Single-pixel imaging can capture a scene without a direct line of sight to the object but high-quality imaging has proven challenging. Here, by acquiring their Fourier spectrum, Zhang et al. demonstrate indirect, high-quality single-pixel imaging in the presence of noisy environmental illumination.

Single-pixel imaging by means of Fourier spectrum acquisition

Machine vision significantly improves the efficiency, quality, and reliability of defect detection. In visual inspection, excellent optical illumination platforms and suitable image acquisition hardware are the prerequisites for obtaining high-quality images. Image processing and analysis are key technologies in obtaining defect information, while deep learning is significantly impacting the field of image analysis. In this study, a brief history and the state of the art in optical illumination, image acquisition, image processing, and image analysis in the field of visual inspection are systematically discussed. The latest developments in industrial defect detection based on machine vision are introduced. In the further development of the field of visual inspection, the application of deep learning will play an increasingly important role. Thus, a detailed description of the application of deep learning in defect classification, localization and segmentation follows the discussion of traditional defect detection algorithms. Finally, future prospects for the development of visual inspection technology are explored.

/pdf/state-of-the-art-in-defect-detection-based-on-machine-vision-2rtzvgsnqy.pdf

State of the Art in Defect Detection Based on Machine Vision

Super-resolved structured illumination microscopy (SR-SIM) is an important tool for fluorescence microscopy. SR-SIM microscopes perform multiple image acquisitions with varying illumination patterns, and reconstruct them to a super-resolved image. In its most frequent, linear implementation, SR-SIM doubles the spatial resolution. The reconstruction is performed numerically on the acquired wide-field image data, and thus relies on a software implementation of specific SR-SIM image reconstruction algorithms. We present fairSIM, an easy-to-use plugin that provides SR-SIM reconstructions for a wide range of SR-SIM platforms directly within ImageJ. For research groups developing their own implementations of super-resolution structured illumination microscopy, fairSIM takes away the hurdle of generating yet another implementation of the reconstruction algorithm. For users of commercial microscopes, it offers an additional, in-depth analysis option for their data independent of specific operating systems. As a modular, open-source solution, fairSIM can easily be adapted, automated and extended as the field of SR-SIM progresses.

/pdf/open-source-image-reconstruction-of-super-resolution-2j3ywzesb5.pdf

Open-source image reconstruction of super-resolution structured illumination microscopy data in ImageJ

Structured illumination microscopy (SIM) allows rapid, super-resolution (SR) imaging in live specimens. We review recent technical advances in SR-SIM, with emphasis on imaging speed, resolution, and depth. Since its introduction decades ago, the technique has grown to offer myriad implementations, each with its own strengths and weaknesses. We discuss these, aiming to provide a practical guide for biologists and to highlight which approach is best suited to a given application.

Faster, sharper, and deeper: structured illumination microscopy for biological imaging.

pdf/micro-fourier-transform-profilometry-m-ftp-3d-shape-g72m4hoqvb.pdf

Micro Fourier Transform Profilometry ($μ$FTP): 3D shape measurement at 10,000 frames per second

Super-resolution three-dimensional (3D) optical microscopy has incomparable advantages over other high-resolution microscopic technologies, such as electron microscopy and atomic force microscopy, in the study of biological molecules, pathways and events in live cells and tissues. We present a novel approach of structured illumination microscopy (SIM) by using a digital micromirror device (DMD) for fringe projection and a low-coherence LED light for illumination. The lateral resolution of 90 nm and the optical sectioning depth of 120 μm were achieved. The maximum acquisition speed for 3D imaging in the optical sectioning mode was 1.6×107 pixels/second, which was mainly limited by the sensitivity and speed of the CCD camera. In contrast to other SIM techniques, the DMD-based LED-illumination SIM is cost-effective, ease of multi-wavelength switchable and speckle-noise-free. The 2D super-resolution and 3D optical sectioning modalities can be easily switched and applied to either fluorescent or non-fluorescent specimens.

https://kops.uni-konstanz.de/bitstream/handle/123456789/24786/Dan_247861.pdf?sequence=1

DMD-based LED-illumination Super-resolution and optical sectioning microscopy

Super-resolution three-dimensional (3D) optical microscopy has incomparable advantages over other high-resolution microscopic technologies, such as electron microscopy and atomic force microscopy, in the study of biological molecules, pathways and events in live cells and tissues. We present a novel approach of structured illumination microscopy (SIM) by using a digital micromirror device (DMD) for fringe projection and a low-coherence LED light for illumination. The lateral resolution of 90 nm and the optical sectioning depth of 120 mm were achieved. The maximum acquisition speed for 3D imaging in the optical sectioning mode was 1.6310 7 pixels/second, which was mainly limited by the sensitivity and speed of the CCD camera. In contrast to other SIM techniques, the DMD-based LED-illumination SIM is cost-effective, ease of multi-wavelength switchable and speckle-noise-free. The 2D super-resolution and 3D optical sectioning modalities can be easily switched and applied to either fluorescent or non-fluorescent specimens.

https://kops.uni-konstanz.de/bitstream/handle/123456789/24786/Dan_247861.pdf;sequence=1

DMD-based LED-illumination Super-resolution and optical sectioning

Handle everyday research tasks with reliable, citation-backed results

Your personal Research Agent to handle research tasks with citation-backed results

Popular Tasks used by Researchers

How can I help with your research?

Meet SciSpace

Get more enhanced response by uploading the PDFs you want me to reference.

No relevant PDFs in your library

SciSpace is the AI research assistant for academics. Run systematic literature reviews on 280M+ papers, and write papers with cited sources. Trusted by 1M+ students, PhDs & researchers.

SciSpace | AI for Research

Analyze PDFs

Code & Manuscripts

Funding & Grants

Literature & Patents

Medical & Clinical Data

Systematic Review

Visualize & Present

Web & Data

Build a Google Scholar-like website for your research.

Build a website

Create charts and images for your research

Create a Chart

Write a paper for submission to a journal

Draft a manuscript

Patent Search

Design eye-catching scientific posters in minutes.

Scientific Poster Generation

Systematic Literature Review

One task is running at the moment. Your messages will be shown right after.

Drag and drop or click here to browse

Loved by <highlight>1 million+</highlight> researchers

Extract a list of specific topics and their sources from unstructured text

Topics

Compare and analyze relevant papers that matches with your search

Papers

Get insights from PDFs and bookmarked papers from your library

My library

Recent searches

Try searching for:

Catch AI-generated content in scholarly and non-scholarly content

{ai} Detector

Ai Writer

Get PDF Summaries, highlighted text explanations 

Chat with PDF

Effortlessly create in-text citations and bibliographies in APA and 2,500 other formats

Citation generator

Get explanations, summaries, and answers on academic papers

Ease up your research workflow with {scispace}'s cohort of exciting AI tools

Elevate your academic writing skills and convey your ideas the way you want

Paraphraser

Explore our range of reading and writing tools

Your file is being prepared and should be ready in a few minutes. If it's a large file, it might take a bit longer. You can close this window, and we'll email you the file when it's done.

You have reached a maximum limit of <strong>{limit}</strong> columns in the table. Remove at least <strong>1</strong> column to add or create another one.

Liang Xia

Author Tools

Chat about Author

Papers

DMD-based LED-illumination Super-resolution and optical sectioning microscopy

DMD-based LED-illumination Super-resolution and optical sectioning