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NetAct: a computational platform to construct core transcription factor regulatory networks using gene activity

A major question in systems biology is how to identify the core gene regulatory circuit that governs the decision-making of a biological process. Here, we develop a computational platform, named NetAct, for constructing core transcription factor regulatory networks using both transcriptomics data an...

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Detalles Bibliográficos
Autores principales: Su, Kenong, Katebi, Ataur, Kohar, Vivek, Clauss, Benjamin, Gordin, Danya, Qin, Zhaohui S., Karuturi, R. Krishna M., Li, Sheng, Lu, Mingyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9793520/
https://www.ncbi.nlm.nih.gov/pubmed/36575445
http://dx.doi.org/10.1186/s13059-022-02835-3
Descripción
Sumario:A major question in systems biology is how to identify the core gene regulatory circuit that governs the decision-making of a biological process. Here, we develop a computational platform, named NetAct, for constructing core transcription factor regulatory networks using both transcriptomics data and literature-based transcription factor-target databases. NetAct robustly infers regulators’ activity using target expression, constructs networks based on transcriptional activity, and integrates mathematical modeling for validation. Our in silico benchmark test shows that NetAct outperforms existing algorithms in inferring transcriptional activity and gene networks. We illustrate the application of NetAct to model networks driving TGF-β-induced epithelial-mesenchymal transition and macrophage polarization. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-022-02835-3.