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Statistical methods for quantitative mass spectrometry proteomic experiments with labeling

Mass Spectrometry utilizing labeling allows multiple specimens to be subjected to mass spectrometry simultaneously. As a result, between-experiment variability is reduced. Here we describe use of fundamental concepts of statistical experimental design in the labeling framework in order to minimize v...

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Detalles Bibliográficos
Autores principales: Oberg, Ann L, Mahoney, Douglas W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3489540/
https://www.ncbi.nlm.nih.gov/pubmed/23176383
http://dx.doi.org/10.1186/1471-2105-13-S16-S7
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author Oberg, Ann L
Mahoney, Douglas W
author_facet Oberg, Ann L
Mahoney, Douglas W
author_sort Oberg, Ann L
collection PubMed
description Mass Spectrometry utilizing labeling allows multiple specimens to be subjected to mass spectrometry simultaneously. As a result, between-experiment variability is reduced. Here we describe use of fundamental concepts of statistical experimental design in the labeling framework in order to minimize variability and avoid biases. We demonstrate how to export data in the format that is most efficient for statistical analysis. We demonstrate how to assess the need for normalization, perform normalization, and check whether it worked. We describe how to build a model explaining the observed values and test for differential protein abundance along with descriptive statistics and measures of reliability of the findings. Concepts are illustrated through the use of three case studies utilizing the iTRAQ 4-plex labeling protocol.
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spelling pubmed-34895402012-11-08 Statistical methods for quantitative mass spectrometry proteomic experiments with labeling Oberg, Ann L Mahoney, Douglas W BMC Bioinformatics Review Mass Spectrometry utilizing labeling allows multiple specimens to be subjected to mass spectrometry simultaneously. As a result, between-experiment variability is reduced. Here we describe use of fundamental concepts of statistical experimental design in the labeling framework in order to minimize variability and avoid biases. We demonstrate how to export data in the format that is most efficient for statistical analysis. We demonstrate how to assess the need for normalization, perform normalization, and check whether it worked. We describe how to build a model explaining the observed values and test for differential protein abundance along with descriptive statistics and measures of reliability of the findings. Concepts are illustrated through the use of three case studies utilizing the iTRAQ 4-plex labeling protocol. BioMed Central 2012-11-05 /pmc/articles/PMC3489540/ /pubmed/23176383 http://dx.doi.org/10.1186/1471-2105-13-S16-S7 Text en Copyright ©2012 Oberg and Mahoney; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Oberg, Ann L
Mahoney, Douglas W
Statistical methods for quantitative mass spectrometry proteomic experiments with labeling
title Statistical methods for quantitative mass spectrometry proteomic experiments with labeling
title_full Statistical methods for quantitative mass spectrometry proteomic experiments with labeling
title_fullStr Statistical methods for quantitative mass spectrometry proteomic experiments with labeling
title_full_unstemmed Statistical methods for quantitative mass spectrometry proteomic experiments with labeling
title_short Statistical methods for quantitative mass spectrometry proteomic experiments with labeling
title_sort statistical methods for quantitative mass spectrometry proteomic experiments with labeling
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3489540/
https://www.ncbi.nlm.nih.gov/pubmed/23176383
http://dx.doi.org/10.1186/1471-2105-13-S16-S7
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