Best Practices for Evaluating Similar Protein Maps

Dear Colleagues,

I have obtained quite similar results for one protein, with a slight difference in resolution. At first glance, the observed differences are primarily related to:
a) A resolution difference of 0.10 Å
b) B-factor small variations

The results were derived using non-uniform refinement and local refinement methods.

Given this, is there a clear method or criterion to better discriminate between such similar results? Additionally, which map should ultimately be considered the most reliable or “best” one? (By best, I mean resolution, integrity, etc.)

Thank you for your insights.

Kind regards,
Dmitry