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Colocalization Features for Classification of Tumors Using Desorption Electrospray Ionization Mass Spectrometry Imaging
Author(s) -
Paolo Inglese,
Gonçalo dos Santos Correia,
Pamela Pruski,
Robert C. Glen,
Zoltán Takáts
Publication year - 2019
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/acs.analchem.8b05598
Subject(s) - colocalization , mass spectrometry imaging , chemistry , pattern recognition (psychology) , mass spectrometry , artificial intelligence , sample (material) , segmentation , maldi imaging , biological system , mass spectrum , computer science , chromatography , matrix assisted laser desorption/ionization , desorption , organic chemistry , adsorption , biology , microbiology and biotechnology
Supervised modeling of mass spectrometry imaging (MSI) data is a crucial component for the detection of the distinct molecular characteristics of cancerous tissues. Currently, two types of supervised analyses are mainly used on MSI data: pixel-wise segmentation of sample images and whole-sample-based classification. A large number of mass spectra associated with each MSI sample can represent a challenge for designing models that simultaneously preserve the overall molecular content while capturing valuable information contained in the MSI data. Furthermore, intensity-related batch effects can introduce biases in the statistical models. Here we introduce a method based on ion colocalization features that allows the classification of whole tissue specimens using MSI data, which naturally preserves the spatial information associated the with the mass spectra and is less sensitive to possible batch effects. Finally, we propose data visualization strategies for the inspection of the derived networks, which can be used to assess whether the correlation differences are related to coexpression/suppression or disjoint spatial localization patterns and can suggest hypotheses based on the underlying mechanisms associated with the different classes of analyzed samples.

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