Cool, typed a long reply but only about 1/3 of it is still relevant and is 
given below.

The crystal would have to be capillary mounted for these data collections or 
the humidity controlled somehow. Only 253 K would be a good one to use. 
Pre-cryo, this used to give good data at SRS! Interested in the oil method you 
mentioned. Anyway, for capillary work:

253 K = -20 C = good temp to use
273 K = 0 C = maybe OK
293 K = 20 C = OK
313 K = 30 C = maybe OK

> Re: In addition, I computed the wilson B.s
253 - 41
273 - 35.4
293 - 36.5
313 - 0.19

Assuming the last one is a typo, unless it's a neutron dataset - no B-factor ;-)

Cheers, Jon.C.

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-------- Original Message --------
On 8 Sep 2022, 14:39, Matt McLeod wrote:

> Hi all, This is my first JISC post so I am still working on how to navigate 
> this. I have to say I feel like there is a much better way to have a forum on 
> structural biology... I could imagine a discord server where we can post 
> individual questions, have live chats, etc. I'd be happy to set this up if 
> people are interested. The data collection was done on a single crystal, 
> using vector scanning to minimize radiation damage, and using oil to prevent 
> dehydration. I have since gone back and re-processed the 313K dataset with an 
> updated DIALS and the problem seems to have gone away (and gave me better 
> scaling statistics)...my guess is that the scaling program is just improving 
> some of these "bugs". This high temp dataset now has the highest average 
> B-factor. Regardless, there does seem to be not much variation with the 
> temperature at the modest temperatures which may be in line with the 
> biological story but these values make much more sense now. Thanks everyone 
> for all the suggestions with regards to scaling the data together, SCALEIT, 
> etc. I have a few different options to interpret the data now. Matt 
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