The information bottleneck (IB) principle has been proven effective in various NLP applications. The existing work, however, only used either generative or information compression models to improve the performance of the target task. In this paper, we propose to combine the two types of IB models into one system to enhance Named Entity Recognition (NER).For one type of IB model, we incorporate two unsupervised generative components, span reconstruction and synonym generation, into a span-based NER system. The span reconstruction ensures that the contextualised span representation keeps the span information, while the synonym generation makes synonyms have similar representations even in different contexts. For the other type of IB model, we add a supervised IB layer that performs information compression into the system to preserve useful features for NER in the resulting span representations. Experiments on five different corpora indicate that jointly training both generative and information compression models can enhance the performance of the baseline span-based NER system. Our source code is publicly available at https://github.com/nguyennth/joint-ib-models.

Existing biomedical coreference resolution systems depend on features and/or rules based on syntactic parsers. In this paper, we investigate the utility of the state-of-the-art general domain neural coreference resolution system on biomedical texts. The system is an end-to-end system without depending on any syntactic parsers. We also investigate the domain specific features to enhance the system for biomedical texts. Experimental results on the BioNLP Protein Coreference dataset and the CRAFT corpus show that, with no parser information, the adapted system compared favorably with the systems that depend on parser information on these datasets, achieving 51.23% on the BioNLP dataset and 36.33% on the CRAFT corpus in F1 score. In-domain embeddings and domain-specific features helped improve the performance on the BioNLP dataset, but they did not on the CRAFT corpus.