ArticleACS omega2025
Multimodal Deep Learning for Generating Potential Anti-Dengue Peptides.
Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- Molecular active learning approaches for predicting skin cytotoxicity.Molecular diversity · 2026Article
- Exploring anti-dengue activity with atomic-weighted vectors, class balancing and machine learning.Molecular diversity · 2026Article
- Accurate structure-activity relationship prediction of antioxidant peptides using a multimodal deep learning framework.Journal of cheminformatics · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Dengue virus remains a significant global health threat, imposing a substantial disease burden on nearly half of the world's population. The urgent need for effective antiviral therapeutics, including therapeutic peptides targeting the Dengue virus, is critical in the current healthcare landscape. However, the availability of anti-Dengue peptides (ADPs) data remains limited in existing data sets, posing a challenge for computational modeling and discovery. This study presents a novel multimodal framework integrating high-performance predictive modeling with generative learning to accurately predict and potentially identify novel potent ADPs. Specifically, a predictive model was constructed using a multimodal combination of bidirectional long short-term memory (BiLSTM) and a stacking ensemble of neural networks, both using diverse sequence representations. Additionally, a Wasserstein generative adversarial network with a gradient penalty was employed to generate novel ADP candidates. The predictive models demonstrated robust performance, achieving balanced accuracy, area under the receiver operating characteristic curve, and area under the precision-recall curve exceeding 90%, with a Matthews correlation coefficient surpassing 80%. In addition, glycine (G), phenylalanine (F), and tryptophan (W) are the most influential residues to the inhibitory potency of ADPs. Through the proposed multimodal framework, 33 novel ADP sequences with the highest predictive probabilities were identified. Furthermore, regression analysis using a random forest model was developed to predict three candidate peptides with predicted IC
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.