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Deep learning for label-free nuclei detection from implicit phase information of mesenchymal stem cells.
Zhang, Zhengyun; Leong, Kim Whye; Vliet, Krystyn Van; Barbastathis, George; Ravasio, Andrea.
Afiliación
  • Zhang Z; BioSyM IRG, Singapore-MIT Alliance for Research and Technology (SMART) Centre, 1 CREATE Way, #04-13/14 Enterprise Wing, Singapore 138602, Singapore.
  • Leong KW; zaltor@gmail.com.
  • Vliet KV; Department of Biological Sciences, National University of Singapore, 16 Science Drive 4, Singapore 117558, Singapore.
  • Barbastathis G; BioSyM IRG, Singapore-MIT Alliance for Research and Technology (SMART) Centre, 1 CREATE Way, #04-13/14 Enterprise Wing, Singapore 138602, Singapore.
  • Ravasio A; Department of Materials Science and Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.
Biomed Opt Express ; 12(3): 1683-1706, 2021 Mar 01.
Article en En | MEDLINE | ID: mdl-33796381
ABSTRACT
Monitoring of adherent cells in culture is routinely performed in biological and clinical laboratories, and it is crucial for large-scale manufacturing of cells needed in cell-based clinical trials and therapies. However, the lack of reliable and easily implementable label-free techniques makes this task laborious and prone to human subjectivity. We present a deep-learning-based processing pipeline that locates and characterizes mesenchymal stem cell nuclei from a few bright-field images captured at various levels of defocus under collimated illumination. Our approach builds upon phase-from-defocus methods in the optics literature and is easily applicable without the need for special microscopy hardware, for example, phase contrast objectives, or explicit phase reconstruction methods that rely on potentially bias-inducing priors. Experiments show that this label-free method can produce accurate cell counts as well as nuclei shape statistics without the need for invasive staining or ultraviolet radiation. We also provide detailed information on how the deep-learning pipeline was designed, built and validated, making it straightforward to adapt our methodology to different types of cells. Finally, we discuss the limitations of our technique and potential future avenues for exploration.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Biomed Opt Express Año: 2021 Tipo del documento: Article País de afiliación: Singapur

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Biomed Opt Express Año: 2021 Tipo del documento: Article País de afiliación: Singapur