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Insensitive Nuclei Enhanced by Polarization Transfer (INEPT) is an advanced Nuclear Magnetic Resonance (NMR) technique specifically designed to detect and enhance the signals of low-abundance nuclei, such as carbon-13 and nitrogen-15, in small molecules. The fundamental principle behind INEPT is the transfer of polarization from a more abundant and highly polarizable nucleus, typically hydrogen-1, to the low-abundance nucleus of interest. This process effectively boosts the NMR signal of the...

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Correction: Komatsu et al. Three-Dimensional Visualization and Detection of the Pulmonary Venous-Left Atrium Connection Using Artificial Intelligence in Fetal Cardiac Ultrasound Screening. <i>Bioengineering</i> 2026, <i>13</i>, 100.

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From Pixels to Precision-A Dual-Stream Deep Network for Pathological Nuclei Segmentation.

Rashid Nasimov1, Kudratjon Zohirov2, Adilbek Dauletov3

  • 1Department of Computer Engineering, Gachon University Sujeong-Gu, Seongnam-si 13120, Gyeonggi-Do, Republic of Korea.

Bioengineering (Basel, Switzerland)
|August 28, 2025
PubMed
Summary
This summary is machine-generated.

A new deep learning model, Dual-Stream HyperFusionNet (DS-HFN), accurately segments cell nuclei in histopathology images. This computational pathology tool balances context and precision for improved disease diagnosis and biomarker analysis.

Keywords:
biomedical image processingdeep learning in pathologydual-stream networkhistopathological image analysisnuclei segmentation

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Area of Science:

  • Computational pathology
  • Digital pathology
  • Biomedical image analysis

Background:

  • Accurate cell nuclei segmentation is crucial for computational pathology, impacting disease diagnosis and biomarker analysis.
  • Existing deep learning models struggle to balance global context with precise boundary detection, especially for overlapping or deformed nuclei.

Purpose of the Study:

  • To introduce a novel deep learning model, Dual-Stream HyperFusionNet (DS-HFN), for robust and accurate cell nuclei segmentation.
  • To address the challenge of integrating semantic context and fine boundary details in histopathological images.

Main Methods:

  • DS-HFN employs a dual-stream encoder to capture semantic and edge-focused features simultaneously.
  • An attention-driven HyperFeature Embedding Module (HFEM) fuses these features.
  • A dual-decoder architecture and Gradient-Aligned Loss Function enhance structural precision.

Main Results:

  • DS-HFN outperformed 30 state-of-the-art models across benchmark datasets (TNBC, MoNuSeg) in all evaluation metrics.
  • The model demonstrated superior accuracy in nuclei segmentation compared to existing methods.
  • DS-HFN also showed reduced computational expense.

Conclusions:

  • DS-HFN offers a robust solution for accurate cell nuclei segmentation in digital pathology.
  • The model's ability to precisely delineate nuclei is vital for clinical diagnosis and biomarker analysis.
  • DS-HFN advances the field of computational pathology by improving segmentation accuracy and efficiency.