Yile Sun

ORCID: 0000-0003-2889-6155
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Research Areas
  • Advanced Fluorescence Microscopy Techniques
  • Optical Coherence Tomography Applications
  • Photoacoustic and Ultrasonic Imaging
  • Cell Image Analysis Techniques
  • Advanced Electron Microscopy Techniques and Applications
  • Image Processing Techniques and Applications
  • Multimodal Machine Learning Applications
  • Natural Language Processing Techniques
  • Digital Holography and Microscopy
  • Advanced X-ray and CT Imaging
  • Integrated Circuits and Semiconductor Failure Analysis
  • Topic Modeling
  • Force Microscopy Techniques and Applications
  • Advanced Radiotherapy Techniques
  • Near-Field Optical Microscopy
  • Advanced X-ray Imaging Techniques
  • Photonic and Optical Devices
  • Video Analysis and Summarization
  • Medical Imaging Techniques and Applications
  • CCD and CMOS Imaging Sensors

University of Michigan
2025

Zhejiang University
2021-2024

State Key Laboratory of Modern Optical Instruments
2022-2023

Observing subcellular structural dynamics in living cells has become the goal of super-resolution (SR) fluorescence microscopy. Among typical SRM techniques, structured illumination microscopy (SIM) stands out for its fast imaging speed and low photobleaching. However, 2D-SIM requires nine raw images to obtain a SR image, leading undesirable artifacts live-cell imaging. In this paper, we propose single-frame (SF-SIM) method based on deep learning that achieves using only single image...

10.1063/5.0180978 article EN cc-by APL Photonics 2024-03-01

Modulation-enhanced localization microscopy (MELM) has demonstrated significant improvements in both lateral and axial precision compared to conventional single-molecule (SMLM). However, modulated illumination based MELM (MELMxy) remains fundamentally limited two-dimensional imaging. Here we present three-dimensional Single-Molecule Modulated Illumination Localization Estimator (SMILE) that synergistically integrates modulation with point spread function engineering. By simultaneously...

10.48550/arxiv.2502.14243 preprint EN arXiv (Cornell University) 2025-02-19

Imaging three-dimensional, subcellular structures with high axial resolution has always been the core purpose of fluorescence microscopy. However, trade-offs exist between and other important technical indicators, such as temporal resolution, optical power density, imaging process complexity. We report a new modality, interference structured illumination microscopy (FI-SIM), which is based on three-dimensional for wide-field lateral reconstruction. FI-SIM can acquire images quickly within...

10.1117/1.ap.5.5.056007 article EN cc-by Advanced Photonics 2023-09-19

Structured-illumination microscopy (SIM) offers a twofold resolution enhancement beyond the optical diffraction limit. At present, SIM requires several raw structured-illumination (SI) frames to reconstruct super-resolution (SR) image, especially time-consuming reconstruction of speckle SIM, which hundreds SI frames. Considering this, we herein propose an untrained neural network (USRNN) with known illumination patterns reduce amount data that is required for by 20 times and thus improve its...

10.1364/ol.511983 article EN Optics Letters 2024-03-14

Three-dimensional structured illumination microscopy (3D-SIM) plays an essential role in biological volumetric imaging with the capabilities of improving lateral and axial resolution. However, traditional linear 3D algorithm is sensitive to noise generates artifacts, while low temporal resolution hinders live-cell imaging. In this paper, we propose a novel 3D-SIM based on total variation (TV) fast iterative shrinkage threshold (FISTA), termed TV-FISTA-SIM. Compared conventional algorithms,...

10.1364/oe.451190 article EN cc-by Optics Express 2022-02-14

Optical microscopy is an essential tool for exploring the structures and activities of cells tissues. To break limit resolution caused by diffraction, researchers have made continuous advances innovations to improve optical since 1990s. These contributions, however, still make sub-10[Formula: see text]nm imaging obstacle. Here, we name a series technologies as modulated illumination localization (MILM), which makes ultra-high-resolution practical. Besides, review recent progress 2017 when...

