Journal
NATURE COMMUNICATIONS
Volume 11, Issue 1, Pages -Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-020-16539-4
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Funding
- NIH/NIGMS [R01GM125632]
- NIH/NHLBI [R01HL133254, R01HL148338]
- US Department of Defense [W81XWH-15-1-0639, W81XWH-17-1-0357]
- American Cancer Society [TBE-128382]
- NIH/NCI [R01CA208257]
- NIH/NCI (Prostate SPORE) [P50CA180995 DRP]
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Conversion between cell types, e.g., by induced expression of master transcription factors, holds great promise for cellular therapy. Our ability to manipulate cell identity is constrained by incomplete information on cell identity genes (CIGs) and their expression regulation. Here, we develop CEFCIG, an artificial intelligent framework to uncover CIGs and further define their master regulators. On the basis of machine learning, CEFCIG reveals unique histone codes for transcriptional regulation of reported CIGs, and utilizes these codes to predict CIGs and their master regulators with high accuracy. Applying CEFCIG to 1,005 epigenetic profiles, our analysis uncovers the landscape of regulation network for identity genes in individual cell or tissue types. Together, this work provides insights into cell identity regulation, and delivers a powerful technique to facilitate regenerative medicine.
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