Using Learning to Rank Approach to Promoting Diversity for Biomedical Information Retrieval with Wikipedia

In most of the traditional information retrieval (IR) models, the independent relevance assumption is taken, which assumes the relevance of a document is independent of other documents. However, the pitfall of this is the high redundancy and low diversity of retrieval result. This has been seen in many scenarios, especially in biomedical IR, where the information need of one query may refer to different aspects. Promoting diversity in IR takes the relationship between documents into account. Unlike previous studies, we tackle this problem in the learning to rank perspective. The main challenges are how to find salient features for biomedical data and how to integrate dynamic features into the ranking model. To address these challenges, Wikipedia is used to detect topics of documents for generating diversity biased features. A combined model is proposed and studied to learn a diversified ranking result. Experiment results show the proposed method outperforms baseline models

A neural autoencoder approach for document ranking and query refinement in pharmacogenomic information retrieval

In this study, we investigate learning-to- rank and query refinement approaches for information retrieval in the pharmacogenomic domain. The goal is to improve the information retrieval process of biomedical curators, who manually build knowledge bases for personalized medicine. We study how to exploit the relationships be- tween genes, variants, drugs, diseases and outcomes as features for document ranking and query refinement. For a supervised approach, we are faced with a small amount of annotated data and a large amount of unannotated data. Therefore, we explore ways to use a neural document auto-encoder in a semi-supervised approach. We show that a combination of established algorithms, feature-engineering and a neural auto-encoder model yield promising results in this setting

Bi-Encoders based Species Normalization -- Pairwise Sentence Learning to Rank

Motivation: Biomedical named-entity normalization involves connecting biomedical entities with distinct database identifiers in order to facilitate data integration across various fields of biology. Existing systems for biomedical named entity normalization heavily rely on dictionaries, manually created rules, and high-quality representative features such as lexical or morphological characteristics. However, recent research has investigated the use of neural network-based models to reduce dependence on dictionaries, manually crafted rules, and features. Despite these advancements, the performance of these models is still limited due to the lack of sufficiently large training datasets. These models have a tendency to overfit small training corpora and exhibit poor generalization when faced with previously unseen entities, necessitating the redesign of rules and features. Contribution: We present a novel deep learning approach for named entity normalization, treating it as a pair-wise learning to rank problem. Our method utilizes the widely-used information retrieval algorithm Best Matching 25 to generate candidate concepts, followed by the application of bi-directional encoder representation from the encoder (BERT) to re-rank the candidate list. Notably, our approach eliminates the need for feature-engineering or rule creation. We conduct experiments on species entity types and evaluate our method against state-of-the-art techniques using LINNAEUS and S800 biomedical corpora. Our proposed approach surpasses existing methods in linking entities to the NCBI taxonomy. To the best of our knowledge, there is no existing neural network-based approach for species normalization in the literature

Using distributional similarity to organise biomedical terminology

We investigate an application of distributional similarity techniques to the problem of structural organisation of biomedical terminology. Our application domain is the relatively small GENIA corpus. Using terms that have been accurately marked-up by hand within the corpus, we consider the problem of automatically determining semantic proximity. Terminological units are dened for our purposes as normalised classes of individual terms. Syntactic analysis of the corpus data is carried out using the Pro3Gres parser and provides the data required to calculate distributional similarity using a variety of dierent measures. Evaluation is performed against a hand-crafted gold standard for this domain in the form of the GENIA ontology. We show that distributional similarity can be used to predict semantic type with a good degree of accuracy