http://confocal-microscopy-list.275.s1.nabble.com/akoya-file-format-tp7591754p7591762.html
using inForm first. You can merge component images using something like
QuPath. On a side note: QuPath works very well with qptiff files, it uses
bio-formats to read qptiff files. It should also be possible to write a
> *****
> To join, leave or search the confocal microscopy listserv, go to:
>
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>
> Simon,
>
> Bio-Formats Command Line Tools supports converting qptiff to ome.tiff,
> bio-fromats seems to carryover metadata (channel names and spatial
> resolution) nicely.
>
> A simple command like this should work:
> bfconvert input.qptiff output.ome.tiff
>
> There other flags you can pass while converting depending on your
> requirements, such as:
> -noflat -bigtiff -tilex 512 -tiley 512 -compression LZW
> -pyramid-resolutions 4 -pyramid-scale 2
>
> If the channels in your qptiff have cross talks and plenty of auto
> fluorescence then it might be better to unmix them in to component data
> using inForm first. You can merge component images using something like
> QuPath. On a side note: QuPath works very well with qptiff files, it uses
> bio-formats to read qptiff files. It should also be possible to write a
> script in QuPath to batch convert files.
>
> I have found Image.sc<
https://forum.image.sc/search?q=bfconvert> forums
> to be very resourceful for discussions related to ome.tiff conversion and
> QuPath<
https://qupath.github.io/>.
>
> Best,
> Ajay Zalavadia, Ph.D.
> Imaging Specialist, Imaging Core | Lerner Research Institute
> 9500 Euclid Avenue NB10 | Cleveland, OH 44195
> Phone: 216-444-8045 | email:
[hidden email]<mailto:
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>
>
> From: Confocal Microscopy List [mailto:
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> On Behalf Of Watkins, Simon C
> Sent: Friday, January 22, 2021 7:57 AM
> To:
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> Subject: [EXT] akoya file format
>
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> *****
> To join, leave or search the confocal microscopy listserv, go to:
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>
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy>
> Post images on
http://www.imgur.com<
http://www.imgur.com> and include the
> link in your posting.
> *****
>
> Colleagues, has anyone developed or have a solution for porting data sets
> from the Akoya platform (specifically the Vectra in our case) to an OME
> TIFF?
> We have been given the option or rescanning a ton of slides on one of our
> systems or finding a way to convert previously scanned data
> Thanks for the wisdom and of course stay safe!
> S
>
> Simon C. Watkins Ph.D
> Distinguished Professor and Vice Chair Cell Biology
> Professor Immunology
> Director Center for Biologic Imaging
> University of Pittsburgh
> Bsts 225 3550 terrace st
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