Genetic Markers | RAPD, RFLP, AFLP

This lecture on genetic markers explains about RAPD, RFLP, AFLP markers and the use of these markers in genetic fingerprinting, SNP detection and plant breeding.
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can you do a video about Sequence Tagged Sites (STS) and type of STS in detail!
SSR, SCARs, CAPs and ISSR and their differences!
thank you.

[@장혜원-f1m]

Sir thank you so much I finally got the concept of AFLP!

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Thnku soo much sir for your great explanation💐

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[@anuragmishra3654]

Hey! Small thing I would like to point out. The rflp fragments you show on the sketch are all equal in length where you mark the RE sites. Wont separate on gel. :) Also the smaller three fragments would migrate much faster than the two large ones.
Thanks for the very well illustrated explanation.

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Vry effective way of teaching... Hat's of to u..

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From Bangladesh 🇧🇩

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Very good for senior students and faculty who came from different specialization. Keep it up.

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Very helpful...and also I have perceive some concep from your video thank you sir..

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sir thanks for helping us in zoology as optional in UPSC

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tomorrow is my PBG exam.....thnq so much for making this video 😍........you are really a good teacher....whatever you taught us it seems like very easy and simple......bt in college I don't understand anything.....our college teachers even make a simple thing very complex

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That was a great explanation...
very helpful!
thank you...

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Your explanation is superb and understood it clearly ........super bro👌

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Thank you so much sir very easy explanation by u .

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thanks a lot sir, now I know the difference...

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Tq sir for
watching ur Pdf lesson that provide me to understand easily... and give to multiple video lessons from different characters abt on biotechnology genetics relateds.

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I miss your Frontech headphones

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good at all

[@PuspaAlmas]

i skipped my genetic class 2 times and this video is very helpful, thank you sir!

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Thank u . i just watch it and got much more idea about these stuffs .

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Thanku so much sir

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thnk u soo much sir...it is vry helpful...nd it has cleared my all confusions....

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Thank u so much sir this video is very helpful .

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Thank you so much

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Thank you very much. It is very usefull for me

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[@mrinusand]

thankyou so much Bhaiya, helping me for tomorrow's genetic engg exam!

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Thank you sir

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Learning more than in school!

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Please also upload video on Use of ITS, MatK and rbcL in Angiosperm Taxonomy

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Thank You sir!!💯

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[@pamarthijayakrishna2737]

It Was so easy to understand. Thanq sir

[@abswiter1]

The number of DYS what it does indicate ??
For exemple DYS394
Is it the molecular weight?

[@arpitagill5718]

In the RAPD technique only the primer that is complementary will bind to the sequence ?

[@nadaamr5719]

thank you very much this video has helped me a lot god bless you

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[@alisaha8518]

You are great!!!!!
😀

[@nimnankit]

Wow amazing sir u r so brilliant....

[@zoyeb100]

Sir for RFLP do we extract whole DNA of a cell (6+ billion bp) and restrict it with a restriction enzyme? Or do we extract only a part of the entire DNA and then restrict it? If so how do we do it

[@Rainaraina1234]

Sir RAPD ka kuch clear nai kiya kaisay kaisay marking main help karta hau

[@AbdulAziz-bg2jy]

U r an excellent teacher👌

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[@keshavjha4477]

thanx for such nice videos... can us explain about how can we locate a mutation without doing an expensive genome sequencing

[@nikhilkeshri3759]

Hey.. The random primee tht we r destined to add in rapd fr pcr thereafter..is it necessary to do so.. I mn that the primer cn b run in pcr evn to gt aplified no directly..?????

[@prashantadhau903]

Please sir make a video on "Maxam and Gilbert technique of DNA sequencing"

[@shomusbiologyofficial]

It's already made

[@prashantadhau903]

@@shomusbiologyofficial thanks sir.. I'll search it

[@aimenmehmood8288]

which type of nuclease enzyme is best to use for degrading all DNA in a sample??
plz explain
and one more
you want to degrade all DNA in a sample to avoid contamination..will you use exonuclease or endonuclease and what will be the reason for selection??
plz explain my questions

[@vaishalithukral9129]

I have a doubt. In AFLP, if we already know about the restriction enzyme sequence flaking the sequence of interst, why do we need adaptors. We can simply use primers against those restriction sequences. Please do reply

[@dr.md.ismailhossain2681]

Very good lecture but we have to should short discuss.

[@rajeshthavi8827]

Explained in very simple language. Easy to understand.
But You've used only half of the screen. So board was not clearly visible...

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thank you for amazing explanation

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It's like Raj Koothrappali got jealous on Fun with Flags.

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LMAO this comment is gold xD

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HAHAHA

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Lol

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😆

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Brooo !!!!!! 🤣😂😅🤣😅😅

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excellent explanation!

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Thank you

[@bhu2011]

I have a querry,...is it not that we don't require sequence information in AFLP too..just the adapter sequence is sufficient

[@prashpp]

May be, it should be known to select the particular Restriction Enzyme , which do not cleave our Target DNA. I don't know,it's just a guess.

[@yogeshanjansinger2872]

Sir, please can you explain in Hindi video, please sir. 🙏🙏

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I wanted this comparison... thank u....

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Glad it helped

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Thank you sir. It is helpful

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Thanks

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thank u sir....
happy new year sir

[@spiritualseeker999]

Amazing explaination sir.. thankyou

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You're welcome

[@tanvisharma812]

Thank u for the lectures.... But pls can u emphasize more on RAPD with more examples

[@ravikumarspatil5080]

after isolation of DNA from both control and stress plants. If we go for RAPD analysis of such DNA is any difference in the polymorsphism..?

[@d.j..2149]

Firstly thank you sir..how can be Target sequence identify

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Thank you

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Koothrappali kills it again!!

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Excellent Sir.

[@mahlettadesse230]

wow unique explanation....

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Thank you for teaching 😃 .

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[@AshhadMunir20]

Well described.. but please improve your sound quality

[@rehababdelaziz4296]

trrwrrtowbcv b

[@rameshkandasamy6716]

thank u sir for simple explanation.. one doubt ..which genetic marker is called PCR based?

[@rabinapraj1821]

If multiple times target DNA present, since it has same length, rather than getting multiple bands, we will be getting dense bands ryt?! Pls clear that area sir 🙏

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Thkuuu 👨 sir

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U r the best 😎

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Sir vntrs pay koe complete video nae hay apki? Sir must reply plz

[@lakshmigayathrir4135]

Am unable to understand how random amplification of dna helps in preselection of breeds.Can u explain that concept further?

[@suresheedunuri2917]

Hi sir you have tell about distinguish between these three techniques but this is not enough it requires more emphasis on how three techniques are different, this explanation seems like these three techniques are useful for same purpose, you should have explain actually what is the main purpose of these 3 techniques and how they exactly distinguish this is important thing because
In molecular biology techniques some times seems all techniques are useful for same purpose that's why I am emphasizing on purpose & distinguish

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Thank you sooooo much stay blessed and keep making such videos... :)

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+senorzorro12 thank you. Glad you liked my lectures