GraspJ: An open source, real-time analysis package for super-resolution imaging

被引:0
作者
Brede, Norman [1 ,2 ]
Lakadamyali, Melike [2 ]
机构
[1] Department of Physics and Astronomy, University of Heidelberg, Heidelberg
[2] ICFO-Institut de Ciències Fotòniques, Mediterranean Technology Park, Castelldefels (Barcelona)
关键词
GPU; Maximum likelihood; PALM; STORM;
D O I
10.1186/2192-2853-1-11
中图分类号
学科分类号
摘要
We present an open source, real-time data analysis and rendering tool for super-resolution imaging techniques that are based on single molecule detection and localization (e. g. stochastic optical reconstruction microscopy - STORM and photoactivation localization microscopy - PALM). The recent availability of commercial STORM and PALM microscopes has made these techniques accessible to a wide range of researchers. However, the availability of high speed data analysis and rendering software lags behind, requiring researchers to develop their own analysis platforms or rely on commercial ones. We implemented GraspJ (GPU-Run Analysis for STORM and PALM), an ImageJ plug-in with a convenient user interface, that allows high accuracy localization of single molecules as well as processing and rendering of high resolution images in real-time. GraspJ includes several features such as drift correction, multi-color, 3D analysis/rendering, and is compatible with a large range of data acquisition software. In addition, it allows easy interfacing with other image processing tools available with ImageJ. Overall we believe that GraspJ will be a valuable tool for the super-resolution imaging field. © 2012 Brede and Lakadamyali.
引用
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页码:1 / 7
页数:6
相关论文
共 28 条
[1]  
Hell S.W., Far-field optical nanoscopy, Science, 316, (2007)
[2]  
Bates M., Huang B., Zhuang X., Super-resolution microscopy by nanoscale localization of photo-switchable fluorescent probes, Curr Opin Chem Biol, 12, (2008)
[3]  
Fernandez-Suarez M., Ting A.Y., Fluorescent probes for super-resolution imaging in living cells, Nat Rev Mol Cell Biol, 9, (2008)
[4]  
Patterson G., Davidson M., Manley S., Lippincott-Schwartz J., Superresolution imaging using single-molecule localization, Annu Rev Phys Chem, 61, (2010)
[5]  
Dempsey G.T., Vaughan J.C., Chen K.H., Bates M., Zhuang X., Evaluation of fluorophores for optimal performance in localization-based super-resolution imaging, Nat Methods, 8, (2011)
[6]  
Bates M., Huang B., Dempsey G.T., Zhuang X., Multicolor super-resolution imaging with photo-switchable fluorescent probes, Science, 317, (2007)
[7]  
Rust M.J., Bates M., Zhuang X., Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM), Nat Methods, 3, (2006)
[8]  
Betzig E., Patterson G.H., Sougrat R., Lindwasser O.W., Olenych S., Bonifacino J.S., Davidson M.W., Lippincott-Schwartz J., Hess H.F., Imaging intracellular fluorescent proteins at nanometer resolution, Science, 313, (2006)
[9]  
Smith C.S., Joseph N., Rieger B., Lidke K.A., Fast, single-molecule localization that achieves theoretically minimum uncertainty, Nat Methods, 7, (2010)
[10]  
Wolter S., Schuttpelz M., Tscherepanow M., van de Linde S., Heilemann M., Sauer M., Real-time computation of subdiffraction-resolution fluorescence images, J Microsc, 237, (2010)