Posted by
Thomas Boudier on
URL: http://imagej.273.s1.nabble.com/How-to-select-object-volume-in-3d-stack-tp4999044p4999059.html
Hello,
The 3D tools you may have a look for 3D segmentation and analysis, also
manual segmentation :
http://imagejdocu.tudor.lu/doku.php?id=plugin:analysis:3d_object_counter:starthttp://imagejdocu.tudor.lu/doku.php?id=plugin:stacks:3d_roi_manager:starthttp://132.187.25.13/home/?category=Download&page=SegmentationEditorhope this helps
Thomas
Le 13/06/2012 21:05, Bruce Citron a écrit :
> In a single slice, I can easily: 1. Threshold, then 2. Use the wand tool to
> select an irregular region of interest, e.g., an irregularly shaped cell in
> a micrograph.
> I am having trouble doing this for a 3d confocal stack. I can threshold so
> that in all slices, the cell is all red.
>
> € How would I then perform the equivalent of the wand tool selections so
> that all of the cell, in each z-slice, would be outlined and selected?
> It would be like a seed fill, where all of the connected thresholded voxels
> are connected into an irregular 3d ROI.
> I would then want to determine volume and mean intensity.
>
> I usually want to ignore other cells in the same image, but I would also be
> interested in a 3d particle analysis with count, volumes and mean
> intensities.
>
> I tried Yawi3d, but I couldn¹t seem to get it to do what I wanted.
> Thank you,
> Bruce
> --
> Bruce A. Citron, Ph.D., Bay Pines VA
>
>
> --
> ImageJ mailing list:
http://imagej.nih.gov/ij/list.html>
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Thomas Boudier, MCU Université Pierre et Marie Curie,
Modélisation Cellulaire et Imagerie Biologique (EE1),
IFR 83, Bat B 7ème étage, porte 723, Campus Jussieu.
Tel : 01 44 27 46 92 Fax : 01 44 27 22 91
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