Evidence map›Paper›PMID 21985394›Full record

ArticleBMC bioinformatics2011

An empirical Bayes model using a competition score for metabolite identification in gas chromatography mass spectrometry.

Jaesik Jeong, Xue Shi, Xiang Zhang, Seongho Kim, Changyu Shen

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In one paragraph

Article in BMC bioinformatics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Untargeted Metabolomics Strategies-Challenges and Emerging Directions.Journal of the American Society for Mass Spectrometry · 2016
    Review
  10. Article
  11. Article
  12. Article
  13. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Jaesik JeongDepartment of Biostatistics, Indiana University, 410 West 10th Street, Indianapolis, IN 46202, USA.
Xue Shi
Xiang Zhang
Seongho Kim
Changyu Shen

Funding

Mass Informatics of Two Dimensinoal Gas Chromatography Time-of-flight Mass SpectrR01GM087735 · NIGMS · UNIVERSITY OF LOUISVILLE · PI ZHANG, XIANG · 2009 to 2012
$1.4M
NIGMS NIH HHS 1R01GM087735NIGMS NIH HHS R01 GM087735
6 · The paper itself

Abstract

backgroundMass spectrometry (MS) based metabolite profiling has been increasingly popular for scientific and biomedical studies, primarily due to recent technological development such as comprehensive two-dimensional gas chromatography time-of-flight mass spectrometry (GCxGC/TOF-MS). Nevertheless, the identifications of metabolites from complex samples are subject to errors. Statistical/computational approaches to improve the accuracy of the identifications and false positive estimate are in great need. We propose an empirical Bayes model which accounts for a competing score in addition to the similarity score to tackle this problem. The competition score characterizes the propensity of a candidate metabolite of being matched to some spectrum based on the metabolite's similarity score with other spectra in the library searched against. The competition score allows the model to properly assess the evidence on the presence/absence status of a metabolite based on whether or not the metabolite is matched to some sample spectrum.

resultsWith a mixture of metabolite standards, we demonstrated that our method has better identification accuracy than other four existing methods. Moreover, our method has reliable false discovery rate estimate. We also applied our method to the data collected from the plasma of a rat and identified some metabolites from the plasma under the control of false discovery rate.

conclusionsWe developed an empirical Bayes model for metabolite identification and validated the method through a mixture of metabolite standards and rat plasma. The results show that our hierarchical model improves identification accuracy as compared with methods that do not structurally model the involved variables. The improvement in identification accuracy is likely to facilitate downstream analysis such as peak alignment and biomarker identification. Raw data and result matrices can be found at http://www.biostat.iupui.edu/~ChangyuShen/index.htm.

trial registration2123938128573429.

Indexed as

Bayes TheoremAnimalsFatty AcidsGas Chromatography-Mass SpectrometryPlasmaRatsFatty Acids

Identifiers

PMID21985394
PMCPMC3228553

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.