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A new estimation of protein-level false discovery rate

BACKGROUND: In mass spectrometry-based proteomics, protein identification is an essential task. Evaluating the statistical significance of the protein identification result is critical to the success of proteomics studies. Controlling the false discovery rate (FDR) is the most common method for assu...

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Autores principales: Wu, Guanying, Wan, Xiang, Xu, Baohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6101079/
https://www.ncbi.nlm.nih.gov/pubmed/30367581
http://dx.doi.org/10.1186/s12864-018-4923-3
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author Wu, Guanying
Wan, Xiang
Xu, Baohua
author_facet Wu, Guanying
Wan, Xiang
Xu, Baohua
author_sort Wu, Guanying
collection PubMed
description BACKGROUND: In mass spectrometry-based proteomics, protein identification is an essential task. Evaluating the statistical significance of the protein identification result is critical to the success of proteomics studies. Controlling the false discovery rate (FDR) is the most common method for assuring the overall quality of the set of identifications. Existing FDR estimation methods either rely on specific assumptions or rely on the two-stage calculation process of first estimating the error rates at the peptide-level, and then combining them somehow at the protein-level. We propose to estimate the FDR in a non-parametric way with less assumptions and to avoid the two-stage calculation process. RESULTS: We propose a new protein-level FDR estimation framework. The framework contains two major components: the Permutation+BH (Benjamini–Hochberg) FDR estimation method and the logistic regression-based null inference method. In Permutation+BH, the null distribution of a sample is generated by searching data against a large number of permuted random protein database and therefore does not rely on specific assumptions. Then, p-values of proteins are calculated from the null distribution and the BH procedure is applied to the p-values to achieve the relationship of the FDR and the number of protein identifications. The Permutation+BH method generates the null distribution by the permutation method, which is inefficient for online identification. The logistic regression model is proposed to infer the null distribution of a new sample based on existing null distributions obtained from the Permutation+BH method. CONCLUSIONS: In our experiment based on three public available datasets, our Permutation+BH method achieves consistently better performance than MAYU, which is chosen as the benchmark FDR calculation method for this study. The null distribution inference result shows that the logistic regression model achieves a reasonable result both in the shape of the null distribution and the corresponding FDR estimation result.
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spelling pubmed-61010792018-08-27 A new estimation of protein-level false discovery rate Wu, Guanying Wan, Xiang Xu, Baohua BMC Genomics Research BACKGROUND: In mass spectrometry-based proteomics, protein identification is an essential task. Evaluating the statistical significance of the protein identification result is critical to the success of proteomics studies. Controlling the false discovery rate (FDR) is the most common method for assuring the overall quality of the set of identifications. Existing FDR estimation methods either rely on specific assumptions or rely on the two-stage calculation process of first estimating the error rates at the peptide-level, and then combining them somehow at the protein-level. We propose to estimate the FDR in a non-parametric way with less assumptions and to avoid the two-stage calculation process. RESULTS: We propose a new protein-level FDR estimation framework. The framework contains two major components: the Permutation+BH (Benjamini–Hochberg) FDR estimation method and the logistic regression-based null inference method. In Permutation+BH, the null distribution of a sample is generated by searching data against a large number of permuted random protein database and therefore does not rely on specific assumptions. Then, p-values of proteins are calculated from the null distribution and the BH procedure is applied to the p-values to achieve the relationship of the FDR and the number of protein identifications. The Permutation+BH method generates the null distribution by the permutation method, which is inefficient for online identification. The logistic regression model is proposed to infer the null distribution of a new sample based on existing null distributions obtained from the Permutation+BH method. CONCLUSIONS: In our experiment based on three public available datasets, our Permutation+BH method achieves consistently better performance than MAYU, which is chosen as the benchmark FDR calculation method for this study. The null distribution inference result shows that the logistic regression model achieves a reasonable result both in the shape of the null distribution and the corresponding FDR estimation result. BioMed Central 2018-08-13 /pmc/articles/PMC6101079/ /pubmed/30367581 http://dx.doi.org/10.1186/s12864-018-4923-3 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wu, Guanying
Wan, Xiang
Xu, Baohua
A new estimation of protein-level false discovery rate
title A new estimation of protein-level false discovery rate
title_full A new estimation of protein-level false discovery rate
title_fullStr A new estimation of protein-level false discovery rate
title_full_unstemmed A new estimation of protein-level false discovery rate
title_short A new estimation of protein-level false discovery rate
title_sort new estimation of protein-level false discovery rate
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6101079/
https://www.ncbi.nlm.nih.gov/pubmed/30367581
http://dx.doi.org/10.1186/s12864-018-4923-3
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