Literature DB >> 19228047

Discriminating variable test and selectivity ratio plot: quantitative tools for interpretation and variable (biomarker) selection in complex spectral or chromatographic profiles.

Tarja Rajalahti1, Reidar Arneberg, Ann C Kroksveen, Magnus Berle, Kjell-Morten Myhr, Olav M Kvalheim.   

Abstract

The discriminating variable (DIVA) test and the selectivity ratio (SR) plot are developed as quantitative tools for revealing the variables in spectral or chromatographic profiles discriminating best between two groups of samples. The SR plot is visually similar to a spectrum or a chromatogram, but with the most intense regions corresponding to the most discriminating variables. Thus, the variables with highest SR represent the variables most important for interpretation of differences between groups. Regions with variables that are positively or negatively correlated to each other are displayed as corresponding negative and positive regions in the SR plot. The nonparametric DIVA test is designed for connecting SR to discriminatory ability of a variable quantified as probability for correct classification. A mean probability for a certain SR range is calculated as the mean correct classification rate (MCCR) for all variables in the same SR interval. The MCCR is thus similar to a mean sensitivity in each SR interval. In addition to the ranking of all variables according to their discriminatory ability provided by the SR plot, the DIVA test connects a probability measure to each SR interval. Thus, the DIVA test makes it possible to objectively define thresholds corresponding to mean probability levels in the SR plot and provides a quantitative means to select discriminating variables. In order to validate the approach, samples of untreated cerebrospinal fluid (CSF) and samples spiked with a multicomponent peptide standard were analyzed by matrix-assisted laser desorption ionization (MALDI) mass spectrometry. The differences in the multivariate spectral profiles of the two groups were revealed using partial least-squares discriminant analysis (PLS-DA) followed by target projection (TP). The most discriminating mass-to-charge (m/z) regions were revealed by calculating the ratio of explained to unexplained variance for each m/z number on the target-projected component and displaying this measure in SR plots with quantitative boundaries determined from the DIVA test. The results are compared to some established methods for variable selection.

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Year:  2009        PMID: 19228047     DOI: 10.1021/ac802514y

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  35 in total

1.  Simplify: A Mass Spectrometry Metabolomics Approach to Identify Additives and Synergists from Complex Mixtures.

Authors:  Lindsay K Caesar; Sabina Nogo; Cassandra N Naphen; Nadja B Cech
Journal:  Anal Chem       Date:  2019-08-15       Impact factor: 6.986

2.  Determination of Adulteration Content in Extra Virgin Olive Oil Using FT-NIR Spectroscopy Combined with the BOSS-PLS Algorithm.

Authors:  Hui Jiang; Quansheng Chen
Journal:  Molecules       Date:  2019-06-06       Impact factor: 4.411

3.  A 1H NMR metabolomic approach for the estimation of the time since death using aqueous humour: an animal model.

Authors:  Emanuela Locci; Matteo Stocchero; Antonio Noto; Alberto Chighine; Luca Natali; Pietro Emanuele Napoli; Roberto Caria; Fabio De-Giorgio; Matteo Nioi; Ernesto d'Aloja
Journal:  Metabolomics       Date:  2019-05-08       Impact factor: 4.290

4.  Orbitofrontal Neuroadaptations and Cross-Species Synaptic Biomarkers in Heavy-Drinking Macaques.

Authors:  Sudarat Nimitvilai; Joachim D Uys; John J Woodward; Patrick K Randall; Lauren E Ball; Robert W Williams; Byron C Jones; Lu Lu; Kathleen A Grant; Patrick J Mulholland
Journal:  J Neurosci       Date:  2017-03-07       Impact factor: 6.167

Review 5.  Synergy and antagonism in natural product extracts: when 1 + 1 does not equal 2.

Authors:  Lindsay K Caesar; Nadja B Cech
Journal:  Nat Prod Rep       Date:  2019-06-19       Impact factor: 13.423

6.  Opportunities and Limitations for Untargeted Mass Spectrometry Metabolomics to Identify Biologically Active Constituents in Complex Natural Product Mixtures.

Authors:  Lindsay K Caesar; Joshua J Kellogg; Olav M Kvalheim; Nadja B Cech
Journal:  J Nat Prod       Date:  2019-03-07       Impact factor: 4.050

7.  A comparison of methods for classifying clinical samples based on proteomics data: a case study for statistical and machine learning approaches.

Authors:  Dayle L Sampson; Tony J Parker; Zee Upton; Cameron P Hurst
Journal:  PLoS One       Date:  2011-09-28       Impact factor: 3.240

Review 8.  Metabolomics and genomics in natural products research: complementary tools for targeting new chemical entities.

Authors:  Lindsay K Caesar; Rana Montaser; Nancy P Keller; Neil L Kelleher
Journal:  Nat Prod Rep       Date:  2021-11-17       Impact factor: 13.423

Review 9.  Selection and characterization of botanical natural products for research studies: a NaPDI center recommended approach.

Authors:  Joshua J Kellogg; Mary F Paine; Jeannine S McCune; Nicholas H Oberlies; Nadja B Cech
Journal:  Nat Prod Rep       Date:  2019-08-14       Impact factor: 13.423

10.  Biochemometrics for Natural Products Research: Comparison of Data Analysis Approaches and Application to Identification of Bioactive Compounds.

Authors:  Joshua J Kellogg; Daniel A Todd; Joseph M Egan; Huzefa A Raja; Nicholas H Oberlies; Olav M Kvalheim; Nadja B Cech
Journal:  J Nat Prod       Date:  2016-02-03       Impact factor: 4.050

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