Hi... Lisa ..when I opened this video I was hoping to get instructions to build a phyoT using different fungal DNA sequences with Mega...but this tutorial was also helpful...nicely explained the way DNA sequencer works
@isharajwade46105 ай бұрын
Fantastic video. Very well explained.. Thanks Lisa! 👏🤩
@simonpender83316 жыл бұрын
Love it - "drink milk, read books" - great advice.
@kamdynjaxon84793 жыл бұрын
you prolly dont care but if you guys are bored like me during the covid times you can watch pretty much all the new movies on Instaflixxer. Been streaming with my girlfriend these days =)
@jerrymekhi66473 жыл бұрын
@Kamdyn Jaxon definitely, I have been using instaflixxer for since december myself :D
@nguyenhuynhnga46353 жыл бұрын
Thank you so much.
@user-vh4pt1ws2w7 жыл бұрын
Very useful. Clear instruction!
@bidwansekhar7 ай бұрын
❤
@monalizapumihic95382 жыл бұрын
Thank you so much💗
@nohataha6398 Жыл бұрын
what if when using blast for unknown it gives 75 similarity identity?
@collaniedog66927 жыл бұрын
this is what I want. Thank you for this video.
@Azrael9284 жыл бұрын
Nice video, but could you teach how I can change or delete letter in an abi or scf file?
@fasdz55336 жыл бұрын
If i had a point mutation in my DNA sequence, can i determine wether it is nonesense or frameshift by analysing sequence data?
@armwanniwat93695 жыл бұрын
thank you so much
@hba38205 жыл бұрын
This is so helpful, thanks a lot!!
@yokaisamaful4 жыл бұрын
What if i get several alignements with 100% Query cover and 100% Per Ident after blasting my sequence in NCBI? what does it mean?
@Bigtigerfanmom4 жыл бұрын
Could you rephrase your question, please? I am unsure of what you're asking.
@ashabhardwaj19206 жыл бұрын
Hi. What should be the percentage of identity so that we could 100% sure about particular species and how do we know about new species?
@Bigtigerfanmom6 жыл бұрын
I checked with Dr. Chris Hittinger of UW Madison's Genetics - Hittinger Lab. This is his response: I agree you can’t be 100% sure without a 100% match. If it’s not a 100% match, it could be a sequencing error (which could be checked by looking at read quality or redoing it), or it could be natural variation within the species (very common). For it to be considered a new species, several criteria would need to be met. If it were substantially different (
@nemo93963 жыл бұрын
How do you identify a gene out of a sequence?
@Bigtigerfanmom3 жыл бұрын
Look for patterns. Something looks amiss visually.
@aqili.n50756 жыл бұрын
please where can i find this data (yHKS1.ab1) thanks
@amalienaahmad63536 жыл бұрын
hi. how to read the blast result? I mean, how i know if we discovered a new species from blast? based on your video, if the species already found, then the result shown the report mentioned that it have been sent by someone...but how the blast result show and report if it is new discovered? i just dont understand how to read it. do you have any tutorial on using blast? thank you.
@Bigtigerfanmom6 жыл бұрын
Hi! Good question! Once you've 'blasted' the results, if there is no close "hit", YOU may be on to a new discovery. How cool would that be? Name the organism after me - ha ha!
@prestonmartin82685 жыл бұрын
Interesting. I came a little bit
@Abyie-Ho-dam6 жыл бұрын
evolution? You people who study this think all this is random? mwahahahahahahahah