Scaling and assessment of data quality

被引:4040
作者
Evans, P [1 ]
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
来源
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 2006年 / 62卷
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
D O I
10.1107/S0907444905036693
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The various physical factors affecting measured diffraction intensities are discussed, as are the scaling models which may be used to put the data on a consistent scale. After scaling, the intensities can be analysed to set the real resolution of the data set, to detect bad regions ( e. g. bad images), to analyse radiation damage and to assess the overall quality of the data set. The significance of any anomalous signal may be assessed by probability and correlation analysis. The algorithms used by the CCP4 scaling program SCALA are described. A requirement for the scaling and merging of intensities is knowledge of the Laue group and point-group symmetries: the possible symmetry of the diffraction pattern may be determined from scores such as correlation coefficients between observations which might be symmetry-related. These scoring functions are implemented in a new program POINTLESS.
引用
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页码:72 / 82
页数:11
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