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Fast4DReg - 快速注册 4D 显微镜数据集。

Fast4DReg - fast registration of 4D microscopy datasets.

机构信息

Åbo Akademi University, Faculty of Science and Engineering, Biosciences, Turku 20520, Finland.

Turku Bioimaging, University of Turku and Åbo Akademi University, Turku 20520, Finland.

出版信息

J Cell Sci. 2023 Feb 15;136(4). doi: 10.1242/jcs.260728. Epub 2023 Feb 23.

Abstract

Unwanted sample drift is a common issue that plagues microscopy experiments, preventing accurate temporal visualization and quantification of biological processes. Although multiple methods and tools exist to correct images post acquisition, performing drift correction of three-dimensional (3D) videos using open-source solutions remains challenging and time consuming. Here, we present a new tool developed for ImageJ or Fiji called Fast4DReg that can quickly correct axial and lateral drift in 3D video-microscopy datasets. Fast4DReg works by creating intensity projections along multiple axes and estimating the drift between frames using two-dimensional cross-correlations. Using synthetic and acquired datasets, we demonstrate that Fast4DReg can perform better than other state-of-the-art open-source drift-correction tools and significantly outperforms them in speed. We also demonstrate that Fast4DReg can be used to register misaligned channels in 3D using either calibration slides or misaligned images directly. Altogether, Fast4DReg provides a quick and easy-to-use method to correct 3D imaging data before further visualization and analysis.

摘要

非期望样本漂移是困扰显微镜实验的一个常见问题,它会妨碍对生物过程进行准确的时间可视化和定量分析。尽管存在多种方法和工具可用于在获取后校正图像,但使用开源解决方案对三维 (3D) 视频执行漂移校正仍然具有挑战性且耗时。在这里,我们提出了一种新的工具,名为 Fast4DReg,它可用于 ImageJ 或 Fiji,可快速校正 3D 视频显微镜数据集的轴向和侧向漂移。Fast4DReg 通过沿着多个轴创建强度投影并使用二维互相关来估计帧之间的漂移来工作。使用合成和获取的数据集,我们证明了 Fast4DReg 可以比其他最先进的开源漂移校正工具表现更好,并且在速度上明显优于它们。我们还证明了 Fast4DReg 可以用于使用校准幻灯片或直接使用未对准的图像在 3D 中注册未对准的通道。总的来说,Fast4DReg 提供了一种快速易用的方法,可以在进一步可视化和分析之前校正 3D 成像数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a94b/10022679/367eec8064df/joces-136-260728-g1.jpg

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