A Multimodal Neural Fusion Framework by Integrating T-CNN and L-DL for Drug Discovery

With the pace of artificial intelligence and big data analytics, artificial intelligence is easily revolutionizing the drug discovery process. Conventional approaches usually rely on static representations of data that fail to capture complex dynamics within biological systems or temporal evolution of interactions between drugs. In this paper a novel multimodal neural fusion framework for adding a temporal dimension into the realm of drug discovery is proposed. With heterogeneous types of data: chemical, biological, genomic, and clinical data, the framework can learn to understand drug interactions and patient-specific responses. Innovations include dynamic Graph Neural Network for time-evolving molecular interactions modeling, Temporal Convolutional Neural Networks(T-CNN) to capture time-dependent features, and the L-DL component focuses on chronic disease outcomes. Label Distribution Learning (LDL) is a machine learning paradigm where each instance is associated with a label distribution representing the degree of relevance of multiple labels. The proposed architecture supports drug effects to be analyzed real-time, enables treatment to be devised on a per-patient basis, and allows clinical trials to adapt their strategy based on evolving treatment effects. We showcase this framework with extensive experiments by achieving higher predictive accuracy compared to other state-of-the-art approaches and demonstrating how it could be the paradigm shift in drug discovery science. This approach does not only overcome the limitation of existing methodologies but also opens up avenues for personalized medicine in clinical settings. The proposed method achieved an accuracy of 94.7%, with precision, recall, and F1-score improvements of 92.3%, 93.5%, and 92.9%, respectively, surpassing existing approaches in drug discovery.

Authors

Institutions

Publication Details

Published
2025-04-23
DOI
https://doi.org/10.1109/raeeucci63961.2025.11048328
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A Multimodal Neural Fusion Framework by Integrating T-CNN and L-DL for Drug Discovery

S. M., S.V. Divya, J. Balaji, P. Venkadesh et al.
Computational Drug Discovery Methods
article

A Multimodal Neural Fusion Framework by Integrating T-CNN and L-DL for Drug Discovery

S. M., S.V. Divya, J. Balaji, P. Venkadesh, S. Yazhini, B. Selvapriya
article en

Abstract

With the pace of artificial intelligence and big data analytics, artificial intelligence is easily revolutionizing the drug discovery process. Conventional approaches usually rely on static representations of data that fail to capture complex dynamics within biological systems or temporal evolution of interactions between drugs. In this paper a novel multimodal neural fusion framework for adding a temporal dimension into the realm of drug discovery is proposed. With heterogeneous types of data: chemical, biological, genomic, and clinical data, the framework can learn to understand drug interactions and patient-specific responses. Innovations include dynamic Graph Neural Network for time-evolving molecular interactions modeling, Temporal Convolutional Neural Networks(T-CNN) to capture time-dependent features, and the L-DL component focuses on chronic disease outcomes. Label Distribution Learning (LDL) is a machine learning paradigm where each instance is associated with a label distribution representing the degree of relevance of multiple labels. The proposed architecture supports drug effects to be analyzed real-time, enables treatment to be devised on a per-patient basis, and allows clinical trials to adapt their strategy based on evolving treatment effects. We showcase this framework with extensive experiments by achieving higher predictive accuracy compared to other state-of-the-art approaches and demonstrating how it could be the paradigm shift in drug discovery science. This approach does not only overcome the limitation of existing methodologies but also opens up avenues for personalized medicine in clinical settings. The proposed method achieved an accuracy of 94.7%, with precision, recall, and F1-score improvements of 92.3%, 93.5%, and 92.9%, respectively, surpassing existing approaches in drug discovery.

Sathyabama Institute of Science and Technology (IN)
Openalex Percentile: Top 83%
Computational Drug Discovery Methods
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.