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Continuous localization using sparsity constraints for high-density super-resolution microscopy

机译:使用稀疏约束连续定位用于高密度超分辨率显微镜

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Super-resolution localization microscopy relies on sparse activation of photo-switchable probes. Such activation, however, introduces limited temporal resolution. High-density imaging overcomes this limitation by allowing several neighboring probes to be activated simultaneously. In this work, we propose an algorithm that incorporates a continuous-domain sparsity prior into the high-density localization problem. We use a Taylor approximation of the PSF, and rely on a fast proximal gradient optimization procedure. Unlike currently available methods that use discrete-domain sparsity priors, our approach does not restrict the estimated locations to a pre-defined sampling grid. Experimental results of simulated and real data demonstrate significant improvement over these methods in terms of accuracy, molecular identification and computational complexity.
机译:超分辨率定位显微镜依靠光开关探针的稀疏激活。然而,这种激活引入了有限的时间分辨率。高密度成像通过允许同时激活几个相邻的探针来克服此限制。在这项工作中,我们提出了一种算法,该算法将连续域稀疏性合并到高密度本地化问题中。我们使用PSF的泰勒(Taylor)近似,并依靠快速的近端梯度优化过程。与当前使用离散域稀疏先验的方法不同,我们的方法不会将估计的位置限制为预定义的采样网格。模拟和真实数据的实验结果表明,在准确性,分子识别和计算复杂度方面,这些方法均取得了显着改进。

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