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Hi,
I'm using a Bio-rad confocal microscope to analyze fluoroscentlly-stained biofilms.
currently I set a treshold value, which above this value the imageJ counts the pixels and below this value it ignores it. However, I'm looking for a way to analyze all the images in a sequence individually, so I can track the pattern of the pixels density. So basically the output I'm looking for will contain the number of pixels for every image in the sequence. From these value I'll be able to draw a graph showing the change in pixels at various depths of the Biofilm.
Another question is how can I merge two image sequences?
Thank you all!
Lior Eshed
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" In wine there is wisdom, in beer there is strength.
In water there is bacteria "
- German proverb
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