Genomics In India

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@SalmanMansour-w6g 6 күн бұрын

I stoped listening to you and start dancing, I can’t hear u bro

@medicalmarvels976 15 күн бұрын

great

@GGokul-j6h 2 ай бұрын

Radha mam very talent doctor in neurologist

@sojulalsasidharan4800 3 ай бұрын

Thank for your finding.. am one of the affected person of the same disease....

@ashalatharadhakrishnan5024 7 ай бұрын

Great dear Radha, proud of you always

@sandeepb9397 8 ай бұрын

building own careers and glorifying own resume with tax payers money ! Keep it up

@sandeepb9397 8 ай бұрын

building their own resumes and careers with taxpayer money. rest all is hogwash

@seemabiswas6919 9 ай бұрын

Hi Dear Dr. Shrey Gandhi. Myself Dr. Seema Biswas ( MD Pathology , Presently Fellow in Molecular Hemato oncopathology) . How I can apply for workshop if in any recently in future

@samathamathew8153 9 ай бұрын

Is it Communicable by any chance...?

@sheraziz147 10 ай бұрын

Excellent video

@CHILDBRAINHOSPITAL 10 ай бұрын

Thank you Professor Helen. Always inspiring

@divyaganesh1729 11 ай бұрын

my baby died due to this syndrome

@djmohmand 11 ай бұрын

Dear Indians, Nice work. Keep it up.

@pushpalathamanjunatha7810 Жыл бұрын

Excellent presentation, I was looking for something like this for almost a year. Thanks

@gilsonborrgess6262 Жыл бұрын

Very good🎉 You explained very well, thanks

@kakhangchungpanmei8205 Жыл бұрын

Thank you. That was a fine and interesting presentation.

@tamrinimelda Жыл бұрын

Permohonan kepada sudin LH atau sudin kesehatan >>> lakukanlah penutupan bagian atas saluran got yang ada di depan pesantren ekonomi darul uchwah, kedoya selatan, jakarta barat #salamTAMRINgantenk

@rajanduda9532 Жыл бұрын

Brilliant.

@Intradimtraveller Жыл бұрын

awesome class mercy..

@Intradimtraveller Жыл бұрын

great lecture mercy

@mirzamudassir3937 Жыл бұрын

Very informative

@Sajee32 Жыл бұрын

Thanks for the lectures. I am a PhD scholar with a background in Physics and currently working on protein sequencing. This lectures are really helpful. Keep going.

@Sajee32 Жыл бұрын

Amazing lectures. Thank you.

@Dolapo_Olugbile Жыл бұрын

very informative!

@sanathprasad9154 Жыл бұрын

it was a really good presentation and more information coud be provided on indian variants present

@DivyaDivya-mr8se Жыл бұрын

Mam Application of genetics counselling in animal cell culture topic pr lecture upload kr do

@drpallavijain5057 Жыл бұрын

Nice video Sir. GVACI has indeed made NGS very interesting

@ravanthreddyful Жыл бұрын

Ma'am my father is suffering from mitochondrial disease,he is going to critical stage,plz help and give contact of Vishu Gupta ji

@sathyamevajayathe1544 Жыл бұрын

Very good, 😊

@angalenar8018 Жыл бұрын

Very clear explanation...thankyou

@karuppusamyk6197 Жыл бұрын

very informative ,keep your good work

@AyeshaKhan-ip1kh Жыл бұрын

Because in routine diagnostics set up for solid tumors...it's not feasible to look at all these points for each CNV

@AyeshaKhan-ip1kh Жыл бұрын

Is there any CNV calculation software available online other than CINGEN?

@AyeshaKhan-ip1kh Жыл бұрын

Hi mam ..is this 5 tier classification applicable for malignant neoplasms??? Is there any database for CNVs?

@GenomicsInIndia Жыл бұрын

Questions can be asked in this chat box.

@ASR890 Жыл бұрын

Very nice 👍

@himanshuranjan9276 Жыл бұрын

Hello everyone ☺️☺️

@BeUbuntu 2 жыл бұрын

Nice presentation 🙌

@anjaligupta6180 2 жыл бұрын

Brilliant session👏

@poornimasivamani1778 2 жыл бұрын

Will you perform the genetics test seperately for nuclear gene and mitochondrial gene ?

@VinodScariaLab 2 жыл бұрын

Yes.

@ravanthreddyful Жыл бұрын

@@VinodScariaLab Plz give your contact sir,my father has suffering from mitochondrial disease

@vishugupta7426 2 жыл бұрын

Questions can be posted here in live chat, we will answer them here

@shivampandey5658 2 жыл бұрын

Can we ask questions in the webinar?

@ashavinay7707 2 жыл бұрын

THANK YOU FOR THE LECTURE,HOW DO WE OBTAIN RSID FROM NMID/NPID

@asishswain1259 2 жыл бұрын

lower the background music

@ektajajodia1241 2 жыл бұрын

Thank you Anjali. You have explained everything very beautifully. I have a question though: how do we know whether the two mutations identified in a gene is in cis or trans.

@anjalibajaj4947 2 жыл бұрын

Thankyou for the encouraging feedback. Simplest way to know the status of two variations is by testing parents. If both the variations are coming from the same parent, then it will be cis condition. On the other hand, if both the parents are contributing one variation each, then they will be on different chromosomes in child, hence, trans condition.

@ektajajodia1241 2 жыл бұрын

@@anjalibajaj4947 thanks. But i wanted to know whether its possible to identify cis and trans in the NGS bioinformatics?

@anjalibajaj4947 2 жыл бұрын

@@ektajajodia1241 Yes it is possible to know the cis/trans status using NGS data. You can visualise the reads spanning the variants using Integrative Genomics Viewer (IGV). If both the variants are captured in the same read then they are in cis position (same copy of the chromosome). If they are lying in separate reads then they may be in trans. For using this approach, the variants should lie close to each other to be able to get captured in same read. Please check Figure 4 in this article for your reference pubmed.ncbi.nlm.nih.gov/26295337/

@vishugupta7426 2 жыл бұрын

Correction at 17:09 : The ratio 1.5 depicts heterozygous duplication and ratio 2 depicts the homozygous duplication.

@mohamedrafi8572 2 жыл бұрын

My both children have hyper igd syndrom

@GenomicsInIndia Жыл бұрын

If you are in Kerala, the Department of Pediatrics at Govt Medical College , Kozhikode has specialised care and genetic testing for.Hyper IgD

@cjolly4620 2 жыл бұрын

👍💐💐💐

@mellisachan2653 2 жыл бұрын

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