4.7 Article

Extraction of microRNA-target interaction sentences from biomedical literature by deep learning approach

Journal

BRIEFINGS IN BIOINFORMATICS
Volume 24, Issue 1, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bibibbac497

Keywords

microRNA (miRNA)-target interaction; deep learning; semantic encoding; language models

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This study constructed a deep learning-based model to efficiently extract miRNA-target interaction knowledge from large-scale published biomedical literature. The model performed outstandingly and outperformed other machine learning methods. This research is of great significance for advancing miRNA analysis and regulation studies.
MicroRNA (miRNA)-target interaction (MTI) plays a substantial role in various cell activities, molecular regulations and physiological processes. Published biomedical literature is the carrier of high -confidence MTI knowledge. However, digging out this knowledge in an efficient manner from large-scale published articles remains challenging. To address this issue, we were motivated to construct a deep learning -based model. We applied the pre -trained language models to biomedical text to obtain the representation, and subsequently fed them into a deep neural network with gate mechanism layers and a fully connected layer for the extraction of MTI information sentences. Performances of the proposed models were evaluated using two datasets constructed on the basis of text data obtained from miRTarBase. The validation and test results revealed that incorporating both PubMedBERT and SciBERT for sentence level encoding with the long short-term memory (LSTM)-based deep neural network can yield an outstanding performance, with both F1 and accuracy being higher than 80% on validation data and test data. Additionally, the proposed deep learning method outperformed the following machine learning methods: random forest, support vector machine, logistic regression and bidirectional LSTM. This work would greatly facilitate studies on MTI analysis and regulations. It is anticipated that this work can assist in large-scale screening of miRNAs, thereby revealing their functional roles in various diseases, which is important for the development of highly specific drugs with fewer side effects. Source code and corpus are publicly available at https://github.com/qi29.

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