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Deep learning enables cross-modality super-resolution in fluorescence microscopy.
Wang, Hongda; Rivenson, Yair; Jin, Yiyin; Wei, Zhensong; Gao, Ronald; Günaydin, Harun; Bentolila, Laurent A; Kural, Comert; Ozcan, Aydogan.
Afiliação
  • Wang H; Electrical and Computer Engineering Department, University of California, Los Angeles, CA, USA.
  • Rivenson Y; Bioengineering Department, University of California, Los Angeles, CA, USA.
  • Jin Y; California NanoSystems Institute, University of California, Los Angeles, CA, USA.
  • Wei Z; Electrical and Computer Engineering Department, University of California, Los Angeles, CA, USA.
  • Gao R; Bioengineering Department, University of California, Los Angeles, CA, USA.
  • Günaydin H; California NanoSystems Institute, University of California, Los Angeles, CA, USA.
  • Bentolila LA; Electrical and Computer Engineering Department, University of California, Los Angeles, CA, USA.
  • Kural C; Electrical and Computer Engineering Department, University of California, Los Angeles, CA, USA.
  • Ozcan A; Computer Science Department, University of California, Los Angeles, CA, USA.
Nat Methods ; 16(1): 103-110, 2019 01.
Article em En | MEDLINE | ID: mdl-30559434
ABSTRACT
We present deep-learning-enabled super-resolution across different fluorescence microscopy modalities. This data-driven approach does not require numerical modeling of the imaging process or the estimation of a point-spread-function, and is based on training a generative adversarial network (GAN) to transform diffraction-limited input images into super-resolved ones. Using this framework, we improve the resolution of wide-field images acquired with low-numerical-aperture objectives, matching the resolution that is acquired using high-numerical-aperture objectives. We also demonstrate cross-modality super-resolution, transforming confocal microscopy images to match the resolution acquired with a stimulated emission depletion (STED) microscope. We further demonstrate that total internal reflection fluorescence (TIRF) microscopy images of subcellular structures within cells and tissues can be transformed to match the results obtained with a TIRF-based structured illumination microscope. The deep network rapidly outputs these super-resolved images, without any iterations or parameter search, and could serve to democratize super-resolution imaging.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microscopia Confocal / Aprendizado Profundo / Microscopia de Fluorescência Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microscopia Confocal / Aprendizado Profundo / Microscopia de Fluorescência Idioma: En Ano de publicação: 2019 Tipo de documento: Article