Aafke Gros
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aafkegros.bsky.social
Aafke Gros
@aafkegros.bsky.social
Check out Microscopy Nodes for handling microscopy data in Blender! Now loading .tif and OME-Zarr with big volume support :)
she/her | IPA: ˈafkə ɡrɔs
I agree, is there a way to drop the name from the image mark (or maybe make multiple, one with the name big to the right of the logo?)
October 29, 2025 at 8:45 AM
Are you rendering all points as emitters? Or do they have some form of occlusion/absorption/scattering?
October 10, 2025 at 1:09 PM
Ah right, I have also seen some of the napari solution! I think this in general makes a lot of sense, and I'm still looking into how to make these kinds of volume interactions as easy in Blender as they are in the more scientific software, such as BigTrace and Napari 😅😋
September 24, 2025 at 12:23 PM
This is separate from Blender, built on imglib2 in java (same framework as bigDataViewer, so also related to bigWarp), and for bigtrace all implemented by @ekatrukha.bsky.social

I think the smart thing it does for annotation is to extract the brightest point under the mouse as targeted point
September 24, 2025 at 12:20 PM
This is the cool part of BigTrace, where this also has extensive semimanual and manual modes, while seeing your data in 3D. So this way, you can use the same engine to delete and fix traces.

Additionally i still want to make some automatic flags based on time info, but that will be more custom.
September 24, 2025 at 12:20 PM
I think it can be very useful to give a 'diorama' feel to a render and highlight certain complexity! But probably mostly for artistic purposes
August 27, 2025 at 5:00 PM
This is accompanied by a new set of tutorials showing exactly how you can start making beautiful microscopy visualizations in @blender.org!
Following along is also easy with the example OME-Zarr @openmicroscopy.org datasets 😄
Find the tutorials here: www.youtube.com/playlist?lis...
May 23, 2025 at 1:13 PM
Reposted by Aafke Gros
10 - Featured extension: Mastodon-Blender

Offers a bridge from Mastodon to Blender to create high quality 3D rendering of lineages and cell tracks over time:

(Tracking data of phallusia mammillata embryogenesis by Guignard et a. (2020). doi.org/10.1126/scie...)
January 30, 2025 at 4:44 PM
And it also works in 2D 😁 Here we extract a circular projection instead of a spherical, and apply a 1D Fourier transform.
Here we can see how the channel distributions all align in the projection after we optically activate Rac1 in one part of the cell. 💡
With @jpassmore.bsky.social , Lukas Kapitein
January 30, 2025 at 10:11 AM