Publications by authors named "Ivy H M Wong"

Article Synopsis
  • Slide-free imaging techniques are improving the histological workflow, with CHAMP offering high resolution but relying on an expensive ultraviolet laser.
  • The proposed EW-LED framework uses a low-cost LED and deep learning to achieve results comparable to CHAMP, significantly reducing costs and time.
  • EW-LED cuts costs by 85× and shortens image acquisition and computation times by 36× and 17×, respectively, and can be applied to enhance other imaging methods for better virtual histology.
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Deep learning algorithms have been widely used in microscopic image translation. The corresponding data-driven models can be trained by supervised or unsupervised learning depending on the availability of paired data. However, general cases are where the data are only roughly paired such that supervised learning could be invalid due to data unalignment, and unsupervised learning would be less ideal as the roughly paired information is not utilized.

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Lung adenocarcinoma (LUAD) is the most common primary lung cancer and accounts for 40% of all lung cancer cases. The current gold standard for lung cancer analysis is based on the pathologists' interpretation of hematoxylin and eosin (H&E)-stained tissue slices viewed under a brightfield microscope or a digital slide scanner. Computational pathology using deep learning has been proposed to detect lung cancer on histology images.

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Rapid multicolor three-dimensional (3D) imaging for centimeter-scale specimens with subcellular resolution remains a challenging but captivating scientific pursuit. Here, we present a fast, cost-effective, and robust multicolor whole-organ 3D imaging method assisted with ultraviolet (UV) surface excitation and vibratomy-assisted sectioning, termed translational rapid ultraviolet-excited sectioning tomography (TRUST). With an inexpensive UV light-emitting diode (UV-LED) and a color camera, TRUST achieves widefield exogenous molecular-specific fluorescence and endogenous content-rich autofluorescence imaging simultaneously while preserving low system complexity and system cost.

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Ultraviolet photoacoustic microscopy (UV-PAM) has been investigated to provide label-free and registration-free volumetric histological images for whole organs, offering new insights into complex biological organs. However, because of the high UV absorption of lipids and pigments in tissue, UV-PAM suffers from low image contrast and shallow image depth, hindering its capability for revealing various microstructures in organs. To improve the UV-PAM imaging contrast and imaging depth, here we propose to implement a state-of-the-art optical clearing technique, CUBIC (clear, unobstructed brain/body imaging cocktails and computational analysis), to wash out the lipids and pigments from tissues.

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Article Synopsis
  • - The authors introduce a new histological imaging technique called CHAMP (computational high-throughput autofluorescence microscopy by pattern illumination) that allows for quick, label-free imaging of thick tissue samples at a speed of 10 mm every 10 seconds and with a lateral resolution of 1.1 µm.
  • - CHAMP can rapidly convert raw images into virtually stained histological images (Deep-CHAMP) using advanced computing methods, enabling the extraction of important cellular features in just 15 seconds.
  • - The method has been successfully tested on various tissues, including mouse brain, kidney, and human lung, showing its potential for facilitating fast and accurate pathological examinations during surgeries without the need for traditional tissue processing or staining
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Histopathological examination of tissue sections is the gold standard for disease diagnosis. However, the conventional histopathology workflow requires lengthy and laborious sample preparation to obtain thin tissue slices, causing about a one-week delay to generate an accurate diagnostic report. Recently, microscopy with ultraviolet surface excitation (MUSE), a rapid and slide-free imaging technique, has been developed to image fresh and thick tissues with specific molecular contrast.

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