Hi Liliana,

a few things to consider:

0) There is a Phenix mailing list for Phenix specific questions (phenixbb);

1) Bin completeness depends on (obviously) how binning is done (number of
reflections per bin or number of bins or binning in d^2 or d^3 spacing or
log-binning etc etc etc) -- all of this will affect the number of
reflections in the "highest resolution bin" and corresponding statistics.
And..."how binning is done" wildly differs by the program used or even
within the same program!

2) Refinement (in Phenix) as well as many other Phenix tools apply
temporary reflection omission according to the Read (1999) paper (Acta
Cryst. (1999). D55, 1759-1764). This means while you have so many
reflections in your input reflection file, the actual reflections used in
calculations and reported statistics may be different. Most logs files keep
a good record of this, meaning you can track this down by inspecting logs
files carefully.

Let me know if you need more assistance with this issue.

Cheers,
Pavel

On Wed, Jan 17, 2024 at 1:43 PM David Briggs <david.bri...@crick.ac.uk>
wrote:

> Hi Liliana,
>
> Two things leap out at me when I look at your data summary.
>
> (1) Your data probably do not go to 1.77Å. The CC1/2 in your outer shell
> is below any of the usual thresholds. There are discussions to be had about
> what the threshold is, but normally CC1/2 values of 0.5 or sometimes 0.3
> are used. You should also consider I/sigI.
>
> (2) I believe that by default Phenix.refine excludes weaker reflections
> from refinement, which leads to the discrepancy in completeness statistics.
> As your data do not extend as far as what is contained in your mtz file,
> Phenix excludes those essentially "empty" reflections. Judging by the
> Phenix refine output, I would estimate your data goes to somewhere around
> 1.9Å
>
> The program Pairef can help inform your choice of high-resolution cutoff.
>
> This can be run from CCP4cloud, but is also available for Phenix, I
> believe.
>
> See https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248825/
>
> Hope this helps,
>
> Dave
>
>
> *Dr David C. Briggs CSci MRSB*
>
> Principal Laboratory Research Scientist
>
> Signalling and Structural Biology Lab
>
> The Francis Crick Institute
>
> London, UK
>
> ==
>
> about.me/david_briggs
> ------------------------------
> *From:* CCP4 bulletin board <CCP4BB@JISCMAIL.AC.UK> on behalf of Liliana
> Margent <lmarg...@gradcenter.cuny.edu>
> *Sent:* Wednesday, January 17, 2024 9:19:36 PM
> *To:* CCP4BB@JISCMAIL.AC.UK <CCP4BB@JISCMAIL.AC.UK>
> *Subject:* [ccp4bb] Resolution Discrepancy in Data Set
>
>
> External Sender: Use caution.
>
>
> Hello all,
>
> I hope this message finds you well.
>
> In my current data set, I’ve encountered a discrepancy between the
> completeness in the high-resolution shells in merged statistics vs the
> refinement statistics. For example, when I look at my merged statistics
> file, output by Xia2 dials, the completeness in the high-resolution shells
> are 97.6%. When I take this data and subsequently refine it in PHENIX I get
> extremely different completeness ranges in the high-resolution shells, but
> I cannot figure out why this large difference is occurring. I’m reaching
> out to you, our esteemed community, for any insights or advice you might
> have. Has anyone else faced a similar challenge? If so, how did you
> navigate through it?  Your experiences and suggestions could be invaluable
> in helping me understand and resolve this issue.
>
> Thank you in advance for your time and expertise.
>
> Best regards,
> Liliana
>
> see a side-by-side image of the files I mention in the message in
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