Dear All,
I tried symmetry expansion on my dataset followed by refinement in C1. The resulting map FSC looked too good to be true (I got ~3 Angs according to FSC cut-off of 0.143), and upon closer inspection of the map I could see that the resolution was much worse than the non symmetry expanded particles refined in the symmetry of the protein (~3.9Angs).
Any ideas why this is happening? Am I doing something wrong?
When I repeated the run without a mask from a previous refinement that seemed fine, the expanded particles refinement hits nyquist! but again looks terrible.
Best,
Omid