scholarly journals Bayesian cluster identification in single-molecule localization microscopy data

2015 ◽  
Vol 12 (11) ◽  
pp. 1072-1076 ◽  
Author(s):  
Patrick Rubin-Delanchy ◽  
Garth L Burn ◽  
Juliette Griffié ◽  
David J Williamson ◽  
Nicholas A Heard ◽  
...  
2016 ◽  
Vol 11 (12) ◽  
pp. 2499-2514 ◽  
Author(s):  
Juliette Griffié ◽  
Michael Shannon ◽  
Claire L Bromley ◽  
Lies Boelen ◽  
Garth L Burn ◽  
...  

2019 ◽  
Vol 20 (1) ◽  
Author(s):  
Maarten W. Paul ◽  
H. Martijn de Gruiter ◽  
Zhanmin Lin ◽  
Willy M. Baarends ◽  
Wiggert A. van Cappellen ◽  
...  

2020 ◽  
Author(s):  
Magdalena C. Schneider ◽  
Roger Telschow ◽  
Gwenael Mercier ◽  
Montserrat López-Martinez ◽  
Otmar Scherzer ◽  
...  

ABSTRACTSingle molecule localization microscopy (SMLM) has enormous potential for resolving subcellular structures below the diffraction limit of light microscopy: Localization precision in the low digit nanometer regime has been shown to be achievable. In order to record localization microscopy data, however, sample fixation is inevitable to prevent molecular motion during the rather long recording times of minutes up to hours. Eventually, it turns out that preservation of the sample’s ultrastructure during fixation becomes the limiting factor. We propose here a workflow for data analysis, which is based on SMLM performed at cryogenic temperatures. Since molecular dipoles of the fluorophores are fixed at low temperatures, such an approach offers the possibility to use the orientation of the dipole as an additional information for image analysis. In particular, assignment of localizations to individual dye molecules becomes possible with high reliability. We quantitatively characterized the new approach based on the analysis of simulated oligomeric structures. Side lengths can be determined with a relative error of less than 1% for tetramers with a nominal side length of 5 nm, even if the assumed localization precision for single molecules is more than 2 nm.


2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Ruby Peters ◽  
Juliette Griffié ◽  
Garth L. Burn ◽  
David J. Williamson ◽  
Dylan M. Owen

2011 ◽  
Vol 137 (1) ◽  
pp. 1-10 ◽  
Author(s):  
Sebastian Malkusch ◽  
Ulrike Endesfelder ◽  
Justine Mondry ◽  
Márton Gelléri ◽  
Peter J. Verveer ◽  
...  

2021 ◽  
Author(s):  
Jiachuan Bai ◽  
Wei Ouyang ◽  
Manish Kumar Singh ◽  
Christophe Leterrier ◽  
Paul Barthelemy ◽  
...  

Novel insights and more powerful analytical tools can emerge from the reanalysis of existing data sets, especially via machine learning methods. Despite the widespread use of single molecule localization microscopy (SMLM) for super-resolution bioimaging, the underlying data are often not publicly accessible. We developed ShareLoc (https://shareloc.xyz), an open platform designed to enable sharing, easy visualization and reanalysis of SMLM data. We discuss its features and show how data sharing can improve the performance and robustness of SMLM image reconstruction by deep learning.


2018 ◽  
Author(s):  
Hazen P. Babcock ◽  
Fang Huang

ABSTRACTOptimal analysis of single molecule localization microscopy (SMLM) data acquired with a CMOS camera requires compensation for single pixel differences in gain, offset and readout noise. For some CMOS cameras we found that it is also necessary to compensate for pixel differences in sensitivity or relative quantum efficiency (RQE). We present the modifications to the original sCMOS analysis algorithm necessary to correct for these RQE differences. We also discuss the use of the Anscombe transform (AT) for variance stabilization. Removing the variance dependence on the mean allows simpler least squares fitting approaches to achieve the Cramer-Rao bound on the mixed Poisson and Gaussian distributed data typically acquired with an sCMOS camera.


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