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7-UP: Generating in silico CODEX from a small set of immunofluorescence markers
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 cellula...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10236358/ https://www.ncbi.nlm.nih.gov/pubmed/37275261 http://dx.doi.org/10.1093/pnasnexus/pgad171 |
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author | Wu, Eric Trevino, Alexandro E Wu, Zhenqin Swanson, Kyle Kim, Honesty J D’Angio, H Blaize Preska, Ryan Chiou, Aaron E Charville, Gregory W Dalerba, Piero Duvvuri, Umamaheswar Colevas, Alexander D Levi, Jelena Bedi, Nikita Chang, Serena Sunwoo, John Egloff, Ann Marie Uppaluri, Ravindra Mayer, Aaron T Zou, James |
author_facet | Wu, Eric Trevino, Alexandro E Wu, Zhenqin Swanson, Kyle Kim, Honesty J D’Angio, H Blaize Preska, Ryan Chiou, Aaron E Charville, Gregory W Dalerba, Piero Duvvuri, Umamaheswar Colevas, Alexander D Levi, Jelena Bedi, Nikita Chang, Serena Sunwoo, John Egloff, Ann Marie Uppaluri, Ravindra Mayer, Aaron T Zou, James |
author_sort | Wu, Eric |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10236358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102363582023-06-03 7-UP: Generating in silico CODEX from a small set of immunofluorescence markers Wu, Eric Trevino, Alexandro E Wu, Zhenqin Swanson, Kyle Kim, Honesty J D’Angio, H Blaize Preska, Ryan Chiou, Aaron E Charville, Gregory W Dalerba, Piero Duvvuri, Umamaheswar Colevas, Alexander D Levi, Jelena Bedi, Nikita Chang, Serena Sunwoo, John Egloff, Ann Marie Uppaluri, Ravindra Mayer, Aaron T Zou, James PNAS Nexus Biological, Health, and Medical Sciences 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. Oxford University Press 2023-05-19 /pmc/articles/PMC10236358/ /pubmed/37275261 http://dx.doi.org/10.1093/pnasnexus/pgad171 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of National Academy of Sciences. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biological, Health, and Medical Sciences Wu, Eric Trevino, Alexandro E Wu, Zhenqin Swanson, Kyle Kim, Honesty J D’Angio, H Blaize Preska, Ryan Chiou, Aaron E Charville, Gregory W Dalerba, Piero Duvvuri, Umamaheswar Colevas, Alexander D Levi, Jelena Bedi, Nikita Chang, Serena Sunwoo, John Egloff, Ann Marie Uppaluri, Ravindra Mayer, Aaron T Zou, James 7-UP: Generating in silico CODEX from a small set of immunofluorescence markers |
title |
7-UP: Generating in silico CODEX from a small set of immunofluorescence markers |
title_full |
7-UP: Generating in silico CODEX from a small set of immunofluorescence markers |
title_fullStr |
7-UP: Generating in silico CODEX from a small set of immunofluorescence markers |
title_full_unstemmed |
7-UP: Generating in silico CODEX from a small set of immunofluorescence markers |
title_short |
7-UP: Generating in silico CODEX from a small set of immunofluorescence markers |
title_sort | 7-up: generating in silico codex from a small set of immunofluorescence markers |
topic | Biological, Health, and Medical Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10236358/ https://www.ncbi.nlm.nih.gov/pubmed/37275261 http://dx.doi.org/10.1093/pnasnexus/pgad171 |
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