Background. Previous state-of-the-art systems on Drug Name Recognition (DNR) and Clinical Concept Extraction (CCE) have focused on a combination of text "feature engineering" and conventional machine learning algorithms such as conditional random fields and support vector machines. However, developing good features is inherently heavily time-consuming. Conversely, more modern machine learning approaches such as recurrent neural networks (RNNs) have proved capable of automatically learning effective features from either random assignments or automated word "embeddings". Objectives. (i) To create a highly accurate DNR and CCE system that avoids conventional, time-consuming feature engineering. (ii) To create richer, more specialized word embeddings by using health domain datasets such as MIMIC-III. (iii) To evaluate our systems over three contemporary datasets. Methods. Two deep learning methods, namely the Bidirectional LSTM and the Bidirectional LSTM-CRF, are evaluated. A CRF model is set as the baseline to compare the deep learning systems to a traditional machine learning approach. The same features are used for all the models. Results. We have obtained the best results with the Bidirectional LSTM-CRF model, which has outperformed all previously proposed systems. The specialized embeddings have helped to cover unusual words in DDI-DrugBank and DDI-MedLine, but not in the 2010 i2b2/VA IRB Revision dataset. Conclusion. We present a state-of-the-art system for DNR and CCE. Automated word embeddings has allowed us to avoid costly feature engineering and achieve higher accuracy. Nevertheless, the embeddings need to be retrained over datasets that are adequate for the domain, in order to adequately cover the domain-specific vocabulary.
Graphs possess a strong representational power for many types of patterns. However, a main limitation in their use for pattern analysis derives from their difficult mathematical treatment. One way of circumventing this problem is that of transforming the graphs into a vector space by means of graph embedding. Such an
Drug name recognition (DNR) is an essential step in the Pharmacovigilance (PV) pipeline. DNR aims to find drug name mentions in unstructured biomedical texts and classify them into predefined categories. State-of-the-art DNR approaches heavily rely on hand-crafted features and domain-specific resources which are difficult to collect and tune. For this reason, this paper investigates the effectiveness of contemporary recurrent neural architecturesthe Elman and Jordan networks and the bidirectional LSTM with CRF decoding -at performing DNR straight from the text. The experimental results achieved on the authoritative SemEval-2013 Task 9.1 benchmarks show that the bidirectional LSTM-CRF ranks closely to highly-dedicated, hand-crafted systems.
This paper proposes a novel graph-based method for representing a human's shape during the performance of an action. Despite their strong representational power, graphs are computationally cumbersome for pattern analysis. One way of circumventing this problem is that of transforming the graphs into a vector space by means of graph embedding. Such an embedding can be conveniently obtained by way of a set of "prototype" graphs and a dissimilarity measure: yet, the critical step in this approach is the selection of a suitable set of prototypes which can capture both the salient structure within each action class as well as the intra-class variation. This paper proposes a new discriminative approach for the selection of prototypes which maximizes a function of the inter-and intra-class distances. Experiments on an action recognition dataset reported in the paper show that such a discriminative approach outperforms well-established prototype selection methods such as center, border and random prototype selection.
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