Super-resolution of wide-field infrared and low light level images using convolutional networks

2021 ◽  
Author(s):  
Yu-dan Chen ◽  
Gang LI ◽  
Fu-yu HUANG ◽  
He Liu
Keyword(s):  
Super Resolution ◽  
Light Level ◽  
Wide Field ◽  
Low Light ◽  
Convolutional Networks

scholarly journals Low-Light-Level Image Super-Resolution Reconstruction Based on a Multi-Scale Features Extraction Network

Photonics ◽  
2021 ◽  
Vol 8 (8) ◽  
pp. 321
Author(s):  
Bowen Wang ◽  
Yan Zou ◽  
Linfei Zhang ◽  
Yan Hu ◽  
Hao Yan ◽  
...  
Keyword(s):  
High Frequency ◽  
Signal To Noise Ratio ◽  
Super Resolution ◽  
Light Level ◽  
Superior Performance ◽  
Wide Field ◽  
Low Light ◽  
Color Mapping ◽  
Multi Scale ◽  
Imaging Sensors

Wide field-of-view (FOV) and high-resolution (HR) imaging are essential to many applications where high-content image acquisition is necessary. However, due to the insufficient spatial sampling of the image detector and the trade-off between pixel size and photosensitivity, the ability of current imaging sensors to obtain high spatial resolution is limited, especially under low-light-level (LLL) imaging conditions. To solve these problems, we propose a multi-scale feature extraction (MSFE) network to realize pixel-super-resolved LLL imaging. In order to perform data fusion and information extraction for low resolution (LR) images, the network extracts high-frequency detail information from different dimensions by combining the channel attention mechanism module and skip connection module. In this way, the calculation of the high-frequency components can receive greater attention. Compared with other networks, the peak signal-to-noise ratio of the reconstructed image was increased by 1.67 dB. Extensions of the MSFE network are investigated for scene-based color mapping of the gray image. Most of the color information could be recovered, and the similarity with the real image reached 0.728. The qualitative and quantitative experimental results show that the proposed method achieved superior performance in image fidelity and detail enhancement over the state-of-the-art.

Low-light-level image pixel super-resolution reconstruction method

2021 ◽  
Author(s):  
Bowen Wang ◽  
Ju Zhang ◽  
Ziheng Jin ◽  
Haojie Gu ◽  
Yan Zou ◽  
...  
Keyword(s):  
Super Resolution ◽  
Light Level ◽  
Reconstruction Method ◽  
Low Light

Software pattern recognition applied to nanodiffraction patterns from a STEM instrument

1986 ◽  
Vol 44 ◽  
pp. 694-695
Author(s):  
G.Y. Fan ◽  
J.M. Cowley
Keyword(s):  
Image Processing ◽  
Pattern Recognition ◽  
Computer Software ◽  
Processing System ◽  
Light Level ◽  
Host Computer ◽  
Low Light ◽  
Image Processing System ◽  
Recent Developments ◽  
On Line

In recent developments, the ASU HB5 has been modified so that the timing, positioning, and scanning of the finely focused electron probe can be entirely controlled by a host computer. This made the asynchronized handshake possible between the HB5 STEM and the image processing system which consists of host computer (PDP 11/34), DeAnza image processor (IP 5000) which is interfaced with a low-light level TV camera, array processor (AP 400) and various peripheral devices. This greatly facilitates the pattern recognition technique initiated by Monosmith and Cowley. Software called NANHB5 is under development which, instead of employing a set of photo-diodes to detect strong spots on a TV screen, uses various software techniques including on-line fast Fourier transform (FFT) to recognize patterns of greater complexity, taking advantage of the sophistication of our image processing system and the flexibility of computer software.

Low-light-level three-dimensional video microscope with long working distance objective lenses

1994 ◽  
Vol 52 ◽  
pp. 226-227
Author(s):  
W. Lin ◽  
J. Gregorio ◽  
T.J. Holmes ◽  
D. H. Szarowski ◽  
J.N. Turner
Keyword(s):  
Three Dimensional ◽  
Light Level ◽  
Stereo Pair ◽  
Light Illumination ◽  
Initial Image ◽  
Low Light ◽  
Image Recording ◽  
Depth Discrimination ◽  
Video Microscope ◽  
Working Distance

A low-light level video microscope with long working distance objective lenses has been built as part of our integrated three-dimensional (3-D) light microscopy workstation (Fig. 1). It allows the observation of living specimens under sufficiently low light illumination that no significant photobleaching or alternation of specimen physiology is produced. The improved image quality, depth discrimination and 3-D reconstruction provides a versatile intermediate resolution system that replaces the commonly used dissection microscope for initial image recording and positioning of microelectrodes for neurobiology. A 3-D image is displayed on-line to guide the execution of complex experiments. An image composed of 40 optical sections requires 7 minutes to process and display a stereo pair.The low-light level video microscope utilizes long working distance objective lenses from Mitutoyo (10X, 0.28NA, 37 mm working distance; 20X, 0.42NA, 20 mm working distance; 50X, 0.42NA, 20 mm working distance). They provide enough working distance to allow the placement of microelectrodes in the specimen.

scholarly journals Comparing Super-Resolution Microscopy Techniques to Analyze Chromosomes

2021 ◽  
Vol 22 (4) ◽  
pp. 1903
Author(s):  
Ivona Kubalová ◽  
Alžběta Němečková ◽  
Klaus Weisshart ◽  
Eva Hřibová ◽  
Veit Schubert
Keyword(s):  
Single Molecule ◽  
Imaging Techniques ◽  
Chromatin Condensation ◽  
Super Resolution ◽  
Stimulated Emission ◽  
Wide Field ◽  
Structured Illumination Microscopy ◽  
Metaphase Chromosomes ◽  
Localization Microscopy ◽  
Super Resolution Microscopy

The importance of fluorescence light microscopy for understanding cellular and sub-cellular structures and functions is undeniable. However, the resolution is limited by light diffraction (~200–250 nm laterally, ~500–700 nm axially). Meanwhile, super-resolution microscopy, such as structured illumination microscopy (SIM), is being applied more and more to overcome this restriction. Instead, super-resolution by stimulated emission depletion (STED) microscopy achieving a resolution of ~50 nm laterally and ~130 nm axially has not yet frequently been applied in plant cell research due to the required specific sample preparation and stable dye staining. Single-molecule localization microscopy (SMLM) including photoactivated localization microscopy (PALM) has not yet been widely used, although this nanoscopic technique allows even the detection of single molecules. In this study, we compared protein imaging within metaphase chromosomes of barley via conventional wide-field and confocal microscopy, and the sub-diffraction methods SIM, STED, and SMLM. The chromosomes were labeled by DAPI (4′,6-diamidino-2-phenylindol), a DNA-specific dye, and with antibodies against topoisomerase IIα (Topo II), a protein important for correct chromatin condensation. Compared to the diffraction-limited methods, the combination of the three different super-resolution imaging techniques delivered tremendous additional insights into the plant chromosome architecture through the achieved increased resolution.

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