ArticleBiomedical optics express2017
Line-scanning hyperspectral imaging based on structured illumination optical sectioning.
Article in Biomedical optics express, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
6 citing papers in PubMed.
- Hyperspectral Imaging (HSI) for meat quality evaluation across the supply chain: Current and future trends.Current research in food science · 2022Review
- Snapshot hyperspectral light field tomography.Optica · 2021Article
- DMD-based hyperspectral microscopy with flexible multiline parallel scanning.Microsystems & nanoengineering · 2021Article
- Development of a fast calibration method for image mapping spectrometry.Applied optics · 2020Article
- Comparing mapping and direct hyperspectral imaging in stand-off Raman spectroscopy for remote material identification.Journal of Raman spectroscopy : JRS · 2019Article
- Optimization of wavelength selection for multispectral image acquisition: a case study of atrial ablation lesions.Biomedical optics express · 2018Article
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Line-scanning hyperspectral imaging (LHSI) is known to have a higher acquisition rate but lower sectioning capability than point-scanning hyperspectral imaging. To further increase the axial imaging contrast of LHSI, structured illumination was integrated into line excitation to remove the off-focus and scattered on-focus fluorescence signals. In an unsectioned leaf, the imaging contrast can be enhanced by 8 times, while in sectioned mouse skin tissues, a 4.5-fold enhancement can be achieved. With a spectral resolution of 1.15 nm, the fluorophores with seriously-overlapped spectra was proved to be separated without cross-talk by applying linear unmixing to the recorded spectral information.
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Registered trials
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