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).
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.
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.
Install.m
Effective NA
should be given according to the sum of illumination NA
and detection NA
. For instances: wide-field is the objective NA
(e.g., 1.49); SIM is the illumination NA + objective NA
(e.g., 1.3 + 1.7); SD-SIM is ~1.8 * objective NA
.xxx
to get the API.
help SparseHessian_core
help background_estimation
help Fourier_Oversample
.\for Maltab users\Sparse_SIM.exe
if you are using MATLAB 2017b.
This software has been tested on:
More on Wiki.
.mat
to .tif