If you used XDS to process the data, XSCALE is a good program for merging. It lets you specify the resolution ranges for merging. The output file goes directly into aimless for merging and conversion to F. The script is simple, such as [tanner@eris ~]> cat */XSCALE.INP OUTPUT_FILE=XDS_ASCII.HKL INPUT_FILE= ../XDS_ASCII.HKL INCLUDE_RESOLUTION_RANGE= 66.0 2.0 INPUT_FILE= ../../x-xx/XDS_ASCII.HKL INCLUDE_RESOLUTION_RANGE= 66 2.7 [tanner@eris ~]> On May 4, 2016, at 6:00 AM, Sam Tang wrote: Dear colleagues Hello again. I would like to scale and merge two different native datasets for a same protein complex (which semed to die off gradually in the beam) using the scale_and_merge tool. The error message was received "Multiple intensity arrays - please specify one: data_labels=I,SIGI data_labels=IPR,SIGPR" However I looked into the log file and I have actually included "data_labels = "IPR,SIGIPR,merged" . Perhaps I have missed something else in the setting? Regards Sam Sam Tang Biochemistry Programme, School of Life Sciences, CUHK _______________________________________________ phenixbb mailing list [email protected]mailto:[email protected] http://phenix-online.org/mailman/listinfo/phenixbb Unsubscribe: [email protected]