[ome-devel] Spectral Chemical Imaging Data
Munro, Ian
i.munro at imperial.ac.uk
Thu Jan 7 09:55:54 GMT 2016
Happy New Year to you as well Alan.
If you log in again now and change group to “Experimental Formats” you should hopefully be able to see some data under “Mass spec proof of concept/MouseCerebellum”.
If this file format were to be supported in OME the first step would be to write a Bio-Formats reader.
In order to give a flavour of what that might look like I have attempted to extract the data (N.B. not metadata) from your file and write it into OME-TIFF files for which a reader already exists.
The first file there “MouseCerebellumC" - I have mapped your data into the 5D OME data model with m/z as channels , which seemed to me most appropriate.
Unfortunately this image is not easy to view using the standard OMERO clients which, for historical reasons, interpret large numbers of channels as time.
From our earlier discussions, however it seemed likely that you would want a spectrum oriented view so in the second file “MouseCerebellumT” I’ve stored the data as if it were FLIM data with m/z mapped to time(t).
This will allow you examine the data using the FLIMfit tool http://downloads.openmicroscopy.org/flimfit/4.9.1/
Frustratingly, you cannot, I’m afraid, log on to the demo server directly from FLIMfit as a version compatible with OMERO 5.2 has not yet been released so it will be necessary to download the file as described in http://help.openmicroscopy.org/export.html#download and open locally.
N.B. you will need to change the background from the default value of 200 to 0.
The screenshot illustrates what I see when I do this.
Obviously I’m not suggesting that FLIMfit is appropriate for your data, but attempting to illustrate how it might look if you were to adapt your existing tools to be OMERO clients.
I hope all that makes sense.
Best Regards
Ian
[cid:4323764B-1BA7-45ED-A470-CD70A12261AC at home]
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