Real-time correction of chromatic aberration in optical fluorescence microscopy.

IF 2.4 3区 化学 Q3 CHEMISTRY, ANALYTICAL
Ana Cayuela López, Pablo Conesa, Ana María Oña Blanco, José Antonio Gómez-Pedrero, Carlos Oscar S Sorzano
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引用次数: 1

Abstract

Multi-color fluorescence imaging is a powerful tool for studying the spatial relationships and interactions among sub-cellular structures in biological specimens. However, if improperly corrected, geometrical distortions caused by mechanical drift, refractive index mismatch, or chromatic aberration can lead to lower image resolution. In this paper, we present an extension of the image processing framework of Scipion by integrating a protocol called OFM Corrector, which corrects geometrical distortions in real-time using a B-spline-based elastic continuous registration technique. Our proposal provides a simple strategy to overcome chromatic aberration by digitally re-aligning color channels in multi-color fluorescence microscopy images, even in 3D or time. Our method relies on a geometrical calibration, which we do with fluorescent beads excited by different wavelengths of light and subsequently registered to get the elastic warp as a reference to correct chromatic shift. Our software is freely available with a user-friendly GUI and can be broadly used for various biological imaging problems. The paper presents a valuable tool for researchers working in light microscopy facilities.

光学荧光显微镜色差的实时校正。
多色荧光成像是研究生物标本中亚细胞结构间空间关系和相互作用的有力工具。然而,如果不正确的校正,几何畸变引起的机械漂移,折射率不匹配,或色差会导致较低的图像分辨率。在本文中,我们通过集成一个称为OFM校正器的协议,提出了Scipion图像处理框架的扩展,该协议使用基于b样条的弹性连续配准技术实时校正几何畸变。我们的建议提供了一种简单的策略,通过数字重新对齐多色荧光显微镜图像中的颜色通道来克服色差,即使在3D或时间中也是如此。我们的方法依赖于几何校准,我们用荧光珠被不同波长的光激发并随后注册以获得弹性翘曲作为校正色差的参考。我们的软件是免费提供的,具有用户友好的GUI,可广泛用于各种生物成像问题。本文为在光学显微镜设备中工作的研究人员提供了一个有价值的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Methods and Applications in Fluorescence
Methods and Applications in Fluorescence CHEMISTRY, ANALYTICALCHEMISTRY, PHYSICAL&n-CHEMISTRY, PHYSICAL
CiteScore
6.20
自引率
3.10%
发文量
60
期刊介绍: Methods and Applications in Fluorescence focuses on new developments in fluorescence spectroscopy, imaging, microscopy, fluorescent probes, labels and (nano)materials. It will feature both methods and advanced (bio)applications and accepts original research articles, reviews and technical notes.
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