Dear Gottfried, I think you should take this up with Rigaku. They might have a re-formatting program for .ref files, and/or they may be able to tell you how to process the Saturn92 data with XDS (I can hardly imagine that they changed the format in a XDS-incompatible way).
But you paid for the machine, and that should entitle you to their service. good luck, Kay On Sun, 15 Oct 2017 13:35:34 +0200, Gottfried Palm <p...@uni-greifswald.de> wrote: >Dear all, > > this is a question about scaling data integrated in CrystalClear >(Rigaku data processing gui based on d*trek) in ccp4. >Since scaling dtprofit.ref files from different scans is sometimes poor >or even failing within CrystalClear (i.e. with dtscaleaverage after >merging them), I used to try scaling them with scala. I am facing this >problem mainly with high resolution / small molecule data collection, >where I need up to 20 scans, each 90-180 degrees, for complete low and >high resolution. > >The procedure, that worked, was using > >dtrek2scala for each scan (with scan1.ref and output_scan1.head, then a >second run of dtrek2scala for scan2.ref and output_scan2.head, etc.) to >create scan1.mtz, scan2.mtz, etc. >sortmtz with scan1.mtz, scan2.mtz, ... to create a multibatch mtz file >scala with the multibatch.mtz file to create the final scaled mtz file > >Some time ago Rigaku changed the format of the .ref files, so >dtrek2scala is not working any more. >Is there a possibility to change the new .ref format to the old one? Or >can I read the new .ref files in scala or better aimless directly? > >The alternative to process the images in xds hits a similar problem: The >format of the images has also changed and the new .img files (from the >Saturn92 detector) are not read anymore (whereas they used to be >processable in xds before). > >Greetings > Gottfried > > >Dr. Gottfried Palm >Ernst-Moritz-Arndt-Universität >Inst. für Biochemie (MNF) >Abt. Biochemie I >Felix-Hausdorff-Straße 4 >17489 Greifswald
