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Mining clinical attributes of genomic variants through assisted literature curation in Egas

The veritable deluge of biological data over recent years has led to the establishment of a considerable number of knowledge resources that compile curated information extracted from the literature and store it in structured form, facilitating its use and exploitation. In this article, we focus on t...

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Detalles Bibliográficos
Autores principales: Matos, Sérgio, Campos, David, Pinho, Renato, Silva, Raquel M., Mort, Matthew, Cooper, David N., Oliveira, José Luís
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897594/
https://www.ncbi.nlm.nih.gov/pubmed/27278817
http://dx.doi.org/10.1093/database/baw096
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author Matos, Sérgio
Campos, David
Pinho, Renato
Silva, Raquel M.
Mort, Matthew
Cooper, David N.
Oliveira, José Luís
author_facet Matos, Sérgio
Campos, David
Pinho, Renato
Silva, Raquel M.
Mort, Matthew
Cooper, David N.
Oliveira, José Luís
author_sort Matos, Sérgio
collection PubMed
description The veritable deluge of biological data over recent years has led to the establishment of a considerable number of knowledge resources that compile curated information extracted from the literature and store it in structured form, facilitating its use and exploitation. In this article, we focus on the curation of inherited genetic variants and associated clinical attributes, such as zygosity, penetrance or inheritance mode, and describe the use of Egas for this task. Egas is a web-based platform for text-mining assisted literature curation that focuses on usability through modern design solutions and simple user interactions. Egas offers a flexible and customizable tool that allows defining the concept types and relations of interest for a given annotation task, as well as the ontologies used for normalizing each concept type. Further, annotations may be performed on raw documents or on the results of automated concept identification and relation extraction tools. Users can inspect, correct or remove automatic text-mining results, manually add new annotations, and export the results to standard formats. Egas is compatible with the most recent versions of Google Chrome, Mozilla Firefox, Internet Explorer and Safari and is available for use at https://demo.bmd-software.com/egas/. Database URL: https://demo.bmd-software.com/egas/
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spelling pubmed-48975942016-06-10 Mining clinical attributes of genomic variants through assisted literature curation in Egas Matos, Sérgio Campos, David Pinho, Renato Silva, Raquel M. Mort, Matthew Cooper, David N. Oliveira, José Luís Database (Oxford) Original Article The veritable deluge of biological data over recent years has led to the establishment of a considerable number of knowledge resources that compile curated information extracted from the literature and store it in structured form, facilitating its use and exploitation. In this article, we focus on the curation of inherited genetic variants and associated clinical attributes, such as zygosity, penetrance or inheritance mode, and describe the use of Egas for this task. Egas is a web-based platform for text-mining assisted literature curation that focuses on usability through modern design solutions and simple user interactions. Egas offers a flexible and customizable tool that allows defining the concept types and relations of interest for a given annotation task, as well as the ontologies used for normalizing each concept type. Further, annotations may be performed on raw documents or on the results of automated concept identification and relation extraction tools. Users can inspect, correct or remove automatic text-mining results, manually add new annotations, and export the results to standard formats. Egas is compatible with the most recent versions of Google Chrome, Mozilla Firefox, Internet Explorer and Safari and is available for use at https://demo.bmd-software.com/egas/. Database URL: https://demo.bmd-software.com/egas/ Oxford University Press 2016-06-07 /pmc/articles/PMC4897594/ /pubmed/27278817 http://dx.doi.org/10.1093/database/baw096 Text en © The Author(s) 2016. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Matos, Sérgio
Campos, David
Pinho, Renato
Silva, Raquel M.
Mort, Matthew
Cooper, David N.
Oliveira, José Luís
Mining clinical attributes of genomic variants through assisted literature curation in Egas
title Mining clinical attributes of genomic variants through assisted literature curation in Egas
title_full Mining clinical attributes of genomic variants through assisted literature curation in Egas
title_fullStr Mining clinical attributes of genomic variants through assisted literature curation in Egas
title_full_unstemmed Mining clinical attributes of genomic variants through assisted literature curation in Egas
title_short Mining clinical attributes of genomic variants through assisted literature curation in Egas
title_sort mining clinical attributes of genomic variants through assisted literature curation in egas
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897594/
https://www.ncbi.nlm.nih.gov/pubmed/27278817
http://dx.doi.org/10.1093/database/baw096
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