Dear ImageJ experts,
I am taking images of fibers that occur on the periphery of cells, and acquiring z-stacks of the entire cell. The cells are roughly cylindrical. For visualization purposes, it would be useful to virtually slice open these cells and unroll them so that I can see the fibers on every face of the cylinder in the same plane. Is there a means of doing this? Has anyone encountered this issue before? Segmentation of the cells should not be a problem, since I can simply delete the signal outside of the cells in each slice. (This does not need to be a high-through-put procedure.) Thank you in advance for your ideas... Sincerely, Elizabeth Crowell Laboratoire de Biologie Cellulaire INRA / Institut Jean-Pierre Bourgin Route de Saint-Cyr 78026 Versailles cedex FRANCE Tel: (33) 01.30.83.30.21 Fax: (33) 01.30.83.30.99 |
I would suggest rotating projections around the y-axis
(Image>Stack>3dProject), followed by cropping to a small central region for each projection image, and then use of some sort of stitching software to build the whole "panorama". There is a whole field of panoramic photographic rendering that also has listservs that might help with the stitching details. There may also be ImageJ plugins to do the work. Elizabeth Crowell wrote: > Dear ImageJ experts, > > I am taking images of fibers that occur on the periphery of cells, and acquiring > z-stacks of the entire cell. The cells are roughly cylindrical. > For visualization purposes, it would be useful to virtually slice open these > cells and unroll them so that I can see the fibers on every face of the > cylinder in the same plane. > Is there a means of doing this? Has anyone encountered this issue before? > > Segmentation of the cells should not be a problem, since I can simply delete the > signal outside of the cells in each slice. (This does not need to be a > high-through-put procedure.) > > Thank you in advance for your ideas... > > Sincerely, > > Elizabeth Crowell > Laboratoire de Biologie Cellulaire > INRA / Institut Jean-Pierre Bourgin > Route de Saint-Cyr > 78026 Versailles cedex > FRANCE > > Tel: (33) 01.30.83.30.21 > Fax: (33) 01.30.83.30.99 > > -- William A. Mohler Associate Professor Dept. of Genetics and Developmental Biology University of Connecticut Health Center MC-3301 263 Farmington Ave. Farmington, CT 06030-3301 [hidden email] *Mobile: (860) 985-2719* alt. mobile: (860) 331-8514 skype: wmohler Office: (860) 679-1833, room E2029 Lab: (860) 679-1834, room E2032 Fax: (314) 689-1833 G&DB dept. ofc.: (860) 679-8350 G&DB dept. fax : (860) 679-8345 http://genetics.uchc.edu/Faculty/Mohler/Mohler.html P Think before you print |
In reply to this post by Elizabeth Crowell
Hi Elizabeth,
If I understand your problem correctly you can achieve this with the Radial Reslice plugin: http://rsb.info.nih.gov/ij/plugins/radial-reslice/index.html Start with a line selection with the initial end on the centre of the cell and use the plugin to rotate 360° about that end. This will give you a stack of slices of the cell rotated about the centre. If you reslice (Image>Stacks>Reslice or press '/') this resulting stack from the right or left the peripheral fibres should be displayed in the stack as you require. I use this technique to "unroll" cylindrical bones to visualise the pattern of a fracture or non-union. I hope this helps. Kind regards, Julian > -----Original Message----- > From: ImageJ Interest Group [mailto:[hidden email]] On > Behalf Of Elizabeth Crowell > Sent: 15 October 2009 16:26 > To: [hidden email] > Subject: unrolling a z-stack > > > Dear ImageJ experts, > > I am taking images of fibers that occur on the periphery of > cells, and acquiring > z-stacks of the entire cell. The cells are roughly cylindrical. > For visualization purposes, it would be useful to virtually > slice open these > cells and unroll them so that I can see the fibers on every > face of the > cylinder in the same plane. > Is there a means of doing this? Has anyone encountered this > issue before? > > Segmentation of the cells should not be a problem, since I > can simply delete the > signal outside of the cells in each slice. (This does not > need to be a > high-through-put procedure.) > > Thank you in advance for your ideas... > > Sincerely, > > Elizabeth Crowell > Laboratoire de Biologie Cellulaire > INRA / Institut Jean-Pierre Bourgin > Route de Saint-Cyr > 78026 Versailles cedex > FRANCE > > Tel: (33) 01.30.83.30.21 > Fax: (33) 01.30.83.30.99 > |
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