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OrganoID: A versatile deep learning platform for tracking and analysis of single-organoid dynamics.
Matthews, Jonathan M; Schuster, Brooke; Kashaf, Sara Saheb; Liu, Ping; Ben-Yishay, Rakefet; Ishay-Ronen, Dana; Izumchenko, Evgeny; Shen, Le; Weber, Christopher R; Bielski, Margaret; Kupfer, Sonia S; Bilgic, Mustafa; Rzhetsky, Andrey; Tay, Savas.
Afiliação
  • Matthews JM; Pritzker School of Molecular Engineering, The University of Chicago, Chicago, Illinois, United States of America.
  • Schuster B; Institute for Genomics and Systems Biology, The University of Chicago, Chicago, Illinois, United States of America.
  • Kashaf SS; Pritzker School of Medicine, The University of Chicago, Chicago, Illinois, United States of America.
  • Liu P; Pritzker School of Molecular Engineering, The University of Chicago, Chicago, Illinois, United States of America.
  • Ben-Yishay R; Institute for Genomics and Systems Biology, The University of Chicago, Chicago, Illinois, United States of America.
  • Ishay-Ronen D; Department of Chemistry, The University of Chicago, Chicago, Illinois, United States of America.
  • Izumchenko E; Pritzker School of Molecular Engineering, The University of Chicago, Chicago, Illinois, United States of America.
  • Shen L; Institute for Genomics and Systems Biology, The University of Chicago, Chicago, Illinois, United States of America.
  • Weber CR; Pritzker School of Medicine, The University of Chicago, Chicago, Illinois, United States of America.
  • Bielski M; Department of Computer Science, Illinois Institute of Technology, Chicago, Illinois, United States of America.
  • Kupfer SS; Institute of Oncology, Sheba Medical Center, Ramat-Gan, Israel.
  • Bilgic M; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Rzhetsky A; Institute of Oncology, Sheba Medical Center, Ramat-Gan, Israel.
  • Tay S; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
PLoS Comput Biol ; 18(11): e1010584, 2022 11.
Article em En | MEDLINE | ID: mdl-36350878
Organoids have immense potential as ex vivo disease models for drug discovery and personalized drug screening. Dynamic changes in individual organoid morphology, number, and size can indicate important drug responses. However, these metrics are difficult and labor-intensive to obtain for high-throughput image datasets. Here, we present OrganoID, a robust image analysis platform that automatically recognizes, labels, and tracks single organoids, pixel-by-pixel, in brightfield and phase-contrast microscopy experiments. The platform was trained on images of pancreatic cancer organoids and validated on separate images of pancreatic, lung, colon, and adenoid cystic carcinoma organoids, which showed excellent agreement with manual measurements of organoid count (95%) and size (97%) without any parameter adjustments. Single-organoid tracking accuracy remained above 89% over a four-day time-lapse microscopy study. Automated single-organoid morphology analysis of a chemotherapy dose-response experiment identified strong dose effect sizes on organoid circularity, solidity, and eccentricity. OrganoID enables straightforward, detailed, and accurate image analysis to accelerate the use of organoids in high-throughput, data-intensive biomedical applications.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article