7-UP: Generating in silico CODEX from a small set of immunofluorescence markers

Author:

Wu Eric12ORCID,Trevino Alexandro E1,Wu Zhenqin13ORCID,Swanson Kyle4ORCID,Kim Honesty J1,D’Angio H Blaize1,Preska Ryan1,Chiou Aaron E1,Charville Gregory W5ORCID,Dalerba Piero6ORCID,Duvvuri Umamaheswar7ORCID,Colevas Alexander D8,Levi Jelena8,Bedi Nikita9,Chang Serena9,Sunwoo John9ORCID,Egloff Ann Marie10,Uppaluri Ravindra10,Mayer Aaron T1,Zou James12411ORCID

Affiliation:

1. Enable Medicine , Menlo Park, CA 94025 , USA

2. Department of Electrical Engineering, Stanford University , Stanford, CA 94305 , USA

3. Department of Chemistry, Stanford University , Stanford, CA 94305 , USA

4. Department of Computer Science, Stanford University , Stanford, CA 94305 , USA

5. Department of Pathology, Stanford University , Stanford, CA 94305 , USA

6. Department of Pathology and Cell Biology, Columbia University , New York, NY 10027 , USA

7. Department of Otolaryngology, University of Pittsburgh , Pittsburgh, PA 15213 , USA

8. CellSight Technologies , San Francisco, CA 94107 , USA

9. Department of Otolaryngology-Head and Neck Surgery, Stanford University , Stanford, CA 94305 , USA

10. Department of Medical Oncology, Dana-Farber Cancer Institute , Boston, MA 02215 , USA

11. Department of Biomedical Data Science, Stanford University , Stanford, CA 94305 , USA

Abstract

Abstract Multiplex immunofluorescence (mIF) assays multiple protein biomarkers on a single tissue section. Recently, high-plex CODEX (co-detection by indexing) systems enable simultaneous imaging of 40+ protein biomarkers, unlocking more detailed molecular phenotyping, leading to richer insights into cellular interactions and disease. However, high-plex data can be slower and more costly to collect, limiting its applications, especially in clinical settings. We propose a machine learning framework, 7-UP, that can computationally generate in silico 40-plex CODEX at single-cell resolution from a standard 7-plex mIF panel by leveraging cellular morphology. We demonstrate the usefulness of the imputed biomarkers in accurately classifying cell types and predicting patient survival outcomes. Furthermore, 7-UP's imputations generalize well across samples from different clinical sites and cancer types. 7-UP opens the possibility of in silico CODEX, making insights from high-plex mIF more widely available.

Funder

NSF

Knight-Hennessy Fellowship

Publisher

Oxford University Press (OUP)

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