Minho Eom

ORCID: 0000-0003-4068-5246
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About
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Research Areas
  • Advanced Fluorescence Microscopy Techniques
  • Integrated Circuits and Semiconductor Failure Analysis
  • Advanced Electrical Measurement Techniques
  • Electrical and Bioimpedance Tomography
  • Cell Image Analysis Techniques
  • Advanced Electron Microscopy Techniques and Applications
  • Zebrafish Biomedical Research Applications
  • Force Microscopy Techniques and Applications
  • Image and Signal Denoising Methods
  • Photoacoustic and Ultrasonic Imaging
  • Neuroscience and Neural Engineering
  • Cell Adhesion Molecules Research
  • Digital Holography and Microscopy
  • Photoreceptor and optogenetics research
  • Optical Imaging and Spectroscopy Techniques
  • Neuroscience and Neuropharmacology Research
  • Neural dynamics and brain function

Korea Advanced Institute of Science and Technology
2021-2025

Abstract Here we report SUPPORT (statistically unbiased prediction utilizing spatiotemporal information in imaging data), a self-supervised learning method for removing Poisson–Gaussian noise voltage data. is based on the insight that pixel value data highly dependent its neighboring pixels, even when temporally adjacent frames alone do not provide useful statistical prediction. Such dependency captured and used by convolutional neural network with blind spot to accurately denoise which...

10.1038/s41592-023-02005-8 article EN cc-by Nature Methods 2023-09-18

Nanoscale imaging of whole vertebrates is essential for the systematic understanding human diseases, yet this goal has not been achieved. Expansion microscopy (ExM) an attractive option accomplishing aim; however, expansion even mouse embryos at mid- and late-developmental stages, which have fewer calcified body parts than adult mice, to be demonstrated due challenges expanding tissues. Here, we introduce a state-of-the-art ExM technique, termed whole-body ExM, that utilizes cyclic...

10.1021/acsnano.4c14791 article EN ACS Nano 2025-02-18

ABSTRACT Nanoscale resolution imaging of whole vertebrates is required for a systematic understanding human diseases, but this has yet to be realized. Expansion microscopy (ExM) an attractive option achieving goal, the expansion not been demonstrated due difficulty expanding hard body components. Here, we demonstrate whole-body ExM, which enables nanoscale anatomical structures, proteins, and endogenous fluorescent proteins (FPs) zebrafish larvae mouse embryos by them fourfold. We first show...

10.1101/2021.05.18.443629 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2021-05-18

Abstract Recent advancements in genetically encoded calcium indicators, particularly those based on green fluorescent proteins, have optimized their performance for monitoring neuronal activities a variety of model organisms. However, progress developing red-shifted GECIs, despite advantages over has been slower, resulting fewer options end-users. In this study, we explored topological inversion and soma-targeting strategies, which are complementary to conventional mutagenesis, re-engineer...

10.1101/2025.01.31.635851 preprint EN cc-by bioRxiv (Cold Spring Harbor Laboratory) 2025-02-02

This review explores how artificial intelligence (AI) is transforming fluorescence microscopy, providing an overview of its fundamental principles and recent advancements. The roles AI in improving image quality introducing new imaging modalities are discussed, offering a comprehensive perspective on these changes. Additionally, unified framework introduced for comprehending AI‐driven microscopy methodologies categorizing them into linear inverse problem‐solving, denoising, nonlinear...

10.1002/adpr.202300308 article EN cc-by Advanced Photonics Research 2024-07-15

Established methods for imaging the living mammalian brain have, to date, taken optical properties of tissue as fixed; we here demonstrate that it is possible modify itself significantly enhance at-depth while preserving native physiology. Using a small amount any several biocompatible materials raise refractive index solutions superfusing prior imaging, could increase several-fold signals from deepest cells normally visible and, under both one-photon and two-photon visualize previously too...

10.1101/2024.09.05.611421 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2024-09-07

As a vertebrate model animal, larval zebrafish are widely used in neuroscience and provide unique opportunity to monitor whole-brain activity at the cellular resolution. Here, we an optimized protocol for performing imaging of using three-dimensional fluorescence microscopy, including sample preparation immobilization, embedding, image acquisition, visualization after imaging. The current enables vivo structure neuronal brain resolution over 1 h confocal microscopy custom-designed...

10.3791/65218 article EN Journal of Visualized Experiments 2023-04-28

As a vertebrate model animal, larval zebrafish are widely used in neuroscience and provide unique opportunity to monitor whole-brain activity at the cellular resolution. Here, we an optimized protocol for performing imaging of using three-dimensional fluorescence microscopy, including sample preparation immobilization, embedding, image acquisition, visualization after imaging. The current enables vivo structure neuronal brain resolution over 1 h confocal microscopy custom-designed...

10.3791/65218-v article EN 2023-04-29

ABSTRACT Here we report SUPPORT (Statistically Unbiased Prediction utilizing sPatiOtempoRal information in imaging daTa), a self-supervised learning method for removing Poisson-Gaussian noise voltage data. is based on the insight that pixel value data highly dependent its spatially neighboring pixels same time frame, even when temporally adjacent frames do not provide useful statistical prediction. Such spatiotemporal dependency captured and utilized to accurately denoise which existence of...

10.1101/2022.11.17.516709 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2022-11-18
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