alexa A Statistical Technique for Monoisotopic Peak Detection
ISSN: 0974-276X

Journal of Proteomics & Bioinformatics
Open Access

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Research Article

A Statistical Technique for Monoisotopic Peak Detection in a Mass Spectrum

Mourad Atlas and Susmita Datta*

Department of Bioinformatics and Biostatistics School of Public Health and Information Science University of Louisville

*Corresponding Author:
Dr. S. Datta
Department of Bioinformatics and Biostatistics
School of Public Health and Information Science
University of Louisville
Tel: +01-502-8523294
Fax: +01-502-8523294
E-mail : [email protected]

Received Date: Mar 07, 2009; Accepted Date: April 30, 2009; Published Date: May 02, 2009

Citation: Atlas M, Datta S (2009) A Statistical Technique for Monoisotopic Peak Detection in a Mass Spectrum. J Proteomics Bioinform 2: 202-216. doi:10.4172/jpb.1000078

Copyright: © 2009 Atlas M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

Mass spectrometry has emerged as a core technology for high throughput proteomics profiling. It has enormous potential in biomedical research. However, the complexity of the data poses new statistical challenges for the analysis. Statistical methods and software developments for analyzing proteomic data are likely to continue to be a major area of research in the coming years. In this paper, a novel statistical method for analyzing high dimensional MALDI-TOF mass- spectrometry data in proteomic research is proposed. The chemical knowledge regarding isotopic distribution of the peptide molecules along with quantitative modeling is used to detect chemically valuable peaks from each spectrum. More specifically, a mixture of location-shifted Poisson distribution is fitted to the deamidated isotopic distribution of a peptide molecule. Maximum likelihood estimation by the expectation-maximization (EM) technique is used to estimate the parameters of the distribution. A formal statistical test is then constructed to determine whether a cluster of consecutive features (intensity values) in a mass spectrum corresponds to a true isotropic pattern. Thus, the monoisotopic peaks in an individual spectrum are identified. Performance of our method is examined through extensive simulations. We also provide a numerical illustration of our method with a real dataset and compare it with an existing method of peak detection. External biochemical validation of our detected peaks is provided.

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