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DIA-Umpire: comprehensive computational framework for data-independent acquisition proteomics.


ABSTRACT: 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.

SUBMITTER: Tsou CC 

PROVIDER: S-EPMC4399776 | biostudies-literature | 2015 Mar

REPOSITORIES: biostudies-literature

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DIA-Umpire: comprehensive computational framework for data-independent acquisition proteomics.

Tsou Chih-Chiang CC   Avtonomov Dmitry D   Larsen Brett B   Tucholska Monika M   Choi Hyungwon H   Gingras Anne-Claude AC   Nesvizhskii Alexey I AI  

Nature methods 20150119 3


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  ...[more]

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