This workflow is designed to batch import Bruker files into ImageJ formats. It also imports the frame rate and pixel size, assuming the correct objective is set.
As of version 230229, this workflow is working for files saved on the SFC and confocal systems. Please note the following limitations:
- This workflow is designed for timeseries data and may not work with single z-stack images.
- The MIP (Maximum Intensity Projection) image should be saved already from the microscope.
- While this workflow should work with any number of channels, it has only been tested with 2-3 channels.
To use this workflow, follow these steps:
- Open the
main_workflow.py
file. - Use the GUI to select the parent folder containing the Bruker folders for individual movies. 2a. Alternatively, you click comment out the gui code and just copy and paste the path to the folder in the correct location.
- Run the
main_workflow.py
script.