Dear Chang,
One need to set resolution cut off, to have a meaningful data without
losing high resolution data and keeping data integrity. Some key quality
indicators like I/Sigma I,  CC 1/2 and Rpim etc., at outer most shell need
to be considered.  What was the CC 1/2 value in outer shell ?

Please refer to the below paper.
How good are my data and what is the resolution
Assessing and maximizing data quality in macromolecular crystallograph

On Sat, 11 Sep 2021, 9:52 pm Tao-Hsin Chang, <[email protected]>
wrote:

> Hi Farhan,
>
> It looks like that your diffraction data has an anisotropic issue and it
> leads to the issues of resolution limit, intensity, and completeness. Check
> The STARANISO Server (
> https://staraniso.globalphasing.org/cgi-bin/staraniso.cgi). It may be
> useful for your case.
>
> Best wishes,
> Tao-Hsin
>
> On Sep 11, 2021, at 11:55 AM, Syed Farhan Ali <[email protected]>
> wrote:
>
> Dear All,
>
> I have query regarding one of my dataset. I am running aimless by keeping
> highest resolution 1.62 A and getting  I/SigI = 2 but data completeness is
> around 22 in outermost shell. And if I am increasing the resolution cutoff
> up to 1.8 A then I/SigI is 6.2 and completeness is 82.4.
> I have attached the screenshot of the result.
> What should be the criteria to set the resolution limit?  Should I stick
> to  I/SigI  or I have to consider about the completeness of data.
> And if completeness is also a guiding factor than how much minimum
> completeness I can keep in the higher resolution shell.
>
>
>
>
>
> Regards,
> Farhan
>
>
>
>
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> <Screenshot 2021-09-11 at 8.43.25 PM.png><screenshot1.6.tiff>
>
>
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