4.7 Article

Object detection networks and augmented reality for cellular detection in fluorescence microscopy

期刊

JOURNAL OF CELL BIOLOGY
卷 219, 期 10, 页码 -

出版社

ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.201903166

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资金

  1. UK Research and Innovation Biotechnology and Biological Sciences Research Council [BB/P026354/1]
  2. UK Research and Innovation Molecular Research Council [MR/S005382/1a, MC_UU_12009, MC_UU_12010, G0902418, MC_UU_12025, MR/K01577X/1]
  3. EPA Cephalosporin Fund
  4. Wellcome Trust [104924/14/Z/14, 091911]
  5. Wolfson Foundation
  6. John Fell Fund
  7. Deutsche Forschungsgemeinschaft (Research Unit 1905 Structure and function of the peroxisomal translocon)
  8. Deutsche Forschungsgemeinschaft (Jena Excellence Cluster Balance of the Microverse)
  9. Deutsche Forschungsgemeinschaft (Collaborative Research Center 1278 Polytarget)
  10. BBSRC [BB/P026354/1] Funding Source: UKRI
  11. MRC [MC_UU_00016/1, MC_UU_00008/9, MR/S005382/1] Funding Source: UKRI

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Object detection networks are high-performance algorithms famously applied to the task of identifying and localizing objects in photography images. We demonstrate their application for the classification and localization of cells in fluorescence microscopy by benchmarking four leading object detection algorithms across multiple challenging 2D microscopy datasets. Furthermore we develop and demonstrate an algorithm that can localize and image cells in 3D, in close to real time, at the microscope using widely available and inexpensive hardware. Furthermore, we exploit the fast processing of these networks and develop a simple and effective augmented reality (AR) system for fluorescence microscopy systems using a display screen and back-projection onto the eyepiece. We show that it is possible to achieve very high classification accuracy using datasets with as few as 26 images present. Using our approach, it is possible for relatively nonskilled users to automate detection of cell classes with a variety of appearances and enable new avenues for automation of fluorescence microscopy acquisition pipelines.

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