NCBI Minute: A Beginner's Guide to Genes and Sequences at NCBI

[@samuelnyandwi3349]

Thank you so much! I was absolutely lost for a bioinformatics assignment, and this video truly made me more confident!

[@morganreese7]

Yessss! Same here this helped tremendously for my presentation today!

[@anndiamond7601]

Thank you very much for detailed explanation, very helpful !

[@dukherdohonekorunrodone6346]

it'd be helpful if you could use your mouse pointer to show what part of the slide you are focusing on.

[@teshalesilas5442]

THAT IS GREAT CHANNEL

[@sabharabaya9838]

Thank for the video I have a question about Refseq When I search for a gene in the gene database I find that the number of exons in that gene is a specific number but when I go to the RefSeq of that gene I find that the number of exons is different, can anyone explain that for me

[@stanleynonso3715]

Hi, thank you for this video, I am working on genes associated with schistosomiasis and its resistance, how do I go about it and How do I have your videos that will guide me through

[@ibrahimssali7360]

VERY GOOD LECTURE

[@ayudashintastri1952]

Thank you very much Sir for your good video

[@ongerijustineonderi2208]

Hey friend, how can I get to see the hits of nucleotide BRCA2, I don't know how to check hits

[@LatterDayYouth]

I followed through this lecture in Aug. 2020 and cannot find E. coli that appears in the video at 24:11. It doesn't matter to me if E. coli is in the list of blast against human APRT (not the protein of my interest), but I wonder what made this difference in the query results. Is it updates in E. coli DB? I'd like to know why it happened in order to fully understand the NCBI platform.

[@LatterDayYouth]

One more question. The active site annotation doesn't come up when I click on the 'Functional sites' annotations unlike the video, 25:55 . Could you help me?

[@samuelmason6427]

Gene structuring or enhancement

[@hasanashfaq3853]

I have question sir, if I want to characterize a gene on molecular basis, but the gene, I am searching for appear to pop up containing different variants starting with i.e. XP, but no NP sequence, which sequence should I use to design primers, please answer.

[@13inas]

Great! thank you

[@Forza-nz7sh]

Sir Francis Crick called that...

[@khatysimamora8683]

ga ngerti

[@bencemolnar8705]

This tutorial is quite bad... The quality of sound and the process, it's like: it is science! It should be only complicated and very scientific!!! (I get the mechanism of this part of databases although the tutorials for this topic are horrible, especially from NIH itself.) There should be more practical stuff and less "just sciencitific X,Y,Z search", I think.