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024 7 _ |a 10.1021/acs.jproteome.3c00473
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024 7 _ |a 1535-3893
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037 _ _ |a DZNE-2024-00042
041 _ _ |a English
082 _ _ |a 540
100 1 _ |a Kardell, Oliver
|0 0000-0002-6703-7997
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245 _ _ |a Multicenter Collaborative Study to Optimize Mass Spectrometry Workflows of Clinical Specimens.
260 _ _ |a Washington, DC
|c 2024
|b ACS Publications
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520 _ _ |a The foundation for integrating mass spectrometry (MS)-based proteomics into systems medicine is the development of standardized start-to-finish and fit-for-purpose workflows for clinical specimens. An essential step in this pursuit is to highlight the common ground in a diverse landscape of different sample preparation techniques and liquid chromatography-mass spectrometry (LC-MS) setups. With the aim to benchmark and improve the current best practices among the proteomics MS laboratories of the CLINSPECT-M consortium, we performed two consecutive round-robin studies with full freedom to operate in terms of sample preparation and MS measurements. The six study partners were provided with two clinically relevant sample matrices: plasma and cerebrospinal fluid (CSF). In the first round, each laboratory applied their current best practice protocol for the respective matrix. Based on the achieved results and following a transparent exchange of all lab-specific protocols within the consortium, each laboratory could advance their methods before measuring the same samples in the second acquisition round. Both time points are compared with respect to identifications (IDs), data completeness, and precision, as well as reproducibility. As a result, the individual performances of participating study centers were improved in the second measurement, emphasizing the effect and importance of the expert-driven exchange of best practices for direct practical improvements.
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650 _ 2 |a Tandem Mass Spectrometry: methods
|2 MeSH
650 _ 2 |a Chromatography, Liquid: methods
|2 MeSH
650 _ 2 |a Workflow
|2 MeSH
650 _ 2 |a Reproducibility of Results
|2 MeSH
650 _ 2 |a Plasma: chemistry
|2 MeSH
650 _ 7 |a LC–MS
|2 Other
650 _ 7 |a LC–MS
|2 Other
650 _ 7 |a LC–MS
|2 Other
650 _ 7 |a CSF
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650 _ 7 |a LC–MS
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650 _ 7 |a R package mpwR
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650 _ 7 |a clinical specimen
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650 _ 7 |a data-dependent acquisition
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650 _ 7 |a data-independent acquisition
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650 _ 7 |a interlaboratory
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650 _ 7 |a intralaboratory
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650 _ 7 |a mass spectrometry
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650 _ 7 |a plasma
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650 _ 7 |a round-robin study
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700 1 _ |a von Toerne, Christine
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700 1 _ |a Merl-Pham, Juliane
|b 2
700 1 _ |a König, Ann-Christine
|b 3
700 1 _ |a Blindert, Marcel
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700 1 _ |a Barth, Teresa K
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700 1 _ |a Mergner, Julia
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700 1 _ |a Ludwig, Christina
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700 1 _ |a Tüshaus, Johanna
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700 1 _ |a Eckert, Stephan
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700 1 _ |a Müller, Stephan A
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700 1 _ |a Breimann, Stephan
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700 1 _ |a Giesbertz, Pieter
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700 1 _ |a Bernhardt, Alexander Maximilian
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700 1 _ |a Schweizer, Lisa
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700 1 _ |a Albrecht, Vincent
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700 1 _ |a Teupser, Daniel
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700 1 _ |a Imhof, Axel
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700 1 _ |a Kuster, Bernhard
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700 1 _ |a Lichtenthaler, Stefan F
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700 1 _ |a Mann, Matthias
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700 1 _ |a Cox, Jürgen
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700 1 _ |a Hauck, Stefanie M
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773 _ _ |a 10.1021/acs.jproteome.3c00473
|g Vol. 23, no. 1, p. 117 - 129
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