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
