Hey Friends, todays topic will be: Bisulfite Sequencing, which is a method for the detection of DNA Methylation. Hope you enjoy it. Cheers, Henrik
Жүктеу.....
Пікірлер: 54
@henrikslab8 ай бұрын
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@saleemamehboob754910 ай бұрын
Great explanation. Very comprehensive summary with good animation👍👍👍
@TheSummerOf864 жыл бұрын
Great video, short and simple, nice graphics. Thank you!
@xXArtimixXx2 жыл бұрын
Beautifully and quickly explained. Thanks for the video, you earned a sub!
@nanashalev76122 жыл бұрын
Amazing explanation, right on the point. Thanks :)
@cankale80022 жыл бұрын
I really like these kinds of videos where you understand every part of the topic. It was really helpfull.
@NickoReese2 ай бұрын
Great video! Thank you for explaining it so fully.
@elanafarrell59292 жыл бұрын
This is super informative and easy to understand thank you
@aamaramuzaffar35652 ай бұрын
You way of teaching is amazing
@quinattasneemrafique536 Жыл бұрын
Amazing crisp explanation. Thanks a lot
@orxanibayev3402 жыл бұрын
Helped a lot, many thanks!
@nivethanimmy9985 Жыл бұрын
Explanation was clear. thank you.
@mariociencia122 жыл бұрын
I just donated about 2 dollars for the video. But the video deserve much more than that
@Mohannad23801 Жыл бұрын
This was very useful thanks a lot!
@bartkuk13 ай бұрын
Very clear explanation. Thank you 😊
@ebtihal19907 ай бұрын
Great explanation, thank you for your help
@genicadelara52433 жыл бұрын
Thank u so much. This is helpful.
@Daisy-lg7sq10 ай бұрын
Thank you so much for clear explanation ❤
@Displ4c3 ай бұрын
Awesome 🙏🏻 thank you
@curioussepia7677 Жыл бұрын
Thank you ,it was helpful.
@navyanandhanaofficial Жыл бұрын
Very nice video thanks for sharing
@nabyl7404 жыл бұрын
Nice channel and nice videos 👌
@naifalharbi6730 Жыл бұрын
Amaaaaaazing thank u
@hadijohni232 жыл бұрын
so grateful sir
@bhavikatiwari27462 жыл бұрын
Thanks for this easy explanation!
@henrikslab
2 жыл бұрын
Thanks for watching!
@younesabuelayyan4520 Жыл бұрын
well explained, thanks.
@NK1887214 күн бұрын
Very helpful.
@mdkhurshid75982 ай бұрын
Excellent
@c.wredacted25896 ай бұрын
Thank you so very much
@omercetin1683 Жыл бұрын
Good exp.
@mayconmarcao45542 жыл бұрын
Well done explanation! But I have to confess that the "arrows" you showed ( C > C or C > T) looks like "greater than". 3:34
@henrikslab
2 жыл бұрын
I agree! This is a bit misleading..
@yaxiu37993 жыл бұрын
Good.
@rougang_04714 жыл бұрын
I'm wondering how to confirm the specific T(which is the unmethylated cytosine) after PCR? And also thanks for your video which is clear and easy to understand!
@henrikslab
3 жыл бұрын
You wonder how distinguish between the “new“ T (unmethylated cytosine) and the “normal“ T in the DNA, correct? This works only by comparing the untreated DNA with bisulfite treated DNA... (sequencing) e.g. Untreated DNA A T C A G G Treated DNA A T T A G G the first T was originally also a T the second T was initially an unmethylated C
@dinushiarambegedara9906
2 жыл бұрын
@@henrikslab Do you know a way to compare the bisulfite converted sequence with a non-converted sequence? A software maybe?
@jinglin4358
9 ай бұрын
I know this question is a few years old but it’s possible to sequence whole genome with low concentrations of DNA ie extracted and not amplified DNA with next gen sequencing. So you can compare the sequence prior to bisulfite conversion and after.
@ashukhan-jr2kl4 жыл бұрын
My first like and first comment
@henrikslab
4 жыл бұрын
What an honor!
@sadafyasmeen31112 жыл бұрын
Well, how are we gonna use the same primers for the template whose Cs are changed to Ts in PCR?
@mariociencia122 жыл бұрын
Valeu!
@henrikslab
2 жыл бұрын
Not again... stop it, Mario! Thank you, man!
@mariociencia122 жыл бұрын
The video is very nice. However, I had not understood at first glance why U is converted into T in PCR. In another video, I saw that a complementary sequence is generated in a first-round, where U is paired with A. Then, in a second-round, the primary sequence is generated, but with T paired with A. It is equivalent to the conversion of U into T. I had confused because, in the cell, the U in DNA appears to be corrected into C. If the video showed the conversion of U into T in PCR it will be perfect!
@henrikslab
2 жыл бұрын
I agree! I decided to skip the step you mentioned ´cause I put the focus on the bisulfite conversion itself. But you described it correctly! I said "certain rounds of PCR" to simplify everything, but U is paired with A and this newly synthesized strand is paired with T then! True
@alxdr94513 жыл бұрын
love for that still
@markrudolf75672 жыл бұрын
How do you know a given base was an un-methylated C and not a T? Do you to compare it the original sequence somehow?
