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Signatures for Mass Spectrometry Data Quality
[Image: see text] Ensuring data quality and proper instrument functionality is a prerequisite for scientific investigation. Manual quality assurance is time-consuming and subjective. Metrics for describing liquid chromatography mass spectrometry (LC–MS) data have been developed; however, the wide va...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4104976/ https://www.ncbi.nlm.nih.gov/pubmed/24611607 http://dx.doi.org/10.1021/pr401143e |
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author | Amidan, Brett G. Orton, Daniel J. LaMarche, Brian L. Monroe, Matthew E. Moore, Ronald J. Venzin, Alexander M. Smith, Richard D. Sego, Landon H. Tardiff, Mark F. Payne, Samuel H. |
author_facet | Amidan, Brett G. Orton, Daniel J. LaMarche, Brian L. Monroe, Matthew E. Moore, Ronald J. Venzin, Alexander M. Smith, Richard D. Sego, Landon H. Tardiff, Mark F. Payne, Samuel H. |
author_sort | Amidan, Brett G. |
collection | PubMed |
description | [Image: see text] Ensuring data quality and proper instrument functionality is a prerequisite for scientific investigation. Manual quality assurance is time-consuming and subjective. Metrics for describing liquid chromatography mass spectrometry (LC–MS) data have been developed; however, the wide variety of LC–MS instruments and configurations precludes applying a simple cutoff. Using 1150 manually classified quality control (QC) data sets, we trained logistic regression classification models to predict whether a data set is in or out of control. Model parameters were optimized by minimizing a loss function that accounts for the trade-off between false positive and false negative errors. The classifier models detected bad data sets with high sensitivity while maintaining high specificity. Moreover, the composite classifier was dramatically more specific than single metrics. Finally, we evaluated the performance of the classifier on a separate validation set where it performed comparably to the results for the testing/training data sets. By presenting the methods and software used to create the classifier, other groups can create a classifier for their specific QC regimen, which is highly variable lab-to-lab. In total, this manuscript presents 3400 LC–MS data sets for the same QC sample (whole cell lysate of Shewanella oneidensis), deposited to the ProteomeXchange with identifiers PXD000320–PXD000324. |
format | Online Article Text |
id | pubmed-4104976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-41049762014-07-21 Signatures for Mass Spectrometry Data Quality Amidan, Brett G. Orton, Daniel J. LaMarche, Brian L. Monroe, Matthew E. Moore, Ronald J. Venzin, Alexander M. Smith, Richard D. Sego, Landon H. Tardiff, Mark F. Payne, Samuel H. J Proteome Res [Image: see text] Ensuring data quality and proper instrument functionality is a prerequisite for scientific investigation. Manual quality assurance is time-consuming and subjective. Metrics for describing liquid chromatography mass spectrometry (LC–MS) data have been developed; however, the wide variety of LC–MS instruments and configurations precludes applying a simple cutoff. Using 1150 manually classified quality control (QC) data sets, we trained logistic regression classification models to predict whether a data set is in or out of control. Model parameters were optimized by minimizing a loss function that accounts for the trade-off between false positive and false negative errors. The classifier models detected bad data sets with high sensitivity while maintaining high specificity. Moreover, the composite classifier was dramatically more specific than single metrics. Finally, we evaluated the performance of the classifier on a separate validation set where it performed comparably to the results for the testing/training data sets. By presenting the methods and software used to create the classifier, other groups can create a classifier for their specific QC regimen, which is highly variable lab-to-lab. In total, this manuscript presents 3400 LC–MS data sets for the same QC sample (whole cell lysate of Shewanella oneidensis), deposited to the ProteomeXchange with identifiers PXD000320–PXD000324. American Chemical Society 2014-03-10 2014-04-04 /pmc/articles/PMC4104976/ /pubmed/24611607 http://dx.doi.org/10.1021/pr401143e Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Amidan, Brett G. Orton, Daniel J. LaMarche, Brian L. Monroe, Matthew E. Moore, Ronald J. Venzin, Alexander M. Smith, Richard D. Sego, Landon H. Tardiff, Mark F. Payne, Samuel H. Signatures for Mass Spectrometry Data Quality |
title | Signatures for Mass Spectrometry
Data Quality |
title_full | Signatures for Mass Spectrometry
Data Quality |
title_fullStr | Signatures for Mass Spectrometry
Data Quality |
title_full_unstemmed | Signatures for Mass Spectrometry
Data Quality |
title_short | Signatures for Mass Spectrometry
Data Quality |
title_sort | signatures for mass spectrometry
data quality |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4104976/ https://www.ncbi.nlm.nih.gov/pubmed/24611607 http://dx.doi.org/10.1021/pr401143e |
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