Literature DB >> 19731396

NMR metabolic analysis of samples using fuzzy K-means clustering.

Miroslava Cuperlović-Culf1, Nabil Belacel, Adrian S Culf, Ian C Chute, Rodney J Ouellette, Ian W Burton, Tobias K Karakach, John A Walter.   

Abstract

The global analysis of metabolites can be used to define the phenotypes of cells, tissues or organisms. Classifying groups of samples based on their metabolic profile is one of the main topics of metabolomics research. Crisp clustering methods assign each feature to one cluster, thereby omitting information about the multiplicity of sample subtypes. Here, we present the application of fuzzy K-means clustering method for the classification of samples based on metabolomics 1D (1)H NMR fingerprints. The sample classification was performed on NMR spectra of cancer cell line extracts and of urine samples of type 2 diabetes patients and animal models. The cell line dataset included NMR spectra of lipophilic cell extracts for two normal and three cancer cell lines with cancer cell lines including two invasive and one non-invasive cancers. The second dataset included previously published NMR spectra of urine samples of human type 2 diabetics and healthy controls, mouse wild type and diabetes model and rat obese and lean phenotypes. The fuzzy K-means clustering method allowed more accurate sample classification in both datasets relative to the other tested methods including principal component analysis (PCA), hierarchical clustering (HCL) and K-means clustering. In the cell line samples, fuzzy clustering provided a clear separation of individual cell lines, groups of cancer and normal cell lines as well as non-invasive and invasive tumour cell lines. In the diabetes dataset, clear separation of healthy controls and diabetics in all three models was possible only by using the fuzzy clustering method.

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Year:  2009        PMID: 19731396     DOI: 10.1002/mrc.2502

Source DB:  PubMed          Journal:  Magn Reson Chem        ISSN: 0749-1581            Impact factor:   2.447


  7 in total

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2.  Navigating the human metabolome for biomarker identification and design of pharmaceutical molecules.

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3.  Quantification and statistical significance analysis of group separation in NMR-based metabonomics studies.

Authors:  Aaron M Goodpaster; Michael A Kennedy
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5.  Bioinformatics Tools for Mass Spectroscopy-Based Metabolomic Data Processing and Analysis.

Authors:  Masahiro Sugimoto; Masato Kawakami; Martin Robert; Tomoyoshi Soga; Masaru Tomita
Journal:  Curr Bioinform       Date:  2012-03       Impact factor: 3.543

6.  Identifying diseases-related metabolites using random walk.

Authors:  Yang Hu; Tianyi Zhao; Ningyi Zhang; Tianyi Zang; Jun Zhang; Liang Cheng
Journal:  BMC Bioinformatics       Date:  2018-04-11       Impact factor: 3.169

7.  Statistical HOmogeneous Cluster SpectroscopY (SHOCSY): an optimized statistical approach for clustering of ¹H NMR spectral data to reduce interference and enhance robust biomarkers selection.

Authors:  Xin Zou; Elaine Holmes; Jeremy K Nicholson; Ruey Leng Loo
Journal:  Anal Chem       Date:  2014-05-13       Impact factor: 6.986

  7 in total

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