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mspecLINE: bridging knowledge of human disease with the proteome

BACKGROUND: Public proteomics databases such as PeptideAtlas contain peptides and proteins identified in mass spectrometry experiments. However, these databases lack information about human disease for researchers studying disease-related proteins. We have developed mspecLINE, a tool that combines k...

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Detalles Bibliográficos
Autores principales: Handcock, Jeremy, Deutsch, Eric W, Boyle, John
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845087/
https://www.ncbi.nlm.nih.gov/pubmed/20219133
http://dx.doi.org/10.1186/1755-8794-3-7
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author Handcock, Jeremy
Deutsch, Eric W
Boyle, John
author_facet Handcock, Jeremy
Deutsch, Eric W
Boyle, John
author_sort Handcock, Jeremy
collection PubMed
description BACKGROUND: Public proteomics databases such as PeptideAtlas contain peptides and proteins identified in mass spectrometry experiments. However, these databases lack information about human disease for researchers studying disease-related proteins. We have developed mspecLINE, a tool that combines knowledge about human disease in MEDLINE with empirical data about the detectable human proteome in PeptideAtlas. mspecLINE associates diseases with proteins by calculating the semantic distance between annotated terms from a controlled biomedical vocabulary. We used an established semantic distance measure that is based on the co-occurrence of disease and protein terms in the MEDLINE bibliographic database. RESULTS: The mspecLINE web application allows researchers to explore relationships between human diseases and parts of the proteome that are detectable using a mass spectrometer. Given a disease, the tool will display proteins and peptides from PeptideAtlas that may be associated with the disease. It will also display relevant literature from MEDLINE. Furthermore, mspecLINE allows researchers to select proteotypic peptides for specific protein targets in a mass spectrometry assay. CONCLUSIONS: Although mspecLINE applies an information retrieval technique to the MEDLINE database, it is distinct from previous MEDLINE query tools in that it combines the knowledge expressed in scientific literature with empirical proteomics data. The tool provides valuable information about candidate protein targets to researchers studying human disease and is freely available on a public web server.
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spelling pubmed-28450872010-03-26 mspecLINE: bridging knowledge of human disease with the proteome Handcock, Jeremy Deutsch, Eric W Boyle, John BMC Med Genomics Software BACKGROUND: Public proteomics databases such as PeptideAtlas contain peptides and proteins identified in mass spectrometry experiments. However, these databases lack information about human disease for researchers studying disease-related proteins. We have developed mspecLINE, a tool that combines knowledge about human disease in MEDLINE with empirical data about the detectable human proteome in PeptideAtlas. mspecLINE associates diseases with proteins by calculating the semantic distance between annotated terms from a controlled biomedical vocabulary. We used an established semantic distance measure that is based on the co-occurrence of disease and protein terms in the MEDLINE bibliographic database. RESULTS: The mspecLINE web application allows researchers to explore relationships between human diseases and parts of the proteome that are detectable using a mass spectrometer. Given a disease, the tool will display proteins and peptides from PeptideAtlas that may be associated with the disease. It will also display relevant literature from MEDLINE. Furthermore, mspecLINE allows researchers to select proteotypic peptides for specific protein targets in a mass spectrometry assay. CONCLUSIONS: Although mspecLINE applies an information retrieval technique to the MEDLINE database, it is distinct from previous MEDLINE query tools in that it combines the knowledge expressed in scientific literature with empirical proteomics data. The tool provides valuable information about candidate protein targets to researchers studying human disease and is freely available on a public web server. BioMed Central 2010-03-10 /pmc/articles/PMC2845087/ /pubmed/20219133 http://dx.doi.org/10.1186/1755-8794-3-7 Text en Copyright ©2010 Handcock et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Software
Handcock, Jeremy
Deutsch, Eric W
Boyle, John
mspecLINE: bridging knowledge of human disease with the proteome
title mspecLINE: bridging knowledge of human disease with the proteome
title_full mspecLINE: bridging knowledge of human disease with the proteome
title_fullStr mspecLINE: bridging knowledge of human disease with the proteome
title_full_unstemmed mspecLINE: bridging knowledge of human disease with the proteome
title_short mspecLINE: bridging knowledge of human disease with the proteome
title_sort mspecline: bridging knowledge of human disease with the proteome
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845087/
https://www.ncbi.nlm.nih.gov/pubmed/20219133
http://dx.doi.org/10.1186/1755-8794-3-7
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