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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
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<div>[tanner@eris ~]> cat */XSCALE.INP<br>
OUTPUT_FILE=XDS_ASCII.HKL<br>
INPUT_FILE= ../XDS_ASCII.HKL<br>
INCLUDE_RESOLUTION_RANGE= 66.0 2.0 <br>
INPUT_FILE= ../../x-xx/XDS_ASCII.HKL<br>
INCLUDE_RESOLUTION_RANGE= 66 2.7<br>
[tanner@eris ~]> <br>
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<div>On May 4, 2016, at 6:00 AM, Sam Tang wrote:</div>
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<div dir="ltr">Dear colleagues<br clear="all">
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<div style="font-size:12.7273px">Hello again.</div>
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<div style="font-size:12.7273px">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</div>
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<div style="font-size:12.7273px">"Multiple intensity arrays - please specify one: data_labels=I,SIGI data_labels=IPR,SIGPR"</div>
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<div style="font-size:12.7273px">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?</div>
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<div style="font-size:12.7273px">Regards</div>
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<div style="font-size:12.7273px">Sam</div>
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<div style="font-size:12.7273px">Sam Tang</div>
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<div style="font-size:12.7273px"><font color="#000000">Biochemistry Programme, School of Life Sciences, CUHK</font></div>
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