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Morphology-guided deep learning for nanoparticle agglomeration diagnostic assays
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  • Published: 31 March 2026

Morphology-guided deep learning for nanoparticle agglomeration diagnostic assays

  • Kartik Jhawar1,2 na1,
  • Xiao-Liu Chu1 na1,
  • Joseph B. DeGrandchamp1 na1,
  • Yueming Yin1,3,
  • Lalitha Anjali Peddibhotla1,4,
  • Shabina Banu1,4,
  • Farah Najwa Nabila Mohd Hatta1,5,
  • Yaoli Wang6,
  • Peter Török1,7,8,9 &
  • …
  • Lipo Wang1,2 

Scientific Reports , Article number:  (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biological techniques
  • Biotechnology
  • Computational biology and bioinformatics
  • Nanoscience and technology

Abstract

Accurate and rapid diagnostic tests that are simultaneously affordable remain elusive, typically due to trade-offs between performance and cost. Conventional nucleic acid tests offer high sensitivity but require complex, expensive steps such as amplification and purification, whereas lateral flow assays are simple and low-cost but lack the necessary sensitivity for many applications. New analytical approaches provide an opportunity to bridge this gap, raising sensitivity but not material expense. We present a miniaturized and simplified chip-based platform that combines three components into a single diagnostic pipeline: we use (i) spectrally distinct silver and gold nanoparticles (NPs) that form analyte-dependent clusters with unique spectral fingerprints, (ii) a one-pot, enzyme- and purification-free assay on a chip integrated with a high-throughput automated low-cost microscope, and (iii) a morphology-guided convolutional Graph Neural Network that embeds morphology information into convolutional kernels and performs graph-based relational learning across particle-level features. This integration captures spectral, spatial, and morphological quantification at the particle level, rather than relying on bulk spectral shifts, thereby addressing key limitations observed in representative nanoparticle (NP) assays and image-level deep learning baselines under particle-parallel analysis. Mc-GNN is able to process up to 5,000 particle crops per image in a single computational step, using less than 2 GB of GPU memory. This allows us to achieve femtomolar sensitivity with 98.2% recall for synthetic DNA and 94.8% for SARS-CoV-2 RNA from whole viruses, within in-domain experimental variability arising from different NP combinations and assay conditions. By embedding morphological information into the biosensing pipeline, our diagnostic platform is computationally efficient with millisecond-scale neural compute per raw image on a single consumer-grade GPU and is readily extensible to new analytes and multiplexing, offering a scalable solution for a fieldable diagnostic tool.

Data availability

Representative example data and processed outputs used for demonstration and reproducibility are publicly available at https://github.com/kartik05112000/Mc_GNN_Analysis.git. The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.

Code availability

The full source code for Mc-GNN, together with scripts for preprocessing, training, evaluation, and representative example data, is publicly available at https://github.com/kartik05112000/Mc_GNN_Analysis.git. Additional datasets and experimental data supporting the findings of this study are available from the corresponding author on reasonable request.

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Acknowledgements

We thank Professor Atul N. Parikh (NTU - Singapore and UC Davis) for valuable discussions and for reviewing the final manuscript. This research is supported by the Ministry of Education, Singapore, under its Research Centre of Excellence award to the Institute for Digital Molecular Analytics and Science, NTU (IDMxS, grant: EDUNC-33-18-279-V12). Figure 2a contains art adapted from Servier Medical Art (https://smart.servier.com/), licensed under CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/).

Funding

This research is supported by the Ministry of Education, Singapore, under its Research Centre of Excellence award to the Institute for Digital Molecular Analytics and Science, NTU (IDMxS, grant: EDUNC-33-18-279-V12).

Author information

Author notes
  1. Kartik Jhawar, Xiao-Liu Chu and Joseph B. DeGrandchamp contributed equally to this work.

Authors and Affiliations

  1. Institute for Digital Molecular Analytics and Science, Nanyang Technological University, Singapore, 636921, Singapore

    Kartik Jhawar, Xiao-Liu Chu, Joseph B. DeGrandchamp, Yueming Yin, Lalitha Anjali Peddibhotla, Shabina Banu, Farah Najwa Nabila Mohd Hatta, Peter Török & Lipo Wang

  2. School of Electrical and Electronic Engineering, Nanyang Technological University, Singapore, 639798, Singapore

    Kartik Jhawar & Lipo Wang

  3. College of Computing and Data Science, Nanyang Technological University, Singapore, 639798, Singapore

    Yueming Yin

  4. Republic Polytechnic, Singapore, 738964, Singapore

    Lalitha Anjali Peddibhotla & Shabina Banu

  5. Universiti Putra Malaysia, 43400, Serdang, Malaysia

    Farah Najwa Nabila Mohd Hatta

  6. College of Electronic and Information Engineering, Taiyuan University of Technology, Taiyuan, China

    Yaoli Wang

  7. Singapore Centre for Environmental Life Sciences Engineering, Nanyang Technological University, Singapore, 637551, Singapore

    Peter Török

  8. Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore, 636921, Singapore

    Peter Török

  9. School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore, 637371, Singapore

    Peter Török

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  1. Kartik Jhawar
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Contributions

K.J., X-L.C., and J.B.D. contributed equally to this work. K.J., X-L.C., J.B.D., P.T. and L.W. performed conceptualization. X-L.C., J.B.D., L.A.P., S.B., and F.N.N.M.H. performed experimental investigation. K.J. developed the data processing and deep learning method, carried out model training, and analyzed the results. Y.Y. and Y.W. contributed to model-related discussions. P.T. and L.W. performed supervision. K.J., X-L.C., and J.B.D. wrote the original manuscript draft. All authors contributed to review and editing of the final manuscript.

Corresponding authors

Correspondence to Peter Török or Lipo Wang.

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Jhawar, K., Chu, XL., DeGrandchamp, J.B. et al. Morphology-guided deep learning for nanoparticle agglomeration diagnostic assays. Sci Rep (2026). https://doi.org/10.1038/s41598-026-45423-2

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  • Received: 07 November 2025

  • Accepted: 18 March 2026

  • Published: 31 March 2026

  • DOI: https://doi.org/10.1038/s41598-026-45423-2

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Keywords

  • Morphology-guided convolution
  • Graph neural network
  • Optical barcodes
  • Dark-field microscopy
  • NP clustering
  • SARS-CoV-2
  • Femtomolar sensitivity
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