Hi Esteban and all,
I have been testing Piotr W's deconv plugins this week with some interesting results. I used the versions (1.9) from the link on the Fiji wiki page for parallel and spectral iterative deconvolution. I just put the .jars in the Fiji plugins dir manually. I made PSFs with the Diffraction PSF 3D plugin from Bob D and convolved ground truth images with the Convolve 3D plugin also from Bob D. I also tested Bobs Iterative Deconvlove 3D plugin (runs on a single thread) With the bat cochlea volume sample data set, convolved with a theoretical PSF, added gaussian noise, then deconvolved with the same PSF, i got the most sensible results using the Parallel Iterative Deconvolution WPL method (100 max iterations, single precision, reflexive boundary .... default settings) This looked very similar to the result from Bob's Iterative Deconvolve 3D, as one might expect as its pretty much the same method, just parallelised. On a 8 core machine it's pretty fast..... I also got a reasonable result with the Parallel Spectral Deconvolution Generalized Tikhonov (reflexive), Laplacian, threshold 0, auto regularization. This gave a result with possibly more artifacts (only low intensities, nothing really really bad) but is super super fast on a machine with 8 cores. More time is spent in the setup and pre calculation steps that the actual doconv it seems. Its a bit quick and dirty maybe, but sometimes thats the best you can do anyway (noisy data?) and it might be good enough for some tasks...(not intensity analysis perhaps) On real fluorescence microscopy data I also got reasonable results using these methods. Note the default MRNSD method didnt seem to do as good a job on my ground truth data as the WPL method. Maybe there is more to be investigated there. Note that Bobs diffraction psf 3d plugin generates widefield PSFs only. For a confocal PSF... well you can approximate it by making the square of a widefield one... but i'm not sure how good that is. There is a thread about that currently running on the ImageJ list... subject = Confocal PSF (was Puncta quantitation) Generally, measured PSF is nearly always the best (but sometimes overkill for very noisy data?) Lenses and other optics are often far from perfect and a theoretical PSF may be way off the real one of the system. cheers Dan > "G. Esteban Fernandez" <[hidden email]> Apr 05 > 11:10AM -0700 ^ > > Hello, > > I just installed Fiji primarily to use the Parallel Iterative > Deconvolution plugin that it implements, but I don’t see it anywhere. > Can someone help me out please? > > Thanks, > Esteban > > -- > G. Esteban Fernandez, Ph.D. > Imaging Scientist > > Cellular Imaging Core > Childrens Hospital Los Angeles Dr. Daniel James White BSc. (Hons.) PhD Senior Microscopist / Image Visualisation, Processing and Analysis Light Microscopy and Image Processing Facilities Max Planck Institute of Molecular Cell Biology and Genetics Pfotenhauerstrasse 108 01307 DRESDEN Germany +49 (0)15114966933 (German Mobile) +49 (0)351 210 2627 (Work phone at MPI-CBG) +49 (0)351 210 1078 (Fax MPI-CBG LMF) http://www.bioimagexd.net BioImageXD http://pacific.mpi-cbg.de Fiji - is just ImageJ (Batteries Included) http://www.chalkie.org.uk Dan's Homepages https://ifn.mpi-cbg.de Dresden Imaging Facility Network dan (at) chalkie.org.uk ( white (at) mpi-cbg.de ) |
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