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New methods to identify high peak density artifacts in Fourier transform mass spectra and to mitigate their effects on high-throughput metabolomic data analysis.
Mitchell, Joshua M; Flight, Robert M; Wang, Qing Jun; Higashi, Richard M; Fan, Teresa W-M; Lane, Andrew N; Moseley, Hunter N B.
Afiliación
  • Mitchell JM; Department of Molecular & Cellular Biochemistry, University of Kentucky, Lexington, KY, USA.
  • Flight RM; Markey Cancer Center, University of Kentucky, Lexington, KY, USA.
  • Wang QJ; Center for Environment and Systems Biochemistry and the Resource Center for Stable Isotope Resolved Metabolomics, University of Kentucky, Lexington, KY, USA.
  • Higashi RM; Markey Cancer Center, University of Kentucky, Lexington, KY, USA.
  • Fan TW; Center for Environment and Systems Biochemistry and the Resource Center for Stable Isotope Resolved Metabolomics, University of Kentucky, Lexington, KY, USA.
  • Lane AN; Markey Cancer Center, University of Kentucky, Lexington, KY, USA.
  • Moseley HNB; Department of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, KY, USA.
Metabolomics ; 14(10): 125, 2018 09 17.
Article en En | MEDLINE | ID: mdl-30830442
ABSTRACT

INTRODUCTION:

Direct injection Fourier-transform mass spectrometry (FT-MS) allows for the high-throughput and high-resolution detection of thousands of metabolite-associated isotopologues. However, spectral artifacts can generate large numbers of spectral features (peaks) that do not correspond to known compounds. Misassignment of these artifactual features creates interpretive errors and limits our ability to discern the role of representative features within living systems.

OBJECTIVES:

Our goal is to develop rigorous methods that identify and handle spectral artifacts within the context of high-throughput FT-MS-based metabolomics studies.

RESULTS:

We observed three types of artifacts unique to FT-MS that we named high peak density (HPD) sites fuzzy sites, ringing and partial ringing. While ringing artifacts are well-known, fuzzy sites and partial ringing have not been previously well-characterized in the literature. We developed new computational methods based on comparisons of peak density within a spectrum to identify regions of spectra with fuzzy sites. We used these methods to identify and eliminate fuzzy site artifacts in an example dataset of paired cancer and non-cancer lung tissue samples and evaluated the impact of these artifacts on classification accuracy and robustness.

CONCLUSION:

Our methods robustly identified consistent fuzzy site artifacts in our FT-MS metabolomics spectral data. Without artifact identification and removal, 91.4% classification accuracy was achieved on an example lung cancer dataset; however, these classifiers rely heavily on artifactual features present in fuzzy sites. Proper removal of fuzzy site artifacts produces a more robust classifier based on non-artifactual features, with slightly improved accuracy of 92.4% in our example analysis.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Espectrometría de Masas / Carcinoma de Pulmón de Células no Pequeñas / Metabolómica / Ensayos Analíticos de Alto Rendimiento / Análisis de Fourier / Pulmón / Neoplasias Pulmonares Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Metabolomics Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Espectrometría de Masas / Carcinoma de Pulmón de Células no Pequeñas / Metabolómica / Ensayos Analíticos de Alto Rendimiento / Análisis de Fourier / Pulmón / Neoplasias Pulmonares Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Metabolomics Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos