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Long short-term memory RNN for biomedical named entity recognition
BACKGROUND: Biomedical named entity recognition(BNER) is a crucial initial step of information extraction in biomedical domain. The task is typically modeled as a sequence labeling problem. Various machine learning algorithms, such as Conditional Random Fields (CRFs), have been successfully used for...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663060/ https://www.ncbi.nlm.nih.gov/pubmed/29084508 http://dx.doi.org/10.1186/s12859-017-1868-5 |
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author | Lyu, Chen Chen, Bo Ren, Yafeng Ji, Donghong |
author_facet | Lyu, Chen Chen, Bo Ren, Yafeng Ji, Donghong |
author_sort | Lyu, Chen |
collection | PubMed |
description | BACKGROUND: Biomedical named entity recognition(BNER) is a crucial initial step of information extraction in biomedical domain. The task is typically modeled as a sequence labeling problem. Various machine learning algorithms, such as Conditional Random Fields (CRFs), have been successfully used for this task. However, these state-of-the-art BNER systems largely depend on hand-crafted features. RESULTS: We present a recurrent neural network (RNN) framework based on word embeddings and character representation. On top of the neural network architecture, we use a CRF layer to jointly decode labels for the whole sentence. In our approach, contextual information from both directions and long-range dependencies in the sequence, which is useful for this task, can be well modeled by bidirectional variation and long short-term memory (LSTM) unit, respectively. Although our models use word embeddings and character embeddings as the only features, the bidirectional LSTM-RNN (BLSTM-RNN) model achieves state-of-the-art performance — 86.55% F1 on BioCreative II gene mention (GM) corpus and 73.79% F1 on JNLPBA 2004 corpus. CONCLUSIONS: Our neural network architecture can be successfully used for BNER without any manual feature engineering. Experimental results show that domain-specific pre-trained word embeddings and character-level representation can improve the performance of the LSTM-RNN models. On the GM corpus, we achieve comparable performance compared with other systems using complex hand-crafted features. Considering the JNLPBA corpus, our model achieves the best results, outperforming the previously top performing systems. The source code of our method is freely available under GPL at https://github.com/lvchen1989/BNER. |
format | Online Article Text |
id | pubmed-5663060 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56630602017-11-01 Long short-term memory RNN for biomedical named entity recognition Lyu, Chen Chen, Bo Ren, Yafeng Ji, Donghong BMC Bioinformatics Research Article BACKGROUND: Biomedical named entity recognition(BNER) is a crucial initial step of information extraction in biomedical domain. The task is typically modeled as a sequence labeling problem. Various machine learning algorithms, such as Conditional Random Fields (CRFs), have been successfully used for this task. However, these state-of-the-art BNER systems largely depend on hand-crafted features. RESULTS: We present a recurrent neural network (RNN) framework based on word embeddings and character representation. On top of the neural network architecture, we use a CRF layer to jointly decode labels for the whole sentence. In our approach, contextual information from both directions and long-range dependencies in the sequence, which is useful for this task, can be well modeled by bidirectional variation and long short-term memory (LSTM) unit, respectively. Although our models use word embeddings and character embeddings as the only features, the bidirectional LSTM-RNN (BLSTM-RNN) model achieves state-of-the-art performance — 86.55% F1 on BioCreative II gene mention (GM) corpus and 73.79% F1 on JNLPBA 2004 corpus. CONCLUSIONS: Our neural network architecture can be successfully used for BNER without any manual feature engineering. Experimental results show that domain-specific pre-trained word embeddings and character-level representation can improve the performance of the LSTM-RNN models. On the GM corpus, we achieve comparable performance compared with other systems using complex hand-crafted features. Considering the JNLPBA corpus, our model achieves the best results, outperforming the previously top performing systems. The source code of our method is freely available under GPL at https://github.com/lvchen1989/BNER. BioMed Central 2017-10-30 /pmc/articles/PMC5663060/ /pubmed/29084508 http://dx.doi.org/10.1186/s12859-017-1868-5 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Lyu, Chen Chen, Bo Ren, Yafeng Ji, Donghong Long short-term memory RNN for biomedical named entity recognition |
title | Long short-term memory RNN for biomedical named entity recognition |
title_full | Long short-term memory RNN for biomedical named entity recognition |
title_fullStr | Long short-term memory RNN for biomedical named entity recognition |
title_full_unstemmed | Long short-term memory RNN for biomedical named entity recognition |
title_short | Long short-term memory RNN for biomedical named entity recognition |
title_sort | long short-term memory rnn for biomedical named entity recognition |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663060/ https://www.ncbi.nlm.nih.gov/pubmed/29084508 http://dx.doi.org/10.1186/s12859-017-1868-5 |
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