High density molecule localization for super-resolution microscopy using CEL0 based sparse approximation

S. Gazagnes, Emmanuel Soubies, L. Blanc-Féraud
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引用次数: 43

Abstract

Single molecule localization microscopy has made great improvements in spatial resolution achieving performance beyond the diffraction limit by sequentially activating and imaging small subsets of molecules. Here, we present an algorithm designed for high-density molecule localization which is of a major importance in order to improve the temporal resolution of such microscopy techniques. We formulate the localization problem as a sparse approximation problem which is then relaxed using the recently proposed CEL0 penalty, allowing an optimization through recent nonsmooth nonconvex algorithms. Finally, performances of the proposed method are compared with one of the best current method for high-density molecules localization on simulated and real data.
基于CEL0稀疏近似的超分辨显微镜高密度分子定位
单分子定位显微镜在空间分辨率方面取得了很大的进步,通过顺序激活和成像小分子子集,实现了超越衍射极限的性能。在这里,我们提出了一种高密度分子定位算法,这对于提高此类显微镜技术的时间分辨率至关重要。我们将定位问题表述为一个稀疏逼近问题,然后使用最近提出的CEL0惩罚进行放松,允许通过最近的非光滑非凸算法进行优化。最后,在模拟数据和实际数据上,将该方法与目前最优的高密度分子定位方法进行了性能比较。
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