NGS Sequencing: Understanding Gene Coverage and Read Depth

[@MallikaVenkatramani]

As a genetic counselor in-training - I really appreciate this! Thank you!

[@abumohammed9659]

Thank you so much I was not sure about genome coverage before I see this amazing video !!!!!!

[@ZiggyMercury]

Great video, thanks!
One small correction: at 3:12 you say: "when I sequence a sample at 100X depth, and if the tumor [mutation] content is around 20%, at least 200 fragments will show up a mutation". I think it should be "20 fragments" and not "200 fragments", no?

[@Kabirr]

yeah you make sense

[@noureddineIDALI]

yeah thats true

[@sabaiqbal8873]

Excellent Sir. keep posting such a shot videos for easy understanding plz

[@shreyaverma1699]

Thank you

[@aartihansda8352]

Thank you for the video.

[@AnkushSharma-zv5hv]

thanks for easy explanation

[@N5033]

Best ever

[@MrRamaeri]

Thank you so much, 🥇🥇🥇🥇🥇🥇🥇🥇🥇🥇🥇🥇🥇🥇🥇

[@aang7505]

thank you very much!