PerfectlyAverage:一种经典的开源软件方法,用于确定激光扫描荧光显微镜的最佳平均参数。

IF 1.5 4区 工程技术 Q3 MICROSCOPY
S Foylan, L M Rooney, W B Amos, G W Gould, G McConnell
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引用次数: 0

摘要

激光扫描荧光显微镜(LSFM)是一种应用广泛的成像方法,但图像质量经常受到噪声的影响。平均技术可以提高信噪比(SNR),但虽然这可以提高图像质量,但过多的帧积累可能会引入光漂白,并可能导致不必要的长采集时间。提出了一种称为PerfectlyAverage的经典软件方法,用于使用信噪比、光漂白和功率谱密度(PSD)测量来确定LSFM中平均的最佳帧数。通过评估时间序列中帧间的时间强度变化,perfeclyaverage识别出额外平均不再提供显著降噪的点。用荧光染色的纸巾和成纤维细胞进行的实验验证了该方法,表明平均时间最多可减少四倍。perfeclyaverage是开源的,与任何LSFM数据兼容,它旨在改善成像工作流程,同时减少对选择平均值数量的主观标准的依赖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PerfectlyAverage: A classical open-source software method to determine the optimal averaging parameters in laser scanning fluorescence microscopy.

Laser scanning fluorescence microscopy (LSFM) is a widely used imaging method, but image quality is often degraded by noise. Averaging techniques can enhance the signal-to-noise ratio (SNR), but while this can improve image quality, excessive frame accumulation can introduce photobleaching and may lead to unnecessarily long acquisition times. A classical software method called PerfectlyAverage is presented to determine the optimal number of frames for averaging in LSFM using SNR, photobleaching, and power spectral density (PSD) measurements. By assessing temporal intensity variations across frames in a time series, PerfectlyAverage identifies the point where additional averaging ceases to provide significant noise reduction. Experiments with fluorescently stained tissue paper and fibroblast cells validated the approach, demonstrating that up to a fourfold reduction in averaging time may be possible. PerfectlyAverage is open source, compatible with any LSFM data, and it is aimed at improving imaging workflows while reducing the reliance on subjective criteria for choosing the number of averages.

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来源期刊
Journal of microscopy
Journal of microscopy 工程技术-显微镜技术
CiteScore
4.30
自引率
5.00%
发文量
83
审稿时长
1 months
期刊介绍: The Journal of Microscopy is the oldest journal dedicated to the science of microscopy and the only peer-reviewed publication of the Royal Microscopical Society. It publishes papers that report on the very latest developments in microscopy such as advances in microscopy techniques or novel areas of application. The Journal does not seek to publish routine applications of microscopy or specimen preparation even though the submission may otherwise have a high scientific merit. The scope covers research in the physical and biological sciences and covers imaging methods using light, electrons, X-rays and other radiations as well as atomic force and near field techniques. Interdisciplinary research is welcome. Papers pertaining to microscopy are also welcomed on optical theory, spectroscopy, novel specimen preparation and manipulation methods and image recording, processing and analysis including dynamic analysis of living specimens. Publication types include full papers, hot topic fast tracked communications and review articles. Authors considering submitting a review article should contact the editorial office first.
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