The general process for detecting regions of interest (ROI's) is:
Threshold or Edge Detection -> Binarize -> Watershed/Fill/Etc -> Particle Analysis -> Measure
I personally think that this site has a good tutorial that gives you thorough examples without getting bogged down in detail:
http://www.macbiophotonics.ca/imagej/Here's an e-mail that contains websites with more detailed documentation that I sent one of my co-workers who was interested in imageJ:
"Here is the official webpage for the original imageJ software documentation:
http://rsbweb.nih.gov/ij/docs/index.htmlHere is a direct link to the important stuff. These are the "tools"
that I was talking about:
http://rsbweb.nih.gov/ij/docs/macro_reference_guide.pdfHere is another direct link to more important stuff. This explains
functions, for loops, and other general programming concepts:
http://rsbweb.nih.gov/ij/developer/macro/macros.htmlHere is another "flavor" of imageJ. There is additional documentation
that you can use from this site:
http://www.macbiophotonics.ca/imagej/Here is another "flavor" of imageJ. There is also additional
documentation that you can use from this site:
http://pacific.mpi-cbg.de/wiki/index.php/Fiji"