4.7 Article

Machine learning for perturbational single-cell omics

期刊

CELL SYSTEMS
卷 12, 期 6, 页码 522-537

出版社

CELL PRESS
DOI: 10.1016/j.cels.2021.05.016

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资金

  1. Chan Zuckerberg Initiative DAF
  2. Silicon Valley Community Foundation [2019-002438]
  3. BMBF [01IS18053A, 01IS18036B]
  4. Helmholtz Association's Initiative and Networking Fund through Helmholtz AI [ZT-I-PF-5-01]
  5. Helmholtz Association's Initiative and Networking Fund through sparse2big [ZT-I-007]

向作者/读者索取更多资源

Cell biology faces limitations in collecting complete data on cellular phenotypes and responses to perturbation, but recent advances in machine learning and deep learning are starting to address this issue, particularly in the field of single-cell data.
Cell biology is fundamentally limited in its ability to collect complete data on cellular phenotypes and the wide range of responses to perturbation. Areas such as computer vision and speech recognition have addressed this problem of characterizing unseen or unlabeled conditions with the combined advances of big data, deep learning, and computing resources in the past 5 years. Similarly, recent advances in machine learning approaches enabled by single-cell data start to address prediction tasks in perturbation response modeling. We first define objectives in learning perturbation response in single-cell omics; survey existing approaches, resources, and datasets (https://github.com/theislab/sc-pert); and discuss how a perturbation atlas can enable deep learning models to construct an informative perturbation latent space. We then examine future avenues toward more powerful and explainable modeling using deep neural networks, which enable the integration of disparate information sources and an understanding of heterogeneous, complex, and unseen systems.

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