Back Cover: A novel multiphoton microscopy images segmentation method based on superpixel and watershed (J. Biophotonics 4/2017)

2017 ◽  
Vol 10 (4) ◽  
pp. 608-608
2016 ◽  
Vol 10 (4) ◽  
pp. 532-541 ◽  
Author(s):  
Weilin Wu ◽  
Jinyong Lin ◽  
Shu Wang ◽  
Yan Li ◽  
Mingyu Liu ◽  
...  

2011 ◽  
Author(s):  
Kevin S. Lorenz ◽  
Paul Salama ◽  
Kenneth W. Dunn ◽  
Edward J. Delp

2021 ◽  
Vol 12 (1) ◽  
pp. 27
Author(s):  
Elena Terradillos ◽  
CristinaL Saratxaga ◽  
Sara Mattana ◽  
Riccardo Cicchi ◽  
FrancescoS Pavone ◽  
...  

Photonics ◽  
2021 ◽  
Vol 8 (12) ◽  
pp. 573
Author(s):  
Juan M. Bueno ◽  
Geovanni Hernández ◽  
Martin Skorsetz ◽  
Pablo Artal

Multiphoton (MP) microscopy is a well-established method for the non-invasive imaging of biological tissues. However, its optical sectioning capabilities are reduced due to specimen-induced aberrations. Both the manipulation of spherical aberration (SA) and the use of axicons have been reported to be useful techniques to bypass this limitation. We propose the combination of SA patterns and variable axicons to further improve the quality of MP microscopy images. This approach provides enhanced images at different depth locations whose quality is better than those corresponding to the use of SA or axicons separately. Thus, the procedure proposed herein facilitates the visualization of details and increases the depth observable at high resolution.


Author(s):  
Carsen Stringer ◽  
Tim Wang ◽  
Michalis Michaelos ◽  
Marius Pachitariu

Many biological applications require the segmentation of cell bodies, membranes and nuclei from microscopy images. Deep learning has enabled great progress on this problem, but current methods are specialized for images that have large training datasets. Here we introduce a generalist, deep learning-based segmentation method called Cellpose, which can precisely segment cells from a wide range of image types and does not require model retraining or parameter adjustments. We trained Cellpose on a new dataset of highly-varied images of cells, containing over 70,000 segmented objects. We also demonstrate a 3D extension of Cellpose which reuses the 2D model and does not require 3D-labelled data. To support community contributions to the training data, we developed software for manual labelling and for curation of the automated results, with optional direct upload to our data repository. Periodically retraining the model on the community-contributed data will ensure that Cellpose improves constantly.


2018 ◽  
Vol 23 (06) ◽  
pp. 1 ◽  
Author(s):  
Mikko J. Huttunen ◽  
Abdurahman Hassan ◽  
Curtis W. McCloskey ◽  
Sijyl Fasih ◽  
Jeremy Upham ◽  
...  

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