[phenixbb] (no subject)
pafonine at lbl.gov
Thu Jul 29 12:02:31 PDT 2021
Also, see some discussion around Table 1 here:
Different methods exist to split reciprocal space in resolutions shells:
by volume, by shell width, by number of reflections and so on. Their
utility depends on specific context. I'm not aware of specific guidances
nor rules for defining the highest resolution bin.
On 7/29/21 08:05, Johannes Cramer wrote:
> I think most programs just divide the number of reflections by 10 (or
> however many shells you want there to be) and make it so that all
> shells contain the same number of reflections.
> Am Mi., 28. Juli 2021 um 21:10 Uhr schrieb Pavel Afonine
> <pafonine at lbl.gov <mailto:pafonine at lbl.gov>>:
> Hi Smita,
> > Can someone suggest to me, how we can decide the
> > resolution range in the outer shell during the protein crystal data
> > set.
> the choice is pretty arbitrary. Typically the software chooses it for
> you and it is fine most of the time.
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