@jinglin4358
9 ай бұрын
Yes. You compare post PCR sequence to pre. it’s possible to sequence whole genome with low concentrations of DNA ie extracted and not amplified DNA with next gen sequencing. So you can compare the sequence prior to bisulfite conversion and after.
@alerookoh87483 жыл бұрын
I thought methylation mostly occurs at CpG islands alone?
@henrikslab
3 жыл бұрын
A CpG island is a region in the DNA with a high C G dinucleotide frequency and density. They are often located in promoter regions. Indeed, here we find an important part of methylation. You probably talk about CpG *sites*? Mainly methylation occurs at CpG sites, true. However, there is also methylation at CpA, CpT and CpG sites. See -> www.ncbi.nlm.nih.gov/pmc/articles/PMC5485512/
Пікірлер: 54
[Affiliate Link/Anzeige] Hey there! If you're looking for NGS size selection and library prep beads that don't break your bank, my friends at Cambrian have a great product called CamSelect NGS. Use my code "HENRIKSLAB15" and get 15% off on any product along with free shipping! cambrianbioworksin.myshopify.com/discount/HENRIKSLAB15
Great explanation. Very comprehensive summary with good animation👍👍👍
Great video, short and simple, nice graphics. Thank you!
Beautifully and quickly explained. Thanks for the video, you earned a sub!
Amazing explanation, right on the point. Thanks :)
I really like these kinds of videos where you understand every part of the topic. It was really helpfull.
Great video! Thank you for explaining it so fully.
This is super informative and easy to understand thank you
You way of teaching is amazing
Amazing crisp explanation. Thanks a lot
Helped a lot, many thanks!
Explanation was clear. thank you.
I just donated about 2 dollars for the video. But the video deserve much more than that
This was very useful thanks a lot!
Very clear explanation. Thank you 😊
Great explanation, thank you for your help
Thank u so much. This is helpful.
Thank you so much for clear explanation ❤
Awesome 🙏🏻 thank you
Thank you ,it was helpful.
Very nice video thanks for sharing
Nice channel and nice videos 👌
Amaaaaaazing thank u
so grateful sir
Thanks for this easy explanation!
@henrikslab
2 жыл бұрын
Thanks for watching!
well explained, thanks.
Very helpful.
Excellent
Thank you so very much
Good exp.
Well done explanation! But I have to confess that the "arrows" you showed ( C > C or C > T) looks like "greater than". 3:34
@henrikslab
2 жыл бұрын
I agree! This is a bit misleading..
Good.
I'm wondering how to confirm the specific T(which is the unmethylated cytosine) after PCR? And also thanks for your video which is clear and easy to understand!
@henrikslab
3 жыл бұрын
You wonder how distinguish between the “new“ T (unmethylated cytosine) and the “normal“ T in the DNA, correct? This works only by comparing the untreated DNA with bisulfite treated DNA... (sequencing) e.g. Untreated DNA A T C A G G Treated DNA A T T A G G the first T was originally also a T the second T was initially an unmethylated C
@dinushiarambegedara9906
2 жыл бұрын
@@henrikslab Do you know a way to compare the bisulfite converted sequence with a non-converted sequence? A software maybe?
@jinglin4358
9 ай бұрын
I know this question is a few years old but it’s possible to sequence whole genome with low concentrations of DNA ie extracted and not amplified DNA with next gen sequencing. So you can compare the sequence prior to bisulfite conversion and after.
My first like and first comment
@henrikslab
4 жыл бұрын
What an honor!
Well, how are we gonna use the same primers for the template whose Cs are changed to Ts in PCR?
Valeu!
@henrikslab
2 жыл бұрын
Not again... stop it, Mario! Thank you, man!
The video is very nice. However, I had not understood at first glance why U is converted into T in PCR. In another video, I saw that a complementary sequence is generated in a first-round, where U is paired with A. Then, in a second-round, the primary sequence is generated, but with T paired with A. It is equivalent to the conversion of U into T. I had confused because, in the cell, the U in DNA appears to be corrected into C. If the video showed the conversion of U into T in PCR it will be perfect!
@henrikslab
2 жыл бұрын
I agree! I decided to skip the step you mentioned ´cause I put the focus on the bisulfite conversion itself. But you described it correctly! I said "certain rounds of PCR" to simplify everything, but U is paired with A and this newly synthesized strand is paired with T then! True
love for that still
How do you know a given base was an un-methylated C and not a T? Do you to compare it the original sequence somehow?
@jinglin4358
9 ай бұрын
Yes. You compare post PCR sequence to pre. it’s possible to sequence whole genome with low concentrations of DNA ie extracted and not amplified DNA with next gen sequencing. So you can compare the sequence prior to bisulfite conversion and after.
I thought methylation mostly occurs at CpG islands alone?
@henrikslab
3 жыл бұрын
A CpG island is a region in the DNA with a high C G dinucleotide frequency and density. They are often located in promoter regions. Indeed, here we find an important part of methylation. You probably talk about CpG *sites*? Mainly methylation occurs at CpG sites, true. However, there is also methylation at CpA, CpT and CpG sites. See -> www.ncbi.nlm.nih.gov/pmc/articles/PMC5485512/
@alerookoh8748
3 жыл бұрын
Thank you for clarifying my question
My last like and last comment!
@henrikslab
4 жыл бұрын
Der Kritiker Ehre