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Preparation of Whole Bone Marrow for Mass Cytometry Analysis of Neutrophil-lineage Cells
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NoTAC: A Noise-Tolerance Automatic Cleaning Framework for Bone Marrow Karyotyping Data.

Rihan Huang, Siyuan Chen, Yafei Li

    IEEE Journal of Biomedical and Health Informatics
    |August 1, 2025
    PubMed
    Summary
    This summary is machine-generated.

    We developed NoTAC, a novel framework to automatically clean noisy chromosome data for deep neural network (DNN) training. This improves chromosome classification accuracy in medical diagnostics.

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    Area of Science:

    • Bioinformatics
    • Computational Biology
    • Medical Imaging

    Background:

    • Deep neural networks (DNNs) are crucial for chromosome classification in karyotyping and disease diagnosis.
    • Clinical chromosome datasets often suffer from label errors and outliers, hindering DNN performance and clinical use.

    Purpose of the Study:

    • To introduce NoTAC, a Noise-Tolerance Automatic Cleaning framework, designed to enhance DNN-based chromosome classification.
    • To address and mitigate the impact of labeling errors and outliers in medical image datasets.

    Main Methods:

    • NoTAC employs a two-branch approach: KaryoCleanse for label noise detection and KaryoDrift for outlier identification.
    • Label noise is detected using DNN self-confidence, latent label distribution estimation, and probability ranking.
    • Outliers are identified and removed by scoring samples based on average K-nearest neighbor distances.

    Main Results:

    • NoTAC achieved a 93.99% accuracy on an R-band bone marrow chromosome dataset, a 6.25% relative improvement over baselines.
    • The framework outperformed state-of-the-art noise-handling methods by 0.92%.
    • Qualitative analysis revealed data issues impacting DNN predictions, offering insights into data quality's role.

    Conclusions:

    • NoTAC effectively enhances the performance and reliability of DNNs for practical medical datasets.
    • The framework demonstrates potential for improving clinical karyotype diagnosis by ensuring data quality.