Hi all,
I have a question on how to combine two dataset from different crystal
of the same protein.
The first way I could think of is that,
1) Merge two dataset seperately;
2) Scale them to see whether they are consistent with each other
enough as indicated by the R-factor;
3) If the R is low enough, say below 10 or 15%, then take the average
for both the F and SIGF.
The other way is that,
1) Take the unmerged file from MOSFLM, and reset their batch number;
2) Run SCALA to scale these two unmerged dataset at the same time.
Could anyone tell which way is the better or the correct way?
Thank you in advance!
Alphar
