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P4P: a peptidome-based strain-level genome comparison web tool
Peptidome similarity analysis enables researchers to gain insights into differential peptide profiles, providing a robust tool to discriminate strain-specific peptides, true intra-species differences among biological replicates or even microorganism-phenotype variations. However, no in silico peptid...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570244/ https://www.ncbi.nlm.nih.gov/pubmed/28482090 http://dx.doi.org/10.1093/nar/gkx389 |
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author | Blanco-Míguez, Aitor Fdez-Riverola, Florentino Lourenço, Anália Sánchez, Borja |
author_facet | Blanco-Míguez, Aitor Fdez-Riverola, Florentino Lourenço, Anália Sánchez, Borja |
author_sort | Blanco-Míguez, Aitor |
collection | PubMed |
description | Peptidome similarity analysis enables researchers to gain insights into differential peptide profiles, providing a robust tool to discriminate strain-specific peptides, true intra-species differences among biological replicates or even microorganism-phenotype variations. However, no in silico peptide fingerprinting software existed to facilitate such phylogeny inference. Hence, we developed the Peptidomes for Phylogenies (P4P) web tool, which enables the survey of similarities between microbial proteomes and simplifies the process of obtaining new biological insights into their phylogeny. P4P can be used to analyze different peptide datasets, i.e. bacteria, viruses, eukaryotic species or even metaproteomes. Also, it is able to work with whole proteome datasets and experimental mass-to-charge lists originated from mass spectrometers. The ultimate aim is to generate a valid and manageable list of peptides that have phylogenetic signal and are potentially sample-specific. Sample-to-sample comparison is based on a consensus peak set matrix, which can be further submitted to phylogenetic analysis. P4P holds great potential for improving phylogenetic analyses in challenging taxonomic groups, biomarker identification or epidemiologic studies. Notably, P4P can be of interest for applications handling large proteomic datasets, which it is able to reduce to small matrices while maintaining high phylogenetic resolution. The web server is available at http://sing-group.org/p4p. |
format | Online Article Text |
id | pubmed-5570244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55702442017-08-29 P4P: a peptidome-based strain-level genome comparison web tool Blanco-Míguez, Aitor Fdez-Riverola, Florentino Lourenço, Anália Sánchez, Borja Nucleic Acids Res Web Server Issue Peptidome similarity analysis enables researchers to gain insights into differential peptide profiles, providing a robust tool to discriminate strain-specific peptides, true intra-species differences among biological replicates or even microorganism-phenotype variations. However, no in silico peptide fingerprinting software existed to facilitate such phylogeny inference. Hence, we developed the Peptidomes for Phylogenies (P4P) web tool, which enables the survey of similarities between microbial proteomes and simplifies the process of obtaining new biological insights into their phylogeny. P4P can be used to analyze different peptide datasets, i.e. bacteria, viruses, eukaryotic species or even metaproteomes. Also, it is able to work with whole proteome datasets and experimental mass-to-charge lists originated from mass spectrometers. The ultimate aim is to generate a valid and manageable list of peptides that have phylogenetic signal and are potentially sample-specific. Sample-to-sample comparison is based on a consensus peak set matrix, which can be further submitted to phylogenetic analysis. P4P holds great potential for improving phylogenetic analyses in challenging taxonomic groups, biomarker identification or epidemiologic studies. Notably, P4P can be of interest for applications handling large proteomic datasets, which it is able to reduce to small matrices while maintaining high phylogenetic resolution. The web server is available at http://sing-group.org/p4p. Oxford University Press 2017-07-03 2017-05-08 /pmc/articles/PMC5570244/ /pubmed/28482090 http://dx.doi.org/10.1093/nar/gkx389 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), 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 | Web Server Issue Blanco-Míguez, Aitor Fdez-Riverola, Florentino Lourenço, Anália Sánchez, Borja P4P: a peptidome-based strain-level genome comparison web tool |
title | P4P: a peptidome-based strain-level genome comparison web tool |
title_full | P4P: a peptidome-based strain-level genome comparison web tool |
title_fullStr | P4P: a peptidome-based strain-level genome comparison web tool |
title_full_unstemmed | P4P: a peptidome-based strain-level genome comparison web tool |
title_short | P4P: a peptidome-based strain-level genome comparison web tool |
title_sort | p4p: a peptidome-based strain-level genome comparison web tool |
topic | Web Server Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570244/ https://www.ncbi.nlm.nih.gov/pubmed/28482090 http://dx.doi.org/10.1093/nar/gkx389 |
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