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Automated spatial omics landscape analysis approach reveals novel tissue architectures in ulcerative colitis.
Holman, Derek R; Rubin, Samuel J S; Ferenc, Mariusz; Holman, Elizabeth A; Koron, Alexander N; Daniel, Robel; Boland, Brigid S; Nolan, Garry P; Chang, John T; Rogalla, Stephan.
Afiliação
  • Holman DR; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University, Stanford, CA, USA. drholman@stanford.edu.
  • Rubin SJS; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University, Stanford, CA, USA.
  • Ferenc M; Nalecz Institute of Biocybernetics and Biomedical Engineering, Polish Academy of Sciences, Warsaw, Poland.
  • Holman EA; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University, Stanford, CA, USA.
  • Koron AN; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University, Stanford, CA, USA.
  • Daniel R; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University, Stanford, CA, USA.
  • Boland BS; Division of Gastroenterology, Department of Medicine, University of California San Diego, San Diego, CA, USA.
  • Nolan GP; Department of Pathology, Stanford University, Stanford, CA, USA.
  • Chang JT; Division of Gastroenterology, Department of Medicine, University of California San Diego, San Diego, CA, USA.
  • Rogalla S; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University, Stanford, CA, USA. srogalla@stanford.edu.
Sci Rep ; 14(1): 18934, 2024 08 15.
Article em En | MEDLINE | ID: mdl-39147769
ABSTRACT
The utility of spatial omics in leveraging cellular interactions in normal and diseased states for precision medicine is hampered by a lack of strategies for matching disease states with spatial heterogeneity-guided cellular annotations. Here we use a spatial context-dependent approach that matches spatial pattern detection to cell annotation. Using this approach in existing datasets from ulcerative colitis patient colonic biopsies, we identified architectural complexities and associated difficult-to-detect rare cell types in ulcerative colitis germinal-center B cell follicles. Our approach deepens our understanding of health and disease pathogenesis, illustrates a strategy for automating nested architecture detection for highly multiplexed spatial biology data, and informs precision diagnosis and therapeutic strategies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Colite Ulcerativa Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Colite Ulcerativa Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos