Evidence map›Paper›PMID 28810903›Full record

ArticleBMC bioinformatics2017

A neural network multi-task learning approach to biomedical named entity recognition.

Gamal Crichton, Sampo Pyysalo, Billy Chiu, Anna Korhonen

Abstract read
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Article in BMC bioinformatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

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43citing papers in PubMed
–field-weighted citation impact
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3 · Its place in the literature

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43 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Gamal CrichtonLanguage Technology Laboratory, DTAL, University of Cambridge, 9 West Road, Cambridge, CB39DB, UK. gkoc2@cam.ac.uk.ORCID http://orcid.org/0000-0002-3036-0811
Sampo PyysaloLanguage Technology Laboratory, DTAL, University of Cambridge, 9 West Road, Cambridge, CB39DB, UK.
Billy ChiuLanguage Technology Laboratory, DTAL, University of Cambridge, 9 West Road, Cambridge, CB39DB, UK.
Anna KorhonenLanguage Technology Laboratory, DTAL, University of Cambridge, 9 West Road, Cambridge, CB39DB, UK.

Funding

Medical Research Council MR/M013049/1
6 · The paper itself

Abstract

backgroundNamed Entity Recognition (NER) is a key task in biomedical text mining. Accurate NER systems require task-specific, manually-annotated datasets, which are expensive to develop and thus limited in size. Since such datasets contain related but different information, an interesting question is whether it might be possible to use them together to improve NER performance. To investigate this, we develop supervised, multi-task, convolutional neural network models and apply them to a large number of varied existing biomedical named entity datasets. Additionally, we investigated the effect of dataset size on performance in both single- and multi-task settings.

resultsWe present a single-task model for NER, a Multi-output multi-task model and a Dependent multi-task model. We apply the three models to 15 biomedical datasets containing multiple named entities including Anatomy, Chemical, Disease, Gene/Protein and Species. Each dataset represent a task. The results from the single-task model and the multi-task models are then compared for evidence of benefits from Multi-task Learning. With the Multi-output multi-task model we observed an average F-score improvement of 0.8% when compared to the single-task model from an average baseline of 78.4%. Although there was a significant drop in performance on one dataset, performance improves significantly for five datasets by up to 6.3%. For the Dependent multi-task model we observed an average improvement of 0.4% when compared to the single-task model. There were no significant drops in performance on any dataset, and performance improves significantly for six datasets by up to 1.1%. The dataset size experiments found that as dataset size decreased, the multi-output model's performance increased compared to the single-task model's. Using 50, 25 and 10% of the training data resulted in an average drop of approximately 3.4, 8 and 16.7% respectively for the single-task model but approximately 0.2, 3.0 and 9.8% for the multi-task model.

conclusionsOur results show that, on average, the multi-task models produced better NER results than the single-task models trained on a single NER dataset. We also found that Multi-task Learning is beneficial for small datasets. Across the various settings the improvements are significant, demonstrating the benefit of Multi-task Learning for this task.

Indexed as

Neural Networks, ComputerDatabases, FactualData MiningMachine LearningModels, TheoreticalBiomedical text miningConvolutional neural networksMulti-task learningNamed entity recognition

Identifiers

PMID28810903
PMCPMC5558737

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LicenceCC BY
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.