Very helpful and clear tutorial, really appreciate it

I can't thank you enough! You made my day! 🙏🏻🙏🏻🙏🏻

👌👌👌👌👌

Mandatory viewing for using the tool, thank you!

Great presentation

in the enter gene list can we provide the id of our circular rna?

Awesome

In the first step, do you mean about id the accession number or another id ?

It was a great tutorial. It would be nice if you could expand on the meaning of each part and their function in another video. For example, maybe explain how the acquired data can be used in research (or at least provide resources for beginners to follow and learn more). Also, if there are technical or specific types of plots that can visualize the results taken from DAVID, it would be very nice if you can cover them as well.

what is the alternative for Drosophila?

Thankyou

Your explantions are very clear, I enjoyed your videos and learned a lot. Thank you very much!!!

Very clear and specific ¡¡thanks

Fabulous! I haven't paid attention to epigenetic advancements in a decade or more, and am amazed at how much more has been discovered. The complexity blows me away!!

So how to use this software to do GSEA based on a specific subset genes or a defined subset genes by ourselves?

This was very helpful thanks!

What means enrichment?

I'm going to have to watch the Prime editing part 10 times more to understand it. It's simple yet complicated.

thank you

Hi, thanks for the tutorial. I had some trouble downloading the GSEA software so I ended up using the GenePattern UI. Is there any downside to using this website instead of the GSEA desktop application? Thanks

Really nice and useful video. Thank you.

So much help. Thank you.

Thank you so much for this tutorial! I'm new to proteomics and this video helped me a lot to get started on my data analysis

great

Thanks! Beatifull lecture. Really sad that you stopped making videos

thanks god, someone finally made all these clear. great job.

better explanation than my prof. who only says useless nonsense during the lectures.

Thank you! It is very well explained complext topic

This is GOLD! I am a biologist who does not know anything about bioinformatics, i've done a differential expression analysis of genes using RStudio and then i was like, what now, what to do with these DEGs? And then i found this amazing tutorial! THANK YOU! <3

Superb concept So much Thank

Very useful, thank you!

A great help. Thankyou mam

Thank you very much for the video! It helps! I have my functional annotation chart of GO TERM, now how could I export it to excel?

This video is amazing, so far my favorite. Really clear and straightforward, I truly appreciate it! Great job! many thanks :)

Very helpful - I have dabbled with DAVID from occasionally but this is the first time I really understood how to move beyond the initial set of results it gives.

Excellent talk Katherine

Lovely ❤thanks for the great lecture

Excellent! I finally understand it. However, one question: at 3:40 where the TALENs are biding to the DNA, it seems that the TALENs are too bulky to fit close enough together to bind to successive nucleotides.

Great

Thank you for this video I have a problem: GSEA don't run with download files from GSEA with .gmt format. I want to use the gene sets that I selected. Can anybody help me? Thank you so much

I have a wish 🙏 god, please let her return to youtube to make her awesome videos 🙏 Amen 🙏 Love from Turkey My Teacher 🙏

5:00 histone

Is this channel aims scientists

Super helpful and clear tutorial! I appreciate you saved me a lot time to figure out how to do such analysis!

Extremely helpful. Thank you very much.

Thank you

Thank you

Thank you so much. You have explained it in a simple and understanding way. I rate 5/5.

Thanks for the great resources you made. Very helpful :-).

Thank you for the video. How does one screen for mutations cause by off-target cutting of Cas9?