great introduction on icy

Brilliant.brilliant.brilliant!!! You could easily get more people watching with Promo-SM!!

Thank you very much ! Just started working with napari and this helped a lot !

Thank for your great video.

Thank you very much. I have watched a lot of Imagej tutorials on KZbin and your lecture was one of the best. You break down the steps of workflow very nicely. I really appreciate you sharing this recording.

thank u so much.

Thank dude! And good name for your hard drive hahaha, Greetings from Mother puncher!

really helpful! Thank you so much!

Very clear presentation and tutorial! Thanks!

wonderful! Thanks a lot! I Love it.

This is great! Thanks so much

Thank you very much. Excellent video.

Excellent overview, very helpful.

Excellent. Thank you guys!

Many thanks for sharing this video!

Great and intelligible course. I will recommend the video for my colleagues. All the best!

Thanks a lot for the great videos, I was struggling a lot starting data science with Python but these videos and github contents made everything easier. I have an issue though, when plotting data, I receive an error which is apparently an issue between numpy and python itself but I won't be able to plot my data and just returns a flat line, anyone might have an idea why that is?

Many thanks for the great presentation

thank you very much

Nice work! Motivating!

This was a great video!! Thanks you!

Thank you for the lecture. It's very helpful!

Thank you very much! This software is a legend.

58:58 BIOimage processing

for i in range(1,366): print("Thanks you very much")

This was gold! Thank you!

Very useful! Thank you so much.

How do you get your editor so beautiful, my editor looks very basic

Thank you very much!

Hello, is there a way for the end-user to know what magnification they are at? For example, zooming to a certain point shows you going form 4x to 10x or from 10x to 40x....

Thank you NEUBIAS and Fabrice!

If you click on this link it will download the example data and the macros: github.com/ahklemm/ImageJMacro_Introduction/archive/master.zip

Really good video thanks. I wanted to ask is there a way to save the settings i used to analyse one image so that i can apply it to other images (Trackmate plugin in Image J). That will save a lot of time. Thank you

Very well explained. Thank you

AS T.I the rapper would say "BANKHEADDDDDDDDDD!!!" ........ what a legend

Very good lecture! Thank you NEUBIAS and Fabrice!

This was sooo helpful ! Thank you

Great explanation! I am going to start to implement it immediately in my image analysis practice, thank you a lot :)

Very useful plugin and a very nice presentation. Thank you!

thank you A LOT for this webinar ! I am very grateful to be able to follow them!

ty)))

I can't believe that this software is free and open for everyone to use! We paid over than 20k pound to buy Visiopharm a few years ago to analyze the digital pathology slides. I just downloaded QuPath and now ready to explore this software. I am looking forward to receiving more surprise from it! Thank you very much for sharing it, and thanks to Dr Peter Bankhead to create and explain QuPath!

Congratulations! Napari is such a useful tool. I am material scientist and it has helped me a lot with the visualization and so on.

Thank you so much for you help!!

This was well done and useful. Look forward to additional videos from Neubias

napari is great! Thank you Nicholas and the team!

Cool explanation 😍

The questions and answers of this webinar are addressed on the Image-Sc forum: forum.image.sc/t/neubias-academy-home-webinar-tracking-cells-and-organelles-with-trackmate-questions-answers/38100

Impressive demonstration! Thanks for sharing.

Very well explained and very useful, thank you so much. It would be even better if you include your final macro in the comment section (it would be useful to check for mistakes when writing our own macros). Thanks again