基于无模型机器学习的3D单分子定位显微镜。

IF 1.9 4区 工程技术 Q3 MICROSCOPY
Miguel A. Boland, Jonathan P. E. Lightley, Edwin Garcia, Sunil Kumar, Chris Dunsby, Seth Flaxman, Mark A. A. Neil, Paul M. W. French, Edward A. K. Cohen
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引用次数: 0

摘要

单分子定位显微镜(SMLM)可以提供来自传统荧光显微镜的二维超分辨率图像数据,而三维(3D) SMLM通常涉及对显微镜的修改,例如,在点扩散函数中设计可预测的轴向变化。在这里,我们展示了一种3D SMLM方法(我们称之为“easyZloc”),它利用了一种轻量级的卷积神经网络,这种神经网络通常适用,包括“标准”(未经修改)荧光显微镜,我们认为这在高通量SMLM工作流程中可能是实用的。我们证明了核孔复合物的重建具有与先前报道的方法相当的性能,但在计算能力和执行时间上显着降低。三维重建的核膜和肌动蛋白样品在更大的轴向范围内也显示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Model-free machine learning-based 3D single molecule localisation microscopy

Model-free machine learning-based 3D single molecule localisation microscopy

Single molecule localisation microscopy (SMLM) can provide two-dimensional super-resolved image data from conventional fluorescence microscopes, while three dimensional (3D) SMLM usually involves a modification of the microscope, for example, to engineer a predictable axial variation in the point spread function. Here we demonstrate a 3D SMLM approach (we call ‘easyZloc') utilising a lightweight Convolutional Neural Network that is generally applicable, including with ‘standard’ (unmodified) fluorescence microscopes, and which we consider may be practically useful in a high throughput SMLM workflow. We demonstrate the reconstruction of nuclear pore complexes with comparable performance to previously reported methods but with a significant reduction in computational power and execution time. 3D reconstructions of the nuclear envelope and an actin sample over a larger axial range are also shown.

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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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