This chapter focuses on the mass spectrometry data processing workflow. The first step consists of processing the raw MS data, leading to a feature matrix amenable for statistical analysis. The raw MS files contain the list of spectra acquired during the run, and each spectrum contains many pairs. In the field of metabolite fingerprinting, Direct Infusion Mass Spectrometry and Flow Injection Mass Spectrometry can be used to complement chromatography-based MS techniques. To reduce this complexity, several feature detection algorithms have been developed. A feature is characterized by a retention time, an m/z value and an intensity. In microarray data analysis it is relatively straightforward to compare the expression of some genes in one sample against the expression in a second one, because the RNA is hybridized to a particular “known” probe sequence. In case an accurate-mass spectrometer has been used, it is also important to determine the mass accuracy in the measurements
Neumann, S.; Yanes, O.; Mumm, R.; Franceschi, P. (2019). Mass Spectrometry Data Processing. In: Metabolomics: practical guide to design and analysis (editor(s) Wehrens, R.; Salek, R.): Taylor & Francis: 73-99. handle: https://hdl.handle.net/10449/95995
Mass Spectrometry Data Processing
Franceschi, P.Ultimo
2019-01-01
Abstract
This chapter focuses on the mass spectrometry data processing workflow. The first step consists of processing the raw MS data, leading to a feature matrix amenable for statistical analysis. The raw MS files contain the list of spectra acquired during the run, and each spectrum contains many pairs. In the field of metabolite fingerprinting, Direct Infusion Mass Spectrometry and Flow Injection Mass Spectrometry can be used to complement chromatography-based MS techniques. To reduce this complexity, several feature detection algorithms have been developed. A feature is characterized by a retention time, an m/z value and an intensity. In microarray data analysis it is relatively straightforward to compare the expression of some genes in one sample against the expression in a second one, because the RNA is hybridized to a particular “known” probe sequence. In case an accurate-mass spectrometer has been used, it is also important to determine the mass accuracy in the measurements| File | Dimensione | Formato | |
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Ch. 4: Mass Spectrometry Data Processing.pdf
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