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Need to gather info about where the exports from the Flow Cytometer are being saved to, how we can get programmatic access to them.
Key takeaway from visiting the flow cytometer is how not-core the imaging data is to the analytical approach in the lab
Images are secondary, used to support conclusions but not to draw them
Images of single small entities are not intrinsically useful, it's how they group together that tells you about their classification and action
On-device analysis does clustering on other properties and that's (probably) what we see in the .fcs output files, in aggregate rather than linked to specific samples
The text was updated successfully, but these errors were encountered:
metazool
changed the title
Flow cytometer non-optical data
Flow cytometer data transfer
Jan 15, 2025
Need to gather info about where the exports from the Flow Cytometer are being saved to, how we can get programmatic access to them.
Key takeaway from visiting the flow cytometer is how not-core the imaging data is to the analytical approach in the lab
.fcs
output files, in aggregate rather than linked to specific samplesThe text was updated successfully, but these errors were encountered: