unrolling a z-stack

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unrolling a z-stack

Elizabeth Crowell
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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Re: unrolling a z-stack

Bill Mohler
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
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Fax: (314) 689-1833

G&DB dept. ofc.: (860) 679-8350
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http://genetics.uchc.edu/Faculty/Mohler/Mohler.html
P Think before you print
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Re: unrolling a z-stack

Julian Cooper
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
>