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Localisation Microscopy


We have developed a MATLAB application for Localisation Microscopy image processing, with a simple GUI interface. This application is a set of MATLAB scripts and functions, named rainSTORM, was developed as part of our super-resolution research in collaboration with the Biophysics Group at the National Physical Laboratory and the Advanced Optical Imaging Group at the University of Szeged.

Rees EJ, Erdelyi M, Kaminski-Schierle GS, Knight AE and Kaminski CF, "Elements of image processing in localisation microscopy", Journal of Optics 15, 094012 (2013). DOI | pdf | summary

download (v2.39) | download (v2.37) | User Guide 

Structured Illumination Microscopy

Joint-Richardson Lucy algorithm

We have developed a MATLAB application for multifocal structured illumination microscopy (MSIM) image reconstruction based on joint Richardson-Lucy deconvolution, named jRL-MSIM. This application is a set of MATLAB scripts and functions and was developed as part of our super-resolution research. The software package is easy to use due to its simple GUI and explained in detail in the respective publication and the accompanying manual.

Stroehl F, Kaminski C F, "A Joint Richardson-Lucy Deconvolution Algorithm for the Reconstruction of Multifocal Structured Illumination Microscopy Data." (2015) , Methods and Applications in Fluorescence 3 014002 DOI pdf summary


Fluorescence Lifetime Imaging (FLIM)

Multichannel FLIM-FRET analysis

We have developed matlab code for Multichannel FLIM-FRET analysis. It takes advantage of the linear properties of the phasor plot approach, and is able to recover the bound fractions of donors and acceptors in a FRET measurement. The software can be applied to recover the dissociation constant of binding reactions, the concentration of binding partners and the concentration of competitors for the binding. The theory and method used in this software is explained in detail in the publication and accompanying material.

Chen WY, Avezov E, Schlachter S C, Gielen F, Laine R F, Harding H P, Hollfelder F, Ron D and Kaminski C F, "A Method to Quantify FRET Stoichiometry with Phasor Plot Analysis and Acceptor Lifetime In-growth," Biophysical Journal (2015), 108 (5), 2015, pp. 999-1002DOI pdf | summary


Spectral Imaging of FRET

Sensitised Emission FRET  (seFRET)

This Matlab code is provided to accompany a book chapter on seFRET. In this technique, the fluorescence emission of a specimen in different spectral channels is affected by a contribution from FRET (resonant energy transfer) between two different fluorophores, as well as by the direct emission of each species. This analysis software quantifies the donor-normalised and acceptor-normalised FRET by analysing fluorescence intensity image data in two colour channels (sample data is included). 

Kaminski CF, Rees EJ, Schierle GS, "A quantitative protocol for intensity-based live cell FRET imaging". Methods Mol Biology (2014), 1076:445-454  DOI |pdf summary  


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