Hi all, I am wondering what the best practice is to compare datasets that are of the same protein but different quality, for instance 2 vs. 3 A.
I know that truncating the structures to the same resolution bin is alright, but the data quality in the lower resolution bins are also not the same. Is there a way to "inject" noise into the data such that the bins are more similar? These datasets cannot be recollected at higher resolution since they are collected at increasingly high pressure, and the resolution change is anticorrelated with the pressure; no way to get around crystal stability. Any suggestions are appreciated, Matt ######################################################################## To unsubscribe from the CCP4BB list, click the following link: https://www.jiscmail.ac.uk/cgi-bin/WA-JISC.exe?SUBED1=CCP4BB&A=1 This message was issued to members of www.jiscmail.ac.uk/CCP4BB, a mailing list hosted by www.jiscmail.ac.uk, terms & conditions are available at https://www.jiscmail.ac.uk/policyandsecurity/
