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<p>Also, see some discussion around Table 1 here:</p>
<p><a class="moz-txt-link-freetext" href="https://journals.iucr.org/d/issues/2013/04/00/dz5273/dz5273.pdf">https://journals.iucr.org/d/issues/2013/04/00/dz5273/dz5273.pdf</a></p>
<p>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.</p>
<p>Pavel<br>
</p>
<div class="moz-cite-prefix">On 7/29/21 08:05, Johannes Cramer
wrote:<br>
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cite="mid:CAHDfKqbR_Y_6XorSEgkftP1EtfU6K3Uw6kgM91wYbbmica+p0A@mail.gmail.com">
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<div dir="ltr">Hi,
<div><br>
</div>
<div>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. </div>
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<div>Cheers, </div>
<div>Johannes</div>
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<br>
<div class="gmail_quote">
<div dir="ltr" class="gmail_attr">Am Mi., 28. Juli 2021 um
21:10 Uhr schrieb Pavel Afonine <<a
href="mailto:pafonine@lbl.gov" moz-do-not-send="true">pafonine@lbl.gov</a>>:<br>
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<blockquote class="gmail_quote" style="margin:0px 0px 0px
0.8ex;border-left:1px solid rgb(204,204,204);padding-left:1ex">Hi
Smita,<br>
<br>
> Can someone suggest to me, how we can
decide the<br>
> resolution range in the outer shell during the protein
crystal data<br>
> set.<br>
<br>
the choice is pretty arbitrary. Typically the software chooses
it for <br>
you and it is fine most of the time.<br>
<br>
Pavel<br>
<br>
<br>
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