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May i ask, how exactly do you find these universal primers? Do we just type 16s in NCBI, then find the primer for that? Because usually, in NCBI, they're species specific, not umiversal

Awesome!

I am currently studying Wilson Disease, and based on the literature I have gathered, there is no well-established genotype-phenotype association. Also, there are multiple mutations across all 21 exons of the ATP7B gene. But most of the literature also state that they are using ACMG guidelines for classifying variants. Any comment on that?

Very good presentation. thanks for sharing.

Awesome, thanks a lot for this video

Thank you Iowa Institute for Human Genetics. Greetings from a bioeng grad student from Universidad del Cauca, Colombia.

Thank you very much for this wonderfully presented material.

Great video. Thank you!

I don't understand. If you want to detect what genes are off or on and by how much they are expressed then why not just use epigenomics instead of transcriptomics?

lache la traduction en français ta voix de cancéreux là

Best lecture on metagenomics, wish for further information 👌

Could you please share the link

Wish I could see this great video earlier. So many questions solved.

great webinar!

Is this just applied to gremlin variant? Can it be applied to somatic variant?

Thank you 10x team and the host. Can I get a copy of the slides to use for my rehearsals? I am trying to understand the work flow of single cell seq to use on my postgraduate project and this could be of great help. Again, thank you so much for the presentation.

Hello, awesome video. Could the .html be shared? thanks

Could you please give us access to the document used in the video?

I have chronic gut issues that comes along with all other kinds of side effects. Is there any way to get into this study as a patient? I have an appointment at Ohio state coming soon. My life is falling apart and most of my doctors don't seem to understand the severity of it.

This is such a helpful video. Thank you so much!

Could you please give link to access data shown in video

This was excellent -- are slides publicly available as implied at the end of the lecture?

thank you so much for the presentation! well explained!

thanks

Dr. Michael mentions at 48:17 that he did a webinar on pathway analysis. Could you please share the link? Thank you!

This video is a great summary of Metagenomics!

Thanks so much for the video. Very informative. Uts my first time to read about metagenomics because I have an interest for my PhD and your video motivates me. Thanks 😊

Thanks for the video. Please make a video on chip seq analysis in R starting with GEO dataset, there is no proper one on internet so far.

Nice video, thanks Michael! I'm a molecular biologist who struggles with the basics of bioinformatics so this really helped.

Thank you very much Dr. Kolbe this is a very useful and informative overview.

Thanks a lot. very well explained.

This is wonderful information about bioconductor and Public database!

thanks for sharing, greetings from Spain!

theng you...

This is really terrific, thank you so much for providing it to all. The 10X folks did a great job IMHO: very well organized and clear, many tips on how to succeed. Hoping to run my first 10X experiment very soon and this is very reassuring information to have at hand. Hopefully I can find a pdf of these presentations, but if not I'll just take screen captures. Cheers!

Informative and concise. Thanks!

Great video! Thank you!

Really appreciate this explanation, as I'm having my first go at writing a protocol for a job.

this is amazing helpful! wow thank you 10x !!

Great presentation! Systematic and very easy to follow, thanks for putting this together!

BA1 is benign-standalone not benign-automatic. Its weight is so heavy that just that criteria itself can cause the variant to be considered benign as the name implies.

Excellent!

Thanks. Very well-described

Great video! Cheers

Great! So explanatory. Thank you.

Thank you

thanks

Could you guys potentially consider copy-number variant discovery using NGS data? I work at a university and most of our research staff no about copy-numbers and the data you get back, but have no clue how this data is derived. The resources available are pretty high level!

Im an undegrad writing a thesis for my honors program. COVID destroyed my proposal and had to switch up to a remote RNAseq analysis - you've just saved my college career sir thank you