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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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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/ |
format | Online Article Text |
id | pubmed-4897594 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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