationships between genes. Numerical simulation results demonstrate that the DNFE algorithm is robust across various noise levels and outperforms existing methods in detecting tipping points. Furthermore, the numerical simulations for 100-node and 1000-node gene regulatory networks illustrate the method\u2019s application for large-scale data. The DNFE method predicts active transcription factors, and further identified \u201cdark genes\u201d, which are usually overlooked with traditional methods.<\/jats:p>","DOI":"10.1371\/journal.pcbi.1013336","type":"journal-article","created":{"date-parts":[[2025,7,29]],"date-time":"2025-07-29T17:40:16Z","timestamp":1753810816000},"page":"e1013336","update-policy":"https:\/\/doi.org\/10.1371\/journal.pcbi.corrections_policy","source":"Crossref","is-referenced-by-count":5,"title":["DNFE: Directed network flow entropy for detecting tipping points during biological 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