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extra:faqs [2020/01/31 16:52] – [Can I process tiled images?] pseudomoaner | extra:faqs [2020/07/01 12:31] (current) – [FAST feels very restrictive. Can I increase its flexibility?] pseudomoaner | ||
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===== FAQs ===== | ===== FAQs ===== | ||
+ | |||
+ | ==== FAST feels very restrictive. Can I increase its flexibility? | ||
+ | |||
+ | Much of FAST has been designed to limit user interaction with the GUI when this could cause data processing issues. These design choices include: | ||
+ | * The inability to open more than one module at once. | ||
+ | * The inability to interact with a module' | ||
+ | * The inability to access later modules before earlier processing stages have been completed. | ||
+ | Nevertheless, | ||
+ | |||
+ | <code matlab> | ||
+ | debugSet = false; | ||
+ | </ | ||
+ | |||
+ | to | ||
+ | |||
+ | <code matlab> | ||
+ | debugSet = true; | ||
+ | </ | ||
+ | |||
+ | **Note that data and program stability is not guaranteed if this change is made. You apply it at your own peril!** | ||
==== Can I process tiled images? ==== | ==== Can I process tiled images? ==== | ||
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Image cytometry is a simple alternative to flow cytometry, where microscopy is used to assess the fluorescence and morphological properties of thousands of cells simultaneously. After the appropriate experimental preparations, | Image cytometry is a simple alternative to flow cytometry, where microscopy is used to assess the fluorescence and morphological properties of thousands of cells simultaneously. After the appropriate experimental preparations, | ||
- | To use FAST to analyse image cytometry data, simply save each image in its own folder as described in the [[setup: | + | To use FAST to analyse image cytometry data, simply save each image in its own folder as described in the [[setup: |