-
## Analysis Goal (What should be done / analysed?)
Segment the nuclei in this image using Voronoi-Otsu-Labeling. While loading the image, make sure to use the first channel only.
## Image Upload…
-
I would like to segment the first channel of this image using Voronoi-Otsu-Labeling.
g…
-
## Analysis Goal (What should be done / analysed?)
Write a notebook that creates a 500x500 pixel image showing nuclei. Use a Gaussian blur to simulate the PSF of a microscope. Put some noise on top…
-
## Analysis Goal (What should be done / analysed?)
I'd like to create a notebook for segmenting the image below. I _think_ a seeded watershed algorithm can do it. Unfortunately, I do not have seeds…
-
## Analysis Goal (What should be done / analysed?)
I would like to segment the nuclei in this image, e.g. using Voronoi-Otsu-Labeling.
## Image Upload
📎 **Drag & drop your microscopy image here…
-
What algorithms / Python packages would be suited for segmenting cells in this kind of microscopy image?
![membranes](https://github.com/user-attachments/assets/3b813c91-e001-4df0-84e2-3ca1045fdc1b…
-
BioImage.IO - a collaborative effort to bring AI models to the bioimaging community.
They have already defined a way of working to integrate different communities into the Zoo.
> Usually, a co…
-
Project Lead: Andrés Olivera
Mentor: Esther Plomp
Welcome to OLS-7! This issue will be used to track your project and progress during the program. Please use this checklist over the next f…
-
Hi,
The BioImage.IO team will meet every Wednesday 4PM CET, [check the next meeting in your time zone](https://arewemeetingyet.com/Stockholm/2022-07-13/16:00/w/BioImage.IO%20Weekly%20Meeting#eyJ1c…
oeway updated
16 hours ago
-
### 1. Description of your software, organization, company or team
SpotMAX is a Python software for the analysis of multi-dimensional fluorescence microscopy data.
- Preprint: https://www.biorx…