I’d be with you, Graeme, as a good compromise between merged data and raw 
diffraction images.  Though it does seem to be getting more practical to make 
image data available…

Randy

-----
Randy J. Read
Department of Haematology, University of Cambridge
Cambridge Institute for Medical Research    Tel: +44 1223 336500
Wellcome Trust/MRC Building                         Fax: +44 1223 336827
Hills Road                                                            E-mail: 
[email protected]
Cambridge CB2 0XY, U.K.                               
www-structmed.cimr.cam.ac.uk

> On 20 Mar 2019, at 12:31, [email protected] 
> <[email protected]> wrote:
> 
> Hi Eleanor
> 
> I’d raise you scaled but unmerged intensities :-)
> 
> Best wishes Graeme
> 
> 
> On 20 Mar 2019, at 12:21, Eleanor Dodson 
> <[email protected]<mailto:[email protected]>>
>  wrote:
> 
> 
> Wouldn't it be a good idea if the pdb required that data deposition provide h 
> k l I+ SIGI+  I- SIGI-  ??
> 
> Even if the depositor has not exploited the anomalous signal, it may well be 
> there sufficiently strongly to validate CYS or phosphates.
> 
> I believe aata processing programs provide this information ?
> 
> Eleanor Dodson
> 
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