Hello ImageJers’
I have a set of z-stacks of adult Drosophila brains where some of the cells (neural stem cells and neurons) are GFP-positive. There is also a bit of GFP+ background. I want to segment and reconstruct a 3D model of the GFP+ cells only (obviously without the background). Then I want to count the cells and measure their volume. After fiddling around with binary masks, 3D ROI and 3D segmentation, I am still at a loss for a ‘standardised’ way. Can someone kindly suggest a plugin etc or a methodology to solve the problem? Thanks and Best FlyGuy *************************** With thanks and Best Wishes Fly Guy Twitter: @flyguy -- ImageJ mailing list: http://imagej.nih.gov/ij/list.html |
Hi.
You might want to check this article and what (and how) they have done. http://www.sciencedirect.com/science/article/pii/S2405471217300522 Though, as I know, there is still no easy and established way to do what you want. On Mon, Jul 3, 2017 at 1:25 PM, Fly Guy <[hidden email]> wrote: > Hello ImageJers’ > > I have a set of z-stacks of adult Drosophila brains where some of the > cells (neural stem cells and neurons) are GFP-positive. > There is also a bit of GFP+ background. > I want to segment and reconstruct a 3D model of the GFP+ cells only > (obviously without the background). Then I want to count the cells and > measure their volume. > After fiddling around with binary masks, 3D ROI and 3D segmentation, I am > still at a loss for a ‘standardised’ way. > > Can someone kindly suggest a plugin etc or a methodology to solve the > problem? > > Thanks and Best > FlyGuy > > > > > > > *************************** > With thanks and Best Wishes > Fly Guy > Twitter: @flyguy > > > > > > > -- > ImageJ mailing list: http://imagej.nih.gov/ij/list.html > -- Vasily A Popkov Lab.Structure and function of mitochondria A.N.Belozersky Institute of Physico-Chemical Biology Moscow State University -- ImageJ mailing list: http://imagej.nih.gov/ij/list.html |
In reply to this post by Fly Guy
Hi FlyGuy,
A seemingly straightforward task, but it can be quite cumbersome... I would suggest using the TrakEM2 plugin (included in FIJI). You can segment individual cells in separate AreaLists and get measurements afterwards. Perhaps the Segmentation Editor could also work. Good luck, Jitte On Mon, 3 Jul 2017 at 12:25 Fly Guy <[hidden email]> wrote: > Hello ImageJers’ > > I have a set of z-stacks of adult Drosophila brains where some of the > cells (neural stem cells and neurons) are GFP-positive. > There is also a bit of GFP+ background. > I want to segment and reconstruct a 3D model of the GFP+ cells only > (obviously without the background). Then I want to count the cells and > measure their volume. > After fiddling around with binary masks, 3D ROI and 3D segmentation, I am > still at a loss for a ‘standardised’ way. > > Can someone kindly suggest a plugin etc or a methodology to solve the > problem? > > Thanks and Best > FlyGuy > > > > > > > *************************** > With thanks and Best Wishes > Fly Guy > Twitter: @flyguy > > > > > > > -- > ImageJ mailing list: http://imagej.nih.gov/ij/list.html > -- ImageJ mailing list: http://imagej.nih.gov/ij/list.html |
In reply to this post by Fly Guy
Hi,
I recommend KNIME [1] to easily 3D-segment and count/measure objects. There are a few related discussions on the ImageJ forum: *** http://forum.imagej.net/t/segmentation-counting-cells-in-3d/2279?u=imagejan http://forum.imagej.net/t/knime-image-processing/91?u=imagejan http://forum.imagej.net/t/identify-nuclei-and-spots-in-imagej/94?u=imagejan *** Also have a look at the example workflows accessible from the Example Server within a KNIME installation. Cheers Jan [1]: http://knime.imagej.net/ On 03.07.2017 12:25, Fly Guy wrote: > Hello ImageJers’ > > I have a set of z-stacks of adult Drosophila brains where some of the cells (neural stem cells and neurons) are GFP-positive. > There is also a bit of GFP+ background. > I want to segment and reconstruct a 3D model of the GFP+ cells only (obviously without the background). Then I want to count the cells and measure their volume. > After fiddling around with binary masks, 3D ROI and 3D segmentation, I am still at a loss for a ‘standardised’ way. > > Can someone kindly suggest a plugin etc or a methodology to solve the problem? > > Thanks and Best > FlyGuy > > > > > > > *************************** > With thanks and Best Wishes > Fly Guy > Twitter: @flyguy > > > > > > > -- > ImageJ mailing list: http://imagej.nih.gov/ij/list.html > -- ImageJ mailing list: http://imagej.nih.gov/ij/list.html |
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