Author
Listed:
- Jiong Chen
(University of Pennsylvania School of Engineering and Applied Science
University of Pennsylvania Perelman School of Medicine)
- Matei Ionita
(University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine)
- Yanbo Feng
(University of Pennsylvania Perelman School of Medicine)
- Yinfeng Lu
(University of Pennsylvania Perelman School of Medicine
University of Pennsylvania School of Arts and Sciences)
- Patryk Orzechowski
(University of Pennsylvania Perelman School of Medicine
AGH University of Science and Technology)
- Sumita Garai
(University of Pennsylvania Perelman School of Medicine)
- Kenneth Hassinger
(University of Pennsylvania Perelman School of Medicine)
- Jingxuan Bao
(University of Pennsylvania Perelman School of Medicine)
- Junhao Wen
(University of Southern California)
- Duy Duong-Tran
(University of Pennsylvania Perelman School of Medicine
United States Naval Academy)
- Joost Wagenaar
(University of Pennsylvania Perelman School of Medicine)
- Michelle L. McKeague
(University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine)
- Mark M. Painter
(University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine)
- Divij Mathew
(University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine)
- Ajinkya Pattekar
(University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine)
- Nuala J. Meyer
(University of Pennsylvania)
- E. John Wherry
(University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine)
- Allison R. Greenplate
(University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine)
- Li Shen
(University of Pennsylvania Perelman School of Medicine)
Abstract
Recent advances in cytometry have enabled high-throughput data collection with multiple single-cell protein expression measurements. The significant biological and technical variance in cytometry has posed a formidable challenge during the gating process, especially for the initial pre-gates which deal with unpredictable events, such as debris and technical artifacts. To mitigate the labor-intensive manual gating process, we propose UNITO, a framework to rigorously identify the hierarchical cytometric subpopulations. UNITO transforms a cell-level classification task into an image-based segmentation problem. The framework is validated on three independent cohorts (two mass cytometry and one flow cytometry datasets). We compare its results with previous automated methods using the consensus of at least four experienced immunologists. UNITO outperforms existing methods and deviates from human consensus by no more than any individual does. UNITO can reproduce a similar contour compared to manual gating for post-hoc inspection, and it also allows parallelization of samples for faster processing.
Suggested Citation
Jiong Chen & Matei Ionita & Yanbo Feng & Yinfeng Lu & Patryk Orzechowski & Sumita Garai & Kenneth Hassinger & Jingxuan Bao & Junhao Wen & Duy Duong-Tran & Joost Wagenaar & Michelle L. McKeague & Mark , 2025.
"Automated cytometric gating with human-level performance using bivariate segmentation,"
Nature Communications, Nature, vol. 16(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-56622-2
DOI: 10.1038/s41467-025-56622-2
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