Sparse deconvolution App

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Official MATLAB implementation of the "Sparse deconvolution" -v1.0.3

View the Project on GitHub WeisongZhao/Sparse-SIM

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Sparse deconvolutionv1.0.3

Words written in the front: Physical resolution might be meaningless if in the mathmetical space.

It is a part of publication. For details, please refer to: Weisong Zhao et al. Sparse deconvolution improves the resolution of live-cell super-resolution fluorescence microscopy, Nature Biotechnology 40, 606–617 (2022).<hr>

The related Python version can be found at HERE

You can also find some fancy results and comparisons on my website.

If you are interested in our work, I wrote a #behind_the_paper post for further reading.

Here is also a blog about it for further reading.

This method has been tested on various types of Confocal microscopy & STED microscopy, Wide-field & TIRF microscopy, Light-sheet microscopy, Multi-photon microscopy, and Structured illumination microscopy, feasible for single-slice, time-lapse, and volumetric datasets.

Introduction

This repository contains the updating version of Sparse deconvolution. The Sparse deconvolution is an universal post-processing framework for fluorescence (or intensity-based) image restoration, including xy (2D), xy-t (2D along t axis), and xy-z (3D) images. It is based on the natural priori knowledge of forward fluorescence imaging model: sparsity and continuity along xy-t (z) axes.

Instruction

Installation of binary executable file (.exe) for Win10 system.

[](https://www.youtube.com/watch?v=99CoWvTtQwg “”)

Or directly click the .\for Maltab users\Sparse_SIM.exe if you are using MATLAB 2017b.

Algorithm UI

Parameters: Wiki and Document

Tested platform

This software has been tested on:

More on Wiki.

Version

Plans
  • Debug mode for parameter-adjustment;
  • A Pyhton version of Sparse deconvolution;
  • A imagej-plugin of Sparse deconvolution;
  • A Headless mode;
  • Reduce the necessary/exposed parameters.
  • Open source Sparse deconvolution