Fine-Grained Selective Similarity Integration for Drug-Target Interaction Prediction
Bin Liu, Jin Wang, Kaiwei Sun, Grigorios Tsoumakas

TL;DR
This paper introduces FGS, a novel fine-grained similarity integration method for drug-target interaction prediction that improves accuracy by selectively leveraging similarity views at a local level, outperforming existing methods.
Contribution
The study presents a local interaction consistency-based weighting approach for similarity integration, enhancing DTI prediction accuracy over global methods and collaborating effectively with base models.
Findings
FGS outperforms existing similarity integration methods.
FGS achieves better prediction accuracy than state-of-the-art approaches.
Case studies confirm the practical utility of FGS in identifying novel DTIs.
Abstract
The discovery of drug-target interactions (DTIs) is a pivotal process in pharmaceutical development. Computational approaches are a promising and efficient alternative to tedious and costly wet-lab experiments for predicting novel DTIs from numerous candidates. Recently, with the availability of abundant heterogeneous biological information from diverse data sources, computational methods have been able to leverage multiple drug and target similarities to boost the performance of DTI prediction. Similarity integration is an effective and flexible strategy to extract crucial information across complementary similarity views, providing a compressed input for any similarity-based DTI prediction model. However, existing similarity integration methods filter and fuse similarities from a global perspective, neglecting the utility of similarity views for each drug and target. In this study, we…
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Taxonomy
TopicsComputational Drug Discovery Methods · Cholinesterase and Neurodegenerative Diseases · Bioinformatics and Genomic Networks
MethodsBalanced Selection
