Evidence map›Paper›PMID 40918327›Full record

ArticleACS omega2025

Multimodal Deep Learning for Generating Potential Anti-Dengue Peptides.

Huynh Anh Duy, Tarapong Srisongkram

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Huynh Anh DuyGraduate School in the Program of Research and Development in Pharmaceuticals, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand.
Tarapong SrisongkramDivision of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand.ORCID https://orcid.org/0000-0001-8512-5379

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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

PMID40918327
PMCPMC12409549

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.