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    This study introduces a novel unsupervised domain adaptation method for White Blood Cell (WBC) classification, eliminating the need for target data. The approach finds a "closest-clone" from source data to adapt models, improving accuracy in diverse imaging conditions.

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    Area of Science:

    • Medical image analysis
    • Computer vision
    • Machine learning

    Background:

    • Automating White Blood Cell (WBC) classification from microscopic images is crucial for efficient diagnosis.
    • Deep learning models face performance degradation due to domain shift caused by varying imaging conditions.
    • Unsupervised Domain Adaptation (UDA) methods typically require substantial unlabeled target data, which is often unavailable in medical imaging.

    Purpose of the Study:

    • To develop a UDA method for WBC classification that does not require any target data.
    • To address the challenge of domain shift in microscopic image analysis without relying on unlabeled target samples.

    Main Methods:

    • Proposes a novel UDA technique that identifies a 'closest-clone' from source data for a given target test image.
    • Utilizes a latent-variable generative model based on variational inference for simultaneous sampling and closest-clone identification.
    • Employs an optimization procedure in the latent space to find the closest source data proxy.

    Main Results:

    • Demonstrates the efficacy of the proposed method over State-Of-The-Art (SOTA) UDA techniques.
    • Achieves robust WBC classification performance across datasets captured with different imaging modalities and settings.
    • Validates the method's ability to overcome domain shift without target data.

    Conclusions:

    • The proposed data-free UDA method effectively handles domain shift in WBC classification.
    • This approach offers a promising solution for medical image analysis where labeled or unlabeled target data is scarce.
    • The method advances automated diagnostic tools by improving model generalizability across diverse imaging environments.