1/6 TLDR thread for our "imaging-by-sequencing" work where we image at nanometer resolution without using cameras, lenses, fine scanning needles (like in scanning probe microscopes) or any light or electromagnetic radiation! How did we do this? More importantly, why?
Tapestry is a true example of inter-disciplinary, inter-institute collaboration enabled by enlightened leaders in positions of power @kvijayraghavan@jitumayor_lab. 🧵
This is the new world record for the largest 2D DNA origami lattice, ~18.75 cm²! It is assembled using ~one trillion individual DNA origami components.
https://t.co/fNN5hxLDd2 @ChemEurJ @AaltoResearch @HYBER_Aalto
"You truly get this holistic view of science that I’ve never seen in another lab. I feel incredibly lucky to be allowed to make these contributions here.” Become our next inventor. View current openings. #hiring#nowhiring#jobopenings
https://t.co/GvRCBWPi7E
https://t.co/u404kMFjoE TWO projects that I am a part of have made it to the XPRIZE finals! 1. Our single stranded RPA work (https://t.co/eaaITmcrhw) that is FAST (10 min) and SENSITIVE (4 cp!). 2. Tapestry pooling, collaboration led by my brother @manoj_333#XPRIZE#FINALS
Panel discussion at the Bangalore tech summit. My 12-minute presentation on Tapestry Pooling starts at 45 minutes. Would love to hear from experts and laypersons.
https://t.co/7AMwDbj59v
Do you have any questions about Tapestry pooling? Do you know someone who should know about it? Join us for this AMA by https://t.co/8prWzIoICP !
https://t.co/bgHwAkgM4j
So why are we so obsessed by centrosome asymmetry? It goes back to the work during my postdoc period (2007! ) that it is always the older, mother centrosome that stays in the stem cells, whereas the daughter centrosome goes to differentiating cell. 1/
https://t.co/6gUjOGliwP
This Week on Friday, October 9th, 2020 at 2 PM PST, We are hosting Dr. Nikhil Gopalkrishnan at Wyss Institute.
Talk Title "The Blind Cartographer: 'Imaging' with a DNA swarm".
Apply at https://t.co/ZoJ5Rhz9jo if you'd like to join and do not forget to share and retweet.
1/6 TLDR thread for our "imaging-by-sequencing" work where we image at nanometer resolution without using cameras, lenses, fine scanning needles (like in scanning probe microscopes) or any light or electromagnetic radiation! How did we do this? More importantly, why?