Open-source image reconstruction of super-resolution structured illumination microscopy data in ImageJ

被引:217
作者
Mueller, Marcel [1 ]
Moenkemoeller, Viola [1 ]
Hennig, Simon [1 ]
Huebner, Wolfgang [1 ]
Huser, Thomas [1 ,2 ,3 ]
机构
[1] Univ Bielefeld, Dept Phys, Biomol Photon, D-33615 Bielefeld, Germany
[2] Univ Calif Davis, Dept Internal Med, Sacramento, CA 95817 USA
[3] Univ Calif Davis, NSF Ctr Biophoton, Sacramento, CA 95817 USA
来源
NATURE COMMUNICATIONS | 2016年 / 7卷
关键词
PHASE-SHIFT ESTIMATION; FLUORESCENCE MICROSCOPY; EXCITATION MICROSCOPY; LIVE CELLS; RESOLUTION; SOFTWARE; LIMIT; SIM;
D O I
10.1038/ncomms10980
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Super-resolved structured illumination microscopy (SR-SIM) is an important tool for fluorescence microscopy. SR-SIM microscopes perform multiple image acquisitions with varying illumination patterns, and reconstruct them to a super-resolved image. In its most frequent, linear implementation, SR-SIM doubles the spatial resolution. The reconstruction is performed numerically on the acquired wide-field image data, and thus relies on a software implementation of specific SR-SIM image reconstruction algorithms. We present fairSIM, an easy-to-use plugin that provides SR-SIM reconstructions for a wide range of SR-SIM platforms directly within ImageJ. For research groups developing their own implementations of super-resolution structured illumination microscopy, fairSIM takes away the hurdle of generating yet another implementation of the reconstruction algorithm. For users of commercial microscopes, it offers an additional, in-depth analysis option for their data independent of specific operating systems. As a modular, open-source solution, fairSIM can easily be adapted, automated and extended as the field of SR-SIM progresses.
引用
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页数:6
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