Відео

You can peel a piece of callous skin and throw it in. They'd eat it too. Planarias are very fascinating worms.

You are from where

Do more feeding videos!

Thanks very good tutirial

Great guide, this has helped me with a class project. top work

My GOAT

once you download the program what do I need to open to get your starting screen in ImageJ?

Thanks, I would like to know how to present error bars in line graphs so that each error bar stands out and does not overlap

this helped me so much with my 12th grade research paper thank u!!!

Amazing, thank you for your enlightfully video. I guess we can use this method for evaluating dead/live biofilm formation. For instance, when I click "Invert LUT", green area change from green to red. I dont know if i use invert. Have u any opinion or advice?

Fantastic 👍

This video saved my International Baccalaureate Extended Essay. Appreciate it ;)

oh my god??? You're freaking amazing! LOVE IT!

Thank you for your video. I am following your video step by step but when I get to the thresholding point my background becomes red as well as the colonies. My colonies have been stained with crystal violet. So when I try to use the watershed function to separate out colonies the lines go through the background creating a grid rather than splitting up the colonies if that makes sense. Can you suggest why this may be?

Thanks

this video saved my life

Exactly what I needed!! Thank you.

Can you speak to how safe opening this application is? Scary to think about corrupting my laptop

Pretty cool - counting colonies are frustrating enough!! This made things so much easier - I hopes this works!!

Cool, Thanks. Trying to grow Streptococcus mutan. but it dosnt seem to stick to soy.

Thank you very much for the tutorial. Can you make a tutorial on how to measure the length and diameter (for example: tree root) of many images at once?

Thanks 🙏

Thank you

Thank you ! It helped me a lot, would love to see few more imagej application videos like this 😊👍

Great video, helped me a lot!

Holy crap! this is awesome, thank you so much for the tutorial!

Thank you for showing us how to this!! Saved our research!! Salute to you, Sir!

Excellent tutorial! I really appreciate how you used a very challenging image, completed an analysis that was less than optimal, and then walked through how to make it more accurate. I am sharing this with the college and grad students, and technicians in my lab at Emory.

thank you

congrats great video kai :)

helped a gal out in dire need! Thanks so much!

Hello Mr. Kai thanks for the video. It is very informative. I have 1Q: After you identify each cluster, e.g. when you reach the point of video time frame 10:50, can you then isolate each cluster so as to count the cells within each cluster e.g. using the analyze particle command?

I cannot thank you enough for this video!! I've been tearing my hair out for several days trying to figure out these precise tasks in ImageJ .... using their manual.... using trial and error .... etc. You solved all my problems in 15 short minutes. Nicely done job... I hope you are on your way to a great scientific career. I need to tell you that I am PhD scientist who's worked with video image analysis for 30 years. I am also a graduate of Hewlett High .... I assume you are in Lynbrook, LI ? I'm in central Oregon now... and wish you and the Lynbrook Science Program all the best!!

Thank you!!!

Excellent video. Very useful.

I have a doubt. Why did you not subtract the background in excel? Though you said in the video that you need to subtract the area by the background -- in the excel analysis, you did not perform the same....

Amazing video. It is very kind of you to teach all of us. You are amazingly clear

Good Video - Thanks

very good

Great job, thanks!

where's part 2 btw? :)

Life saver! OMG Thank you :)

Interesting, I've never seen this method before. Thank you!

Nice lecture! Congratulations, a simple but complete colony counting explanation with ImageJ.

Excellent video! I have a doubt. I want to supress a part of the image in the middle so I can analyze particle then. I have the feeling that everything ive tried doesnt work. Do you think you can help me. Maybe by email or from here?

Great video. Thank you. Quick question. Could this be applied to counting algal cells expelled during thermal stress experiments? Il have multiple pictures over periods of time and id like to analyse the differences in symbionts expulsions between them over time. Thanks again.

Hi, what kind of medium did you used?

Thanks a lot bro!)