ArticleBioinformatics and biology insights2026
Zoon0PredV: Potential Virus Species Crossover Prediction Using Convolutional Neural Networks and Viral Protein Sequence Patterns.
Article in Bioinformatics and biology insights, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
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Who cites it
1 citing paper in PubMed.
- Identifying host-specific patterns in viral protein sequences to predict host spillover risk in animal and plant kingdoms.Scientific reports · 2026Article
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Biomedical science has made substantial progress toward diagnosing, understanding the pathogenesis, and treating various causative agents of infectious disease. However, novel microbial pathogens continue to emerge, and existing pathogens continue to evolve alternative strategies to thrive in ever-changing environments. Various infectious disease etiological agents originate from animal reservoirs, and several have, over time, acquired the ability to cross the species barrier, altering their host range. Computational approaches in biomedical science capable of analyzing large datasets are invaluable for predicting and monitoring disease outbreaks and their effectiveness is greatly enhanced when integrated with machine learning techniques. The goal of this study is to develop a machine learning model for the prediction of potentially zoonotic organisms, using viral surface proteins that facilitate host cell entry as input data. Sequence data and metadata were obtained from UniProtKB, transformed into a machine-readable format, using frequency chaos game representation and a convolutional neural network model was developed to identify sequence patterns consistent with viruses which infect humans. The model achieves generalized performance of 96.78% accuracy, 0.97 F1 score, and 0.93 MCC (Matthews Correlation Coefficient) on unseen data. The model potentially provides a robust framework for application in early identification of emerging viral threats, supporting public health surveillance and risk mitigation.
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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.