Flow and mass cytometry provide multiparametric single-cell data critical for understanding the cellular heterogeneity in various biological systems. Modern polychromatic flow cytometers simultaneously measure about 16 parameters routinely. The next-generation mass cytometry (CyTOF) technology allows for the simultaneous measurement of 50 or more parameters. Even as the cytometry technology is rapidly advancing, approaches for analyzing such complex data remain inadequate. The widely-used manual gating analysis is knowledge-driven and easy-to- interpret, but it is subjective, labor-intensive, and not scalable to handle the increasing complexity of the data. Recent developments of automated data-driven algorithms are able to address the issues of manual gating, but the results from data-driven algorithms are often not intuitive for biology experts to interpret. These limitations create a critical bottleneck for flow and mass cytometry analysis. The overall objective of this application is to develop a novel framework that combines both knowledge-driven and data-driven approaches to achieve automated gating analysis of flow cytometry and CyTOF data.
The specific aims are: (1) build knowledge graphs to capture existing knowledge of manual gating analysis, (2) develop algorithms for automated gating analysis, and (3) validate the knowledge graph framework using large-scale studies in ImmPort. The proposed research is significant because it will enable efficient and reproducible gating analysis and provide visualizations that are easy-to-interpret, both of which are critically important to the research community. Such contributions will fundamentally impact single-cell analysis of cellular heterogeneity in diverse fields including immunology, infectious diseases, cancer, AIDS, among others.

Public Health Relevance

The proposed research is relevant to public health because it is expected to develop novel computational methods for automated analysis and interpretation of single-cell analysis by flow and mass cytometry. Such contributions will impact single-cell analysis of cellular heterogeneity in diverse fields such as immunology, infectious diseases, cancer, AIDS, among others.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Cooperative Agreement Phase I (UH2)
Project #
1UH2AI153028-01
Application #
10026829
Study Section
Special Emphasis Panel (ZAI1)
Program Officer
Chen, Quan
Project Start
2020-06-01
Project End
2022-05-31
Budget Start
2020-06-01
Budget End
2021-05-31
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Georgia Institute of Technology
Department
Engineering (All Types)
Type
Biomed Engr/Col Engr/Engr Sta
DUNS #
097394084
City
Atlanta
State
GA
Country
United States
Zip Code
30332