Hello Matt,
> I'm current working on our software to write OME-TIFFs and wanted to know where the best place to store the following:
Always great to hear from people writing to our file format.
> - Scan rate (Fps) of the confocal
We do not have a location to directly store a scan rate.
We have a TimeIncrement on Pixels:
http://www.openmicroscopy.org/Schemas/D ... tml#PixelsWe also have a value DeltaT to store the time at acquisition of each Plane
http://www.openmicroscopy.org/Schemas/D ... html#Plane> - Wavelength (nm) of the laser
http://www.openmicroscopy.org/Schemas/D ... html#Laser> - Channel power (%) of the laser
The constant power of the laser in milliwatts[mW] can be store in LightSource
http://www.openmicroscopy.org/Schemas/D ... ightSourceIf you want to vary the percentage with channel then you need to use a LightSourceSettings object in each channel. This has Attenuation %:
http://www.openmicroscopy.org/Schemas/D ... ceSettings> - Dichroic & Barrier filter
The filter system is described in the docs here:
http://www.openmicroscopy.org/site/supp ... erset.htmlYour barrier filter would map to the models Emission filter.
You probably want to define a LightPath and populate it:
http://www.openmicroscopy.org/Schemas/D ... #LightPath> Also I have ran the OME validator with some test images and it came out with no errors. However when I try to load it into JImage, it returns errors when attempting to read the meta-data.
The validator can only check the structure of the file and internal references. It does not validate the values stored in the metadata other than checking they are the correct type.
> Edit: Is there any other way of checking the validity of our OME structure or is it just through the OME.qa website?
All the QA website does is submit files. I have been validation them manually. As there was no email address attached to the files I had no way to reply. This may we a bug with the QA system, we are checking. I have added comments to the different files sets I think you have submitted, links to them are below:
http://qa.openmicroscopy.org.uk/qa/feed ... b6c18254bbhttp://qa.openmicroscopy.org.uk/qa/feed ... f7ea33f1e3http://qa.openmicroscopy.org.uk/qa/feed ... 46977062ceI was using the xmlvalid command, part of the bioformat command line tools:
http://www.openmicroscopy.org/site/supp ... t=xmlvalidIt can also process OME-TIFF files, e.g. xmlvalid myfile.ome.tiff
Another useful command is showinf, this performs a test read of a file using bio-formats.
Oh, if you are going to be writing Florsence Lifetime data check out:
http://www.openmicroscopy.org/site/supp ... orage.htmland our first solution using these structures:
http://www.openmicroscopy.org/site/prod ... er/flimfitHope this helps,
Andrew