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

Title7-UP: Generating in silico CODEX from a small set of immunofluorescence markers
Authors
Issue Date2023
Citation
PNAS Nexus, 2023, v. 2, n. 6, article no. pgad171 How to Cite?
AbstractMultiplex 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.
Persistent Identifierhttp://hdl.handle.net/10722/354397
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWu, Eric-
dc.contributor.authorTrevino, Alexandro E.-
dc.contributor.authorWu, Zhenqin-
dc.contributor.authorSwanson, Kyle-
dc.contributor.authorKim, Honesty J.-
dc.contributor.authorD'Angio, H. Blaize-
dc.contributor.authorPreska, Ryan-
dc.contributor.authorChiou, Aaron E.-
dc.contributor.authorCharville, Gregory W.-
dc.contributor.authorDalerba, Piero-
dc.contributor.authorDuvvuri, Umamaheswar-
dc.contributor.authorColevas, Alexander D.-
dc.contributor.authorLevi, Jelena-
dc.contributor.authorBedi, Nikita-
dc.contributor.authorChang, Serena-
dc.contributor.authorSunwoo, John-
dc.contributor.authorEgloff, Ann Marie-
dc.contributor.authorUppaluri, Ravindra-
dc.contributor.authorMayer, Aaron T.-
dc.contributor.authorZou, James-
dc.date.accessioned2025-02-07T08:48:21Z-
dc.date.available2025-02-07T08:48:21Z-
dc.date.issued2023-
dc.identifier.citationPNAS Nexus, 2023, v. 2, n. 6, article no. pgad171-
dc.identifier.urihttp://hdl.handle.net/10722/354397-
dc.description.abstractMultiplex 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.-
dc.languageeng-
dc.relation.ispartofPNAS Nexus-
dc.title7-UP: Generating in silico CODEX from a small set of immunofluorescence markers-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1093/pnasnexus/pgad171-
dc.identifier.scopuseid_2-s2.0-85174046321-
dc.identifier.volume2-
dc.identifier.issue6-
dc.identifier.spagearticle no. pgad171-
dc.identifier.epagearticle no. pgad171-
dc.identifier.eissn2752-6542-
dc.identifier.isiWOS:001052638300003-

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