Machine learning to dissect perturbations in complex cellular systems

被引:0
|
作者
Monfort-Lanzas, Pablo [1 ,2 ]
Rungger, Katja [1 ]
Madersbacher, Leonie [1 ]
Hackl, Hubert [1 ]
机构
[1] Med Univ Innsbruck, Inst Bioinformat, Bioctr, Innrain 80, A-6020 Innsbruck, Austria
[2] Med Univ Innsbruck, Inst Med Biochem, Bioctr, Innsbruck, Austria
来源
COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL | 2025年 / 27卷
关键词
Artificial intelligence; Machine learning; Perturbation; Dose response; CRISPR-Cas9; screening; Single cell RNA sequencing; Spatial transcriptomics; DRUG RESPONSE; RNA-SEQ; SINGLE; GENERATION; MODEL; MECHANISMS; CIRCUITS; SCREENS; GENOME;
D O I
10.1016/j.csbj.2025.02.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Understanding the responses of biological systems to various perturbations, such as genetic, chemical, or environmental challenges, is essential for reconstructing causal network models. Emerging single-cell technologies have become instrumental in elucidating cell states and phenotypes and they have been used in combination with genetic screening. Recent advances in machine learning and artificial intelligence architectures have stimulated the development of computational tools for modeling perturbations and the response to compounds. This study outlined core principles underpinning perturbation analysis and discussed the methodologies and analytical frameworks used to decode drug and genetic perturbation responses, complex multicellular interactions, and network dynamics. The current tools used for various applications were overviewed. These developments hold great promise for improving drug development and personalized medicine. Foundation models and perturbation cell and tissue atlases offer immense potential for advancing our understanding of cellular behavior and disease mechanisms.
引用
收藏
页码:832 / 842
页数:11
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