10.1142/s179354582230004x article EN cc-by Journal of Innovative Optical Health Sciences 2022-02-16

Single-molecule localization microscopy (SMLM) gradually plays an important role in deep tissue imaging. However, current SMLM methods primarily rely on fiducial marks, neglecting aberrations introduced by thick samples, thereby resulting decreased image quality tissues. Here, we introduce vectorial situ point spread function (PSF) retrieval (VISPR), a method that retrieves precise PSF model considering both system- and sample-induced under conditions. By employing the theory of maximum...

10.1364/prj.520469 article EN Photonics Research 2024-08-12

Three-dimensional structured illumination microscopy (3D-SIM) is an essential tool for volumetric fluorescence imaging, which improves both axial and lateral resolution by down-modulating high-frequency information of the sample into passband optical transfer function (OTF). And when combining with 4Pi structure, performance 3D-SIM can be further improved. The reconstruction results generally used linear 3D algorithm, however, are lack high-fidelity proneess to generate artifacts. In this...

10.1364/oe.424740 article EN cc-by Optics Express 2021-06-11

Structured illumination microscopy (SIM) achieves super-resolution (SR) by modulating the high-frequency information of sample into passband optical system and subsequent image reconstruction. The traditional Wiener-filtering-based reconstruction algorithm operates in Fourier domain, it requires prior knowledge sinusoidal patterns which makes time-consuming procedure parameter estimation to raw datasets necessary, besides, is sensitive noise or aberration-induced pattern distortion leads...

10.1142/s1793545823500219 article EN cc-by Journal of Innovative Optical Health Sciences 2023-07-21

As a supplement to optical super-resolution microscopy techniques, computational methods have demonstrated remarkable results in alleviating the spatiotemporal imaging trade-off. However, they commonly suffer from low structural fidelity and universality. Therefore, we herein propose deep-physics-informed sparsity framework designed holistically synergize strengths of physical models (image blurring processes), prior knowledge (continuity constraints), back-end optimization algorithm...

10.34133/icomputing.0082 article EN cc-by Intelligent Computing 2024-01-01

This paper introduces a novel probabilistic mapping algorithm, Latent BKI, which enables open-vocabulary with quantifiable uncertainty. Traditionally, semantic algorithms focus on fixed set of categories limits their applicability for complex robotic tasks. Vision-Language (VL) models have recently emerged as technique to jointly model language and visual features in latent space, enabling recognition beyond predefined, classes. BKI recurrently incorporates neural embeddings from VL into...

10.48550/arxiv.2410.11783 preprint EN arXiv (Cornell University) 2024-10-15

Abstract Spatial resolution is crucial for imaging subcellular structures. The advent of three-dimensional structured illumination microscopy (3D-SIM) greatly benefits the biology community providing a powerful tool organelles with two-fold enhancement in all three dimensions. However, axial 3D-SIM limited to around 300 nm, which inferior its lateral resolution. Here we report novel method, image interference SIM(I 2 SIM), utilizes two oppositely positioned objectives detect fluorescence...

10.1101/2024.12.18.629092 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2024-12-21

The dipole orientation of fluorescent molecules reveals the structural organization at subcellular level, and imaging its distribution is important for fundamental cell biology studies. Using conventional fluorescence microscopy, dipoles can be obtained by demodulating polarization states through excitation or emission processes. recent introduction structured illumination microscopy (SIM) has improved axial lateral resolution to around 300 100 nm, respectively. However, still very limited,...

10.1021/acsphotonics.4c01807 article EN ACS Photonics 2024-12-29

In recent years, modulated illumination localization microscopy (MILM) methods have been proposed to provide around two-fold improvement in lateral precision over conventional single molecule with the same photon budget. However, MILM laterally was so far reported two-dimensional imaging modalities. To fully exploit its three-dimensional (3D) potential, we propose a 3D Single-Molecule Modulated Illumination Localization Estimator (3D-SMILE) that uses raw data measured from MILM, which has...

10.1117/12.2648821 article EN 2023-03-15

Abstract In single-molecule localization microscopy (SMLM), achieving precise hinges on obtaining an authentic point spread function (PSF) influenced by system and sample-induced aberrations. Here, we introduce VISPR (Vectorial in-situ PSF retrieval) retrieving 3D models considering both aberrations under SMLM conditions. By employing the theory of vectorial model maximum likelihood estimation (MLE) phase retrieval, is capable reconstructing accurate theoretically minimum uncertainty...

10.1101/2023.11.03.565592 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2023-11-05
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