Dear all,
I'm dealing with anisotropic diffraction of a membrane protein.
I've read from previous threads that it is better to not cut off any
data, and that aimless doesn't anisotropically scale the data any way.
So my question is: given my anisotropic diffraction, what resolution
cutoff do i
Hi Vincent,
my advice is: if in doubt, scale at the highest of those resolution choices.
This way you don't have to go back to scaling later. There is no harm in using
the highest resolution. Don't let yourself be fooled by Rmerge.
best,
Kay
On Thu, 19 Jul 2012 17:52:14 +0200, vincent Chaptal