We are currently testing OMERO as a microscopy database solution for our institute. All of the microscopes will be from Leica and Leica is using the lif-file.
We imported several lif-files from confocal systems with different content, like normal images, z-stacks, time-series, tiled images.
In all cases the meta-data for the used excitation wavelengths show wrong values in the OMERO insight client. Additionally we also checked the meta-data in ImageJ and also there the the shown excitation wavelengths were wrong.
We are using LAS AF 2.4.1 (build 6384) on a SP5 and LAS AF 2.5.1.6757 on the LSI.
For OMERO, we have installed our own server (version 4.3), which seems to be running fine in all other aspects.
In the attached image, you can see a screenshot of OMERO Insight and the shown meta data, in red the wrong shown data, in blue the data which were right. In all experiments the same sample was used:
DAPI, blue, cell nucleus (excitation with laser 405)
Alexa488, green, phalloidin (actin) (excitation with laser 488)
Mitotracker, red (excitation with laser 561)
Has anyone encountered this problem before? Could it be an issue with the Leica file format or LOCI ?
Thanks,
Joern