I really like this Seminar and is there anybody who can give us these slides?
@HasnainBaqir-zq7xh17 күн бұрын
How we can get these slides?😊
@ahmedelawady75572 ай бұрын
Great talk ... Thank you
@alejandroyevenes69603 ай бұрын
The sound of the video is awful; I cannot understand what the speaker is saying.
@Risperi13 ай бұрын
3:51
@Risperi13 ай бұрын
19:23
@Risperi14 ай бұрын
10:00
@Risperi14 ай бұрын
15:40
@Risperi14 ай бұрын
28:08
@Risperi14 ай бұрын
34:00
@seanmcdonald32864 ай бұрын
Sorry this is unwatchable due to the sound
@pavithras94344 ай бұрын
Thankyou! I am a master thesis student in metabolomics and I was really confused between database vs libraries. Your video clarified a lot of doubts I was having, that I wasn´t able to get from reading even many research papers! Thanks again!
@albertofabbri15435 ай бұрын
Super interesting, thank you for the talk!
@jthoward936 ай бұрын
I could barely hear anything
@sendlazarus4307 ай бұрын
Do you test for MTFHR and COMT genetic morphisms?
@muhammadmusabsaood93077 ай бұрын
Much needed video. I am working on Qiacube HT in a Lab for first time and facing some issues related to vaccum pressure. Thanks for your video
@amasikorski7309 ай бұрын
Share slides next time, not speaker.
@iot31369 ай бұрын
Thank you 🙏 Excellent talk.
@saharosamamaray784610 ай бұрын
Great job! Dr Chen.
@JBanks33310 ай бұрын
📢 💨 👠💣💚
@raananikar Жыл бұрын
This was great.
@_mklein Жыл бұрын
Interesting presentation but the microphone sound is horrible! 😔
@user-bo1bb2cg5g Жыл бұрын
I have a question on the barcoding. When I take image of fluorescent particles with fluorescent microscope or confocal, we see a position shift between the 488 channel and all other channels. I don't know whether the imaging part of the nCounter system meets the same problem. If it does, the position of the blue dot from the image will misalign with all other channels. Then where should we place blue dot in the image? If we put it in the wrong place, we will get the wrong barcode.