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RNA viruses are categorized into positive-strand, negative-strand, or double-stranded groups based on their genomic structure and replication mechanisms. This classification dictates how they exploit host cellular machinery for protein synthesis and replication. Some RNA viruses also utilize reverse transcription as part of their life cycle, further diversifying their replication strategies.Positive-Strand RNA VirusesPositive-strand RNA viruses have genomes that function directly as messenger...
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DNA Virus Detection System Based on RPA-CRISPR/Cas12a-SPM and Deep Learning
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Interpretability-driven deep learning for SERS-based classification of respiratory viruses.

Hyunju Kang1, Junhyeong Lee2, Soo Hyun Lee3

  • 1Department of Chemistry, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Republic of Korea; Bionanotechnology Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, 34141, Republic of Korea.

Biosensors & Bioelectronics
|August 21, 2025
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Summary
This summary is machine-generated.

A new diagnostic platform uses 3D plasmonic nanopillars and deep learning to rapidly detect multiple respiratory viruses, including SARS-CoV-2 variants, with over 98% accuracy. This technology offers a scalable, label-free solution for accurate, real-world diagnostics.

Keywords:
CNNGrad-CAMPlasmonic nanostructureRespiratory virusSERS

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Area of Science:

  • Nanotechnology
  • Biomedical Engineering
  • Machine Learning

Background:

  • Respiratory viruses like influenza, RSV, and SARS-CoV-2 pose significant global health risks.
  • Accurate and rapid variant-level diagnostics are crucial for managing outbreaks.
  • Existing diagnostic methods may lack speed, accuracy, or the ability to differentiate specific variants.

Purpose of the Study:

  • To develop an integrated diagnostic platform for the rapid detection and differentiation of multiple respiratory viruses.
  • To leverage surface-enhanced Raman scattering (SERS) and 3D plasmonic nanopillars for enhanced viral detection.
  • To apply interpretability-driven deep learning for accurate virus classification and model transparency.

Main Methods:

  • Development of a diagnostic platform utilizing 3D plasmonic nanopillar substrates for enhanced SERS signal acquisition.
  • Training a one-dimensional convolutional neural network (1D-CNN) on SERS spectra from 13 respiratory virus types, including SARS-CoV-2 variants.
  • Application of gradient-weighted class activation mapping (Grad-CAM) to identify critical Raman shift regions for virus discrimination.

Main Results:

  • Achieved over 98% classification accuracy in identifying 13 respiratory virus types using the 1D-CNN model.
  • Demonstrated robust and reproducible capture of viral components, enhancing SERS signals for molecular fingerprinting.
  • Validated reliable performance in complex clinical samples, confirming real-world applicability.

Conclusions:

  • The developed platform provides a scalable, label-free solution for rapid, accurate, and variant-level respiratory virus detection.
  • The integration of 3D SERS substrates and deep learning enhances diagnostic capabilities.
  • The technology holds potential for point-of-care applications and improved epidemiological surveillance.