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Personal regulome navigation of cancer

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A systematic approach to understanding the noncoding genome in cancer promises to improve cancer diagnosis and therapy. Tracking the landscape of gene control in individual patients and single cells yields many insights for inherited and somatic mutations in cancer, extrachromosomal oncogene amplifications and cancer immunotherapy. New technologies and bold therapeutic approaches are paving the way to truly envisage personalized cancer medicine in the future.

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Fig. 1: Layering insights from regulomes.

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Acknowledgements

Supported by NIH RM1-HG007735, R35-CA209919. H.Y.C. is an Investigator of the Howard Hughes Medical Institute.

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Correspondence to Howard Y. Chang.

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Competing interests

H.Y.C. is a co-founder of Accent Therapeutics, Boundless Bio, and is an advisor of 10x Genomics, Arsenal Biosciences and Spring Discovery.

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Chang, H.Y. Personal regulome navigation of cancer. Nat Rev Cancer 21, 609–610 (2021). https://doi.org/10.1038/s41568-021-00381-x

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