[chimerax-users] segmented tomogram density in chimeraX

[Tom Goddard]

Hi Jesse,

  I guess your segmentation has assigned an integer region number to each grid point.  It sounds like those region numbers range from 240 to 250.  Displaying that as if is a density map with contour surfaces isn't very useful as you point out.  Instead you can use the ChimeraX segmentation command to make a surface for each region, for example

	segmentation surface #1 each segment

where "#1" is the id of the segmentation model you opened, and the "each segment" part says to make a separate surface for each region instead of one surface that includes all regions,  Documentation is here

	https://www.cgl.ucsf.edu/chimerax/docs/user/commands/segmentation.html <https://www.cgl.ucsf.edu/chimerax/docs/user/commands/segmentation.html>

You can also color your tomogram using the segmented regions using the "segmentation color" command.  There are examples of both commands for segmented neurons in a rat brain here

	https://www.rbvi.ucsf.edu/chimerax/data/layer4-june2020/mousebrain.html <https://www.rbvi.ucsf.edu/chimerax/data/layer4-june2020/mousebrain.html>

This example is a bit fancier than your data in that multiple attributes are associated with each region of the segmentation.

	Tom



> On Oct 24, 2022, at 6:46 AM, Jesse HANSEN via ChimeraX-users <chimerax-users at cgl.ucsf.edu> wrote:
> 
> hi all,
> 
> I have segmented a tomogram in Amira and exported to chimera for visualization. I first opened the .rec file in chimera and re-saved as .mrc.  Okay, the segmentation output gives a fully filled volume cube except for the regions of segmentation.   Obviously things are inverted.  Also, the volume viewer shows clear sharp peaks (delta functions) rather than continuous density, as volume slider moves to the right new segmentation features appear.  So I used volume filter with "scale" to -1, and I turned off "displayed subregions only".  This fixed the inversion problem and now as I slide toward the right I see more segmented densities.  However the threshold values are all negative (-250 on the far left to -240 on the far right).   This, combined with the densities being sharp peaks, makes it impossible to use this volume like a regular volume for surface coloring, filtering, segger, etc.  Any suggestion on how to go from this step to a usable density would be appreciated.
> 
> thanks!
> Jesse
> =================================
> Dr. Jesse Hansen
> Schur Group
> Institute of Science and Technology Austria
> Am Campus 1
> 3400 Klosterneuburg
> Austria
> _______________________________________________
> ChimeraX-users mailing list
> ChimeraX-users at cgl.ucsf.edu <mailto:ChimeraX-users at cgl.ucsf.edu>
> Manage subscription:
> https://www.rbvi.ucsf.edu/mailman/listinfo/chimerax-users <https://www.rbvi.ucsf.edu/mailman/listinfo/chimerax-users>
-------------- next part --------------
An HTML attachment was scrubbed...
URL: <http://www.rbvi.ucsf.edu/pipermail/chimerax-users/attachments/20221024/6c28f8b4/attachment-0001.html>
-------------- next part --------------
A non-text attachment was scrubbed...
Name: segmentation.jpg
Type: image/jpeg
Size: 849792 bytes
Desc: not available
URL: <http://www.rbvi.ucsf.edu/pipermail/chimerax-users/attachments/20221024/6c28f8b4/attachment-0001.jpg>