Gratz on the first paper!

Thanks! Yeah, my old method of adding an overhang on cadnano to find it on oxDNA was painful xD It's remains a little hard for us to iterate between the (s)cadnano strand-routing map design to the 3D oxDNA with our off-lattice ATHENA wireframes. But, you've already makes my life waaaay easier

oh that scadnano integration is great, thanks, I'd hadn't noticed it before

Awesome! Do you guys have any tips on how you orientate yourselves when editing between cadnano and visualizing/relaxing in oxDNA? I often find it really hard to locate what I've changed in our highly symmetric structures on cadnano (might be more of a problem with our symmetric wireframes)

Actually come to think of it, its gotta be the protein. That dye on it's own would be soooooo absorbing

I think it's the protein. There's a big farm complex in Germnay that makes them at scale. Gonna doubt dye survives for that long on it's own.

I think back in the UK we've substitution that blue dye for it bio-derived bilins in lots of sweets. But, its transition dipole's just not as fun :(