Data is organised into 3 sub-directories, 1 for each imaging experiment (beads, lens-tissue and chloroplasts). 

Each of these sub-directories contains 3 further sub-directories, holding the PSF data, raw snapshot images and deconvolved/reconstructed volumes.

There is also a Jupyter (python) notebook for each experiment containing code for processing and deconvolution of data.


Image (.tif) data can be opened with any .tif image reader, e.g. Fiji/ImageJ.