Thanks to everyone who attended my first course on image processing (and acquisition as it turns out). As promised here are some links:
- MBF Tools for ImageJ. This is a suite of processing and analysis tools, provided by the McMaster Biophotonics Facility, which can be used for, among other things, splitting apart pigment based IHC [...]
If you want to merge multiple channels in Elements here is a quick solution:
1. Make sure you have the channel tabs activated. Do this by clicking the Edit menu, then Options. Select the “Appearance” settings. Make sure the “Show Channel Tabs” box is checked.
2. open or acquire the first image. In the lower left corner [...]
If there is one simple question I get during training sessions it’s “How do I save an image, so that I can open it using Photoshop or other programs, and have the image appear exactly as it does in Elements?”. The reasons for this are complicated. Suffice it to say if all you want is [...]
If you are enrolled for the Bio-X Image Processing and Analysis Workshop, I want to make sure you get the most from the course. To that end:
If you don’t have a laptop please find someone to work with during the course, so you can follow along. Most of the subject matter is better absorbed if [...]
When using the “Wellplate2″ Macro with NIS AR you may have noticed a small but important limitation: Once you’ve loaded your specified sites into the 6D experiment, you can no longer make adjustments to the scope PFS offset. This means that for each experiment you run you either need the offset to stay the same, [...]