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Pipasic: similarity and expression correction for strain-level identification and quantification in metaproteomics
Motivation: Metaproteomic analysis allows studying the interplay of organisms or functional groups and has become increasingly popular also for diagnostic purposes. However, difficulties arise owing to the high sequence similarity between related organisms. Further, the state of conservation of prot...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058918/ https://www.ncbi.nlm.nih.gov/pubmed/24931978 http://dx.doi.org/10.1093/bioinformatics/btu267 |
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author | Penzlin, Anke Lindner, Martin S. Doellinger, Joerg Dabrowski, Piotr Wojtek Nitsche, Andreas Renard, Bernhard Y. |
author_facet | Penzlin, Anke Lindner, Martin S. Doellinger, Joerg Dabrowski, Piotr Wojtek Nitsche, Andreas Renard, Bernhard Y. |
author_sort | Penzlin, Anke |
collection | PubMed |
description | Motivation: Metaproteomic analysis allows studying the interplay of organisms or functional groups and has become increasingly popular also for diagnostic purposes. However, difficulties arise owing to the high sequence similarity between related organisms. Further, the state of conservation of proteins between species can be correlated with their expression level, which can lead to significant bias in results and interpretation. These challenges are similar but not identical to the challenges arising in the analysis of metagenomic samples and require specific solutions. Results: We introduce Pipasic (peptide intensity-weighted proteome abundance similarity correction) as a tool that corrects identification and spectral counting-based quantification results using peptide similarity estimation and expression level weighting within a non-negative lasso framework. Pipasic has distinct advantages over approaches only regarding unique peptides or aggregating results to the lowest common ancestor, as demonstrated on examples of viral diagnostics and an acid mine drainage dataset. Availability and implementation: Pipasic source code is freely available from https://sourceforge.net/projects/pipasic/. Contact: RenardB@rki.de Supplementary information: Supplementary data are available at Bioinformatics online |
format | Online Article Text |
id | pubmed-4058918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40589182014-06-18 Pipasic: similarity and expression correction for strain-level identification and quantification in metaproteomics Penzlin, Anke Lindner, Martin S. Doellinger, Joerg Dabrowski, Piotr Wojtek Nitsche, Andreas Renard, Bernhard Y. Bioinformatics Ismb 2014 Proceedings Papers Committee Motivation: Metaproteomic analysis allows studying the interplay of organisms or functional groups and has become increasingly popular also for diagnostic purposes. However, difficulties arise owing to the high sequence similarity between related organisms. Further, the state of conservation of proteins between species can be correlated with their expression level, which can lead to significant bias in results and interpretation. These challenges are similar but not identical to the challenges arising in the analysis of metagenomic samples and require specific solutions. Results: We introduce Pipasic (peptide intensity-weighted proteome abundance similarity correction) as a tool that corrects identification and spectral counting-based quantification results using peptide similarity estimation and expression level weighting within a non-negative lasso framework. Pipasic has distinct advantages over approaches only regarding unique peptides or aggregating results to the lowest common ancestor, as demonstrated on examples of viral diagnostics and an acid mine drainage dataset. Availability and implementation: Pipasic source code is freely available from https://sourceforge.net/projects/pipasic/. Contact: RenardB@rki.de Supplementary information: Supplementary data are available at Bioinformatics online Oxford University Press 2014-06-15 2014-06-11 /pmc/articles/PMC4058918/ /pubmed/24931978 http://dx.doi.org/10.1093/bioinformatics/btu267 Text en © The Author 2014. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Ismb 2014 Proceedings Papers Committee Penzlin, Anke Lindner, Martin S. Doellinger, Joerg Dabrowski, Piotr Wojtek Nitsche, Andreas Renard, Bernhard Y. Pipasic: similarity and expression correction for strain-level identification and quantification in metaproteomics |
title | Pipasic: similarity and expression correction for strain-level identification and quantification in metaproteomics |
title_full | Pipasic: similarity and expression correction for strain-level identification and quantification in metaproteomics |
title_fullStr | Pipasic: similarity and expression correction for strain-level identification and quantification in metaproteomics |
title_full_unstemmed | Pipasic: similarity and expression correction for strain-level identification and quantification in metaproteomics |
title_short | Pipasic: similarity and expression correction for strain-level identification and quantification in metaproteomics |
title_sort | pipasic: similarity and expression correction for strain-level identification and quantification in metaproteomics |
topic | Ismb 2014 Proceedings Papers Committee |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058918/ https://www.ncbi.nlm.nih.gov/pubmed/24931978 http://dx.doi.org/10.1093/bioinformatics/btu267 |
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