Fast compressed sensing analysis for super-resolution imaging using L1-homotopy

被引:59
作者
Babcock, Hazen P. [1 ]
Moffitt, Jeffrey R. [1 ]
Cao, Yunlong [2 ]
Zhuang, Xiaowei [1 ]
机构
[1] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[2] Zhejiang Univ, Dept Phys, Hangzhou 310027, Peoples R China
来源
OPTICS EXPRESS | 2013年 / 21卷 / 23期
基金
美国国家卫生研究院;
关键词
OPTICAL RECONSTRUCTION MICROSCOPY; LOCALIZATION MICROSCOPY; LIVE CELLS; SPARSE; RESOLUTION; ALGORITHM; PROBES; STORM;
D O I
10.1364/OE.21.028583
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
In super-resolution imaging techniques based on single-molecule switching and localization, the time to acquire a super-resolution image is limited by the maximum density of fluorescent emitters that can be accurately localized per imaging frame. In order to increase the imaging rate, several methods have been recently developed to analyze images with higher emitter densities. One powerful approach uses methods based on compressed sensing to increase the analyzable emitter density per imaging frame by several-fold compared to other reported approaches. However, the computational cost of this approach, which uses interior point methods, is high, and analysis of a typical 40 mu m x 40 mu m field-of-view super-resolution movie requires thousands of hours on a high-end desktop personal computer. Here, we demonstrate an alternative compressed-sensing algorithm, L1-Homotopy (L1H), which can generate super-resolution image reconstructions that are essentially identical to those derived using interior point methods in one to two orders of magnitude less time depending on the emitter density. Moreover, for an experimental data set with varying emitter density, L1H analysis is similar to 300-fold faster than interior point methods. This drastic reduction in computational time should allow the compressed sensing approach to be routinely applied to super-resolution image analysis. (C) 2013 Optical Society of America
引用
收藏
页码:28583 / 28596
页数:14
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