My seq results have 10 sequences that have almost 100% identity, 1 “gap,” and 0 “E-value.” Don’t know how to single out the best match; even trimmed the “N’s.”
i will submit coi sequences for new species not submitted before in ncbi, please what kind of analysis i can includes in results in article (this my first experience in molecular tools , am not an expert) please help me , thank you
Wow what an amazing way to teach. I was in search of like this class of bioinformatics, now my thirst comes to end to find ur channel video. I am from India
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The important thing i have understod from this video
1. Max idenitities
2. Lowest E value
3.minmum gaps
Thank you! This was so much more helpful than the long lecture videos on some of their websites!
Wow, such an organized and informative video! I've just started some bioinformatics work in my lab and this was SO helpful. THANK YOU
I wish you went into more detail about every notation and what they mean.
Thanks for this information
How do you use BLAST to know that frameshift happened on your protein?
My seq results have 10 sequences that have almost 100% identity, 1 “gap,” and 0 “E-value.”
Don’t know how to single out the best match; even trimmed the “N’s.”
Great work
What playlist is this in on your channel? I want to check out more related videos!
thank you so much !!!
i will submit coi sequences for new species not submitted before in ncbi, please what kind of analysis i can includes in results in article (this my first experience in molecular tools , am not an expert) please help me , thank you
when using blast for unknown it gives 75 similarity in identity?? What is that mean??
How can you know if there is any mutation in the sequence you provided?
Wow what an amazing way to teach. I was in search of like this class of bioinformatics, now my thirst comes to end to find ur channel video.
I am from India
Thanks !
Hi, thanks for the video. it would be very useful a tutorial for blast all against all option. Thanks!
How can you interpret the PSSM Matrix which is generated after a PSI-BLAST?
Amazing
Hello, if i have the nucléotides and i cherche the protéine,how??
liked your video sir,
would you plz tell how to do blastX in NCBI for long contigs (In Million bp size)
I want From you make lecture about how use MOLE BLAST
Why so many Ns occur in the results?
Select a gene of interest and do BLAST search, and describe results in details. Give me this solution noww
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Guys how to search homologue