多路复用
计算机科学
工作流程
串联质谱法
蛋白质组学
质谱法
计算生物学
数据采集
碎片(计算)
数据库搜索引擎
软件
数据挖掘
化学
色谱法
生物信息学
数据库
情报检索
生物
搜索引擎
程序设计语言
基因
生物化学
作者
Chih‐Chiang Tsou,Dmitry M. Avtonomov,Brett Larsen,Monika Tucholska,Hyungwon Choi,Anne‐Claude Gingras,Alexey I. Nesvizhskii
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2015-01-19
卷期号:12 (3): 258-264
被引量:639
摘要
The computational workflow of DIA-Umpire allows untargeted peptide identificationdirectly from DIA (data-independent acquisition) proteomics data without dependence on a spectral library for data extraction As a result of recent improvements in mass spectrometry (MS), there is increased interest in data-independent acquisition (DIA) strategies in which all peptides are systematically fragmented using wide mass-isolation windows ('multiplex fragmentation'). DIA-Umpire ( http://diaumpire.sourceforge.net/ ), a comprehensive computational workflow and open-source software for DIA data, detects precursor and fragment chromatographic features and assembles them into pseudo–tandem MS spectra. These spectra can be identified with conventional database-searching and protein-inference tools, allowing sensitive, untargeted analysis of DIA data without the need for a spectral library. Quantification is done with both precursor- and fragment-ion intensities. Furthermore, DIA-Umpire enables targeted extraction of quantitative information based on peptides initially identified in only a subset of the samples, resulting in more consistent quantification across multiple samples. We demonstrated the performance of the method with control samples of varying complexity and publicly available glycoproteomics and affinity purification–MS data.
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