TY - JOUR
T1 - The trifecta of single-cell, systems-biology, and machine-learning approaches
AU - Weiskittel, Taylor M.
AU - Correia, Cristina
AU - Yu, Grace T.
AU - Ung, Choong Yong
AU - Kaufmann, Scott H.
AU - Billadeau, Daniel D.
AU - Li, Hu
N1 - Funding Information:
Funding: This work was supported by grants from the National Institutes of Health (NIH) [R01CA208 517, R01AG056318, R01AG61796, P50CA136393], the Mayo Clinic Center for Biomedical Discovery, the Mayo Clinic Center for Individualized Medicine, the Mayo Clinic Cancer Center, and the David F. and Margaret T. Grohne Cancer Immunology and Immunotherapy Program.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/7
Y1 - 2021/7
N2 - Together, single-cell technologies and systems biology have been used to investigate previously unanswerable questions in biomedicine with unparalleled detail. Despite these advances, gaps in analytical capacity remain. Machine learning, which has revolutionized biomedical imaging analysis, drug discovery, and systems biology, is an ideal strategy to fill these gaps in single-cell studies. Machine learning additionally has proven to be remarkably synergistic with single-cell data because it remedies unique challenges while capitalizing on the positive aspects of single-cell data. In this review, we describe how systems-biology algorithms have layered machine learning with biological components to provide systems level analyses of single-cell omics data, thus elucidating complex biological mechanisms. Accordingly, we highlight the trifecta of single-cell, systems-biology, and machine-learning approaches and illustrate how this trifecta can significantly contribute to five key areas of scientific research: cell trajectory and identity, individualized medicine, pharmacology, spatial omics, and multi-omics. Given its success to date, the systems-biology, single-cell omics, and machine-learning trifecta has proven to be a potent combination that will further advance biomedical research.
AB - Together, single-cell technologies and systems biology have been used to investigate previously unanswerable questions in biomedicine with unparalleled detail. Despite these advances, gaps in analytical capacity remain. Machine learning, which has revolutionized biomedical imaging analysis, drug discovery, and systems biology, is an ideal strategy to fill these gaps in single-cell studies. Machine learning additionally has proven to be remarkably synergistic with single-cell data because it remedies unique challenges while capitalizing on the positive aspects of single-cell data. In this review, we describe how systems-biology algorithms have layered machine learning with biological components to provide systems level analyses of single-cell omics data, thus elucidating complex biological mechanisms. Accordingly, we highlight the trifecta of single-cell, systems-biology, and machine-learning approaches and illustrate how this trifecta can significantly contribute to five key areas of scientific research: cell trajectory and identity, individualized medicine, pharmacology, spatial omics, and multi-omics. Given its success to date, the systems-biology, single-cell omics, and machine-learning trifecta has proven to be a potent combination that will further advance biomedical research.
KW - Machine learning
KW - Single-cell omics
KW - Single-cell systems biology
KW - Systems biology
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U2 - 10.3390/genes12071098
DO - 10.3390/genes12071098
M3 - Review article
C2 - 34356114
AN - SCOPUS:85111425252
SN - 2073-4425
VL - 12
JO - Genes
JF - Genes
IS - 7
M1 - 1098
ER -