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CoMAGC: a corpus with multi-faceted annotations of gene-cancer relations

BACKGROUND: In order to access the large amount of information in biomedical literature about genes implicated in various cancers both efficiently and accurately, the aid of text mining (TM) systems is invaluable. Current TM systems do target either gene-cancer relations or biological processes invo...

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Autores principales: Lee, Hee-Jin, Shim, Sang-Hyung, Song, Mi-Ryoung, Lee, Hyunju, Park, Jong C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833657/
https://www.ncbi.nlm.nih.gov/pubmed/24225062
http://dx.doi.org/10.1186/1471-2105-14-323
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author Lee, Hee-Jin
Shim, Sang-Hyung
Song, Mi-Ryoung
Lee, Hyunju
Park, Jong C
author_facet Lee, Hee-Jin
Shim, Sang-Hyung
Song, Mi-Ryoung
Lee, Hyunju
Park, Jong C
author_sort Lee, Hee-Jin
collection PubMed
description BACKGROUND: In order to access the large amount of information in biomedical literature about genes implicated in various cancers both efficiently and accurately, the aid of text mining (TM) systems is invaluable. Current TM systems do target either gene-cancer relations or biological processes involving genes and cancers, but the former type produces information not comprehensive enough to explain how a gene affects a cancer, and the latter does not provide a concise summary of gene-cancer relations. RESULTS: In this paper, we present a corpus for the development of TM systems that are specifically targeting gene-cancer relations but are still able to capture complex information in biomedical sentences. We describe CoMAGC, a corpus with multi-faceted annotations of gene-cancer relations. In CoMAGC, a piece of annotation is composed of four semantically orthogonal concepts that together express 1) how a gene changes, 2) how a cancer changes and 3) the causality between the gene and the cancer. The multi-faceted annotations are shown to have high inter-annotator agreement. In addition, we show that the annotations in CoMAGC allow us to infer the prospective roles of genes in cancers and to classify the genes into three classes according to the inferred roles. We encode the mapping between multi-faceted annotations and gene classes into 10 inference rules. The inference rules produce results with high accuracy as measured against human annotations. CoMAGC consists of 821 sentences on prostate, breast and ovarian cancers. Currently, we deal with changes in gene expression levels among other types of gene changes. The corpus is available at http://biopathway.org/CoMAGCunder the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0). CONCLUSIONS: The corpus will be an important resource for the development of advanced TM systems on gene-cancer relations.
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spelling pubmed-38336572013-11-20 CoMAGC: a corpus with multi-faceted annotations of gene-cancer relations Lee, Hee-Jin Shim, Sang-Hyung Song, Mi-Ryoung Lee, Hyunju Park, Jong C BMC Bioinformatics Research Article BACKGROUND: In order to access the large amount of information in biomedical literature about genes implicated in various cancers both efficiently and accurately, the aid of text mining (TM) systems is invaluable. Current TM systems do target either gene-cancer relations or biological processes involving genes and cancers, but the former type produces information not comprehensive enough to explain how a gene affects a cancer, and the latter does not provide a concise summary of gene-cancer relations. RESULTS: In this paper, we present a corpus for the development of TM systems that are specifically targeting gene-cancer relations but are still able to capture complex information in biomedical sentences. We describe CoMAGC, a corpus with multi-faceted annotations of gene-cancer relations. In CoMAGC, a piece of annotation is composed of four semantically orthogonal concepts that together express 1) how a gene changes, 2) how a cancer changes and 3) the causality between the gene and the cancer. The multi-faceted annotations are shown to have high inter-annotator agreement. In addition, we show that the annotations in CoMAGC allow us to infer the prospective roles of genes in cancers and to classify the genes into three classes according to the inferred roles. We encode the mapping between multi-faceted annotations and gene classes into 10 inference rules. The inference rules produce results with high accuracy as measured against human annotations. CoMAGC consists of 821 sentences on prostate, breast and ovarian cancers. Currently, we deal with changes in gene expression levels among other types of gene changes. The corpus is available at http://biopathway.org/CoMAGCunder the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0). CONCLUSIONS: The corpus will be an important resource for the development of advanced TM systems on gene-cancer relations. BioMed Central 2013-11-14 /pmc/articles/PMC3833657/ /pubmed/24225062 http://dx.doi.org/10.1186/1471-2105-14-323 Text en Copyright © 2013 Lee 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 Research Article
Lee, Hee-Jin
Shim, Sang-Hyung
Song, Mi-Ryoung
Lee, Hyunju
Park, Jong C
CoMAGC: a corpus with multi-faceted annotations of gene-cancer relations
title CoMAGC: a corpus with multi-faceted annotations of gene-cancer relations
title_full CoMAGC: a corpus with multi-faceted annotations of gene-cancer relations
title_fullStr CoMAGC: a corpus with multi-faceted annotations of gene-cancer relations
title_full_unstemmed CoMAGC: a corpus with multi-faceted annotations of gene-cancer relations
title_short CoMAGC: a corpus with multi-faceted annotations of gene-cancer relations
title_sort comagc: a corpus with multi-faceted annotations of gene-cancer relations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833657/
https://www.ncbi.nlm.nih.gov/pubmed/24225062
http://dx.doi.org/10.1186/1471-2105-14-323
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