Processing serial synchrotron crystallography diffraction data with DIALS.

4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology Methods in enzymology Pub Date : 2024-01-01 Epub Date: 2024-10-29 DOI:10.1016/bs.mie.2024.10.004
James Beilsten-Edmands, James M Parkhurst, Graeme Winter, Gwyndaf Evans
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Abstract

This chapter describes additions to the DIALS software package for processing serial still-shot crystallographic data, and the implementation of a pipeline, xia2.ssx, for processing and merging serial crystallography data using DIALS programs. To integrate partial still-shot diffraction data, a 3D gaussian profile model was developed that can describe anisotropic spot shapes. This model is optimised by maximum likelihood methods using the pixel-intensity distributions of strong diffraction spots, enabling simultaneous refinement of the profile model and Ewald-sphere offsets. We demonstrate the processing of an example SSX dataset where the improved partiality estimates lead to better model statistics compared with post-refined isotropic models. We also demonstrate some of the workflows available for merging SSX data, including processing time/dose resolved data series, where data can be separated at the point of merging after scaling and discuss the program outputs used to investigate the data throughout the pipeline.

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用DIALS处理串行同步加速器晶体衍射数据。
本章描述了对DIALS软件包的增加,用于处理串行静止镜头晶体学数据,并实现了一个管道,xia2。ssx,用于使用DIALS程序处理和合并串行晶体学数据。为了整合部分静止镜头衍射数据,建立了能够描述各向异性光斑形状的三维高斯剖面模型。该模型通过使用强衍射点的像素强度分布的最大似然方法进行优化,从而能够同时改进剖面模型和伊瓦尔德球偏移量。我们演示了对一个SSX数据集的处理,其中改进的偏性估计与改进后的各向同性模型相比可以获得更好的模型统计。我们还演示了一些用于合并SSX数据的工作流程,包括处理时间/剂量分辨数据系列,其中数据可以在缩放后合并时分离,并讨论了用于调查整个管道数据的程序输出。
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来源期刊
Methods in enzymology
Methods in enzymology 生物-生化研究方法
CiteScore
2.90
自引率
0.00%
发文量
308
审稿时长
3-6 weeks
期刊介绍: The critically acclaimed laboratory standard for almost 50 years, Methods in Enzymology is one of the most highly respected publications in the field of biochemistry. Each volume is eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. Now with over 500 volumes the series contains much material still relevant today and is truly an essential publication for researchers in all fields of life sciences, including microbiology, biochemistry, cancer research and genetics-just to name a few. Five of the 2013 Nobel Laureates have edited or contributed to volumes of MIE.
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