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Three-dimensional residual channel attention networks denoise and sharpen fluorescence microscopy image volumes.
Chen, Jiji; Sasaki, Hideki; Lai, Hoyin; Su, Yijun; Liu, Jiamin; Wu, Yicong; Zhovmer, Alexander; Combs, Christian A; Rey-Suarez, Ivan; Chang, Hung-Yu; Huang, Chi Chou; Li, Xuesong; Guo, Min; Nizambad, Srineil; Upadhyaya, Arpita; Lee, Shih-Jong J; Lucas, Luciano A G; Shroff, Hari.
Afiliación
  • Chen J; Advanced Imaging and Microscopy Resource, National Institutes of Health, Bethesda, MD, USA. jiji.chen@nih.gov.
  • Sasaki H; Leica Microsystems, Inc., Buffalo Grove, IL, USA. hideki.sasaki@aivia-software.com.
  • Lai H; SVision LLC, Bellevue, WA, USA. hideki.sasaki@aivia-software.com.
  • Su Y; Leica Microsystems, Inc., Buffalo Grove, IL, USA.
  • Liu J; SVision LLC, Bellevue, WA, USA.
  • Wu Y; Advanced Imaging and Microscopy Resource, National Institutes of Health, Bethesda, MD, USA.
  • Zhovmer A; Leica Microsystems, Inc., Buffalo Grove, IL, USA.
  • Combs CA; SVision LLC, Bellevue, WA, USA.
  • Rey-Suarez I; Laboratory of High Resolution Optical Imaging, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, MD, USA.
  • Chang HY; Advanced Imaging and Microscopy Resource, National Institutes of Health, Bethesda, MD, USA.
  • Huang CC; Laboratory of High Resolution Optical Imaging, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, MD, USA.
  • Li X; Laboratory of Molecular Cardiology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
  • Guo M; NHLBI Light Microscopy Facility, National Institutes of Health, Bethesda, MD, USA.
  • Nizambad S; Biophysics Program, University of Maryland, College Park, MD, USA.
  • Upadhyaya A; Institute for Physical Science and Technology, University of Maryland, College Park, MD, USA.
  • Lee SJ; Leica Microsystems, Inc., Buffalo Grove, IL, USA.
  • Lucas LAG; SVision LLC, Bellevue, WA, USA.
  • Shroff H; Leica Microsystems, Inc., Buffalo Grove, IL, USA.
Nat Methods ; 18(6): 678-687, 2021 06.
Article en En | MEDLINE | ID: mdl-34059829
ABSTRACT
We demonstrate residual channel attention networks (RCAN) for the restoration and enhancement of volumetric time-lapse (four-dimensional) fluorescence microscopy data. First we modify RCAN to handle image volumes, showing that our network enables denoising competitive with three other state-of-the-art neural networks. We use RCAN to restore noisy four-dimensional super-resolution data, enabling image capture of over tens of thousands of images (thousands of volumes) without apparent photobleaching. Second, using simulations we show that RCAN enables resolution enhancement equivalent to, or better than, other networks. Third, we exploit RCAN for denoising and resolution improvement in confocal microscopy, enabling ~2.5-fold lateral resolution enhancement using stimulated emission depletion microscopy ground truth. Fourth, we develop methods to improve spatial resolution in structured illumination microscopy using expansion microscopy data as ground truth, achieving improvements of ~1.9-fold laterally and ~3.6-fold axially. Finally, we characterize the limits of denoising and resolution enhancement, suggesting practical benchmarks for evaluation and further enhancement of network performance.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Microscopía Fluorescente Idioma: En Revista: Nat Methods Asunto de la revista: TECNICAS E PROCEDIMENTOS DE LABORATORIO Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Microscopía Fluorescente Idioma: En Revista: Nat Methods Asunto de la revista: TECNICAS E PROCEDIMENTOS DE LABORATORIO Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos