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Evaluation of linear models and missing value imputation for the analysis of peptide-centric proteomics
BACKGROUND: Several methods to handle data generated from bottom-up proteomics via liquid chromatography-mass spectrometry, particularly for peptide-centric quantification dealing with post-translational modification (PTM) analysis like reversible cysteine oxidation are evaluated. The paper proposes...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419331/ https://www.ncbi.nlm.nih.gov/pubmed/30871482 http://dx.doi.org/10.1186/s12859-019-2619-6 |
_version_ | 1783403920191651840 |
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author | Berg, Philip McConnell, Evan W. Hicks, Leslie M. Popescu, Sorina C. Popescu, George V. |
author_facet | Berg, Philip McConnell, Evan W. Hicks, Leslie M. Popescu, Sorina C. Popescu, George V. |
author_sort | Berg, Philip |
collection | PubMed |
description | BACKGROUND: Several methods to handle data generated from bottom-up proteomics via liquid chromatography-mass spectrometry, particularly for peptide-centric quantification dealing with post-translational modification (PTM) analysis like reversible cysteine oxidation are evaluated. The paper proposes a pipeline based on the R programming language to analyze PTMs from peptide-centric label-free quantitative proteomics data. RESULTS: Our methodology includes variance stabilization, normalization, and missing data imputation to account for the large dynamic range of PTM measurements. It also corrects biases from an enrichment protocol and reduces the random and systematic errors associated with label-free quantification. The performance of the methodology is tested by performing proteome-wide differential PTM quantitation using linear models analysis (limma). We objectively compare two imputation methods along with significance testing when using multiple-imputation for missing data. CONCLUSION: Identifying PTMs in large-scale datasets is a problem with distinct characteristics that require new methods for handling missing data imputation and differential proteome analysis. Linear models in combination with multiple-imputation could significantly outperform a t-test-based decision method. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-019-2619-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6419331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64193312019-03-27 Evaluation of linear models and missing value imputation for the analysis of peptide-centric proteomics Berg, Philip McConnell, Evan W. Hicks, Leslie M. Popescu, Sorina C. Popescu, George V. BMC Bioinformatics Research BACKGROUND: Several methods to handle data generated from bottom-up proteomics via liquid chromatography-mass spectrometry, particularly for peptide-centric quantification dealing with post-translational modification (PTM) analysis like reversible cysteine oxidation are evaluated. The paper proposes a pipeline based on the R programming language to analyze PTMs from peptide-centric label-free quantitative proteomics data. RESULTS: Our methodology includes variance stabilization, normalization, and missing data imputation to account for the large dynamic range of PTM measurements. It also corrects biases from an enrichment protocol and reduces the random and systematic errors associated with label-free quantification. The performance of the methodology is tested by performing proteome-wide differential PTM quantitation using linear models analysis (limma). We objectively compare two imputation methods along with significance testing when using multiple-imputation for missing data. CONCLUSION: Identifying PTMs in large-scale datasets is a problem with distinct characteristics that require new methods for handling missing data imputation and differential proteome analysis. Linear models in combination with multiple-imputation could significantly outperform a t-test-based decision method. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-019-2619-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-03-14 /pmc/articles/PMC6419331/ /pubmed/30871482 http://dx.doi.org/10.1186/s12859-019-2619-6 Text en © The Author(s). 2019 Open AccessThis 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 Berg, Philip McConnell, Evan W. Hicks, Leslie M. Popescu, Sorina C. Popescu, George V. Evaluation of linear models and missing value imputation for the analysis of peptide-centric proteomics |
title | Evaluation of linear models and missing value imputation for the analysis of peptide-centric proteomics |
title_full | Evaluation of linear models and missing value imputation for the analysis of peptide-centric proteomics |
title_fullStr | Evaluation of linear models and missing value imputation for the analysis of peptide-centric proteomics |
title_full_unstemmed | Evaluation of linear models and missing value imputation for the analysis of peptide-centric proteomics |
title_short | Evaluation of linear models and missing value imputation for the analysis of peptide-centric proteomics |
title_sort | evaluation of linear models and missing value imputation for the analysis of peptide-centric proteomics |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419331/ https://www.ncbi.nlm.nih.gov/pubmed/30871482 http://dx.doi.org/10.1186/s12859-019-2619-6 |
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