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无偏全局聚类参数选择用于单分子定位显微镜。

Unbiased choice of global clustering parameters for single-molecule localization microscopy.

机构信息

Institute of Experimental Epileptology and Cognition Research, University of Bonn Medical Center, Bonn, Germany.

Theory of Neural Dynamics Group, Max Planck Institute for Brain Research, Frankfurt, Germany.

出版信息

Sci Rep. 2022 Dec 29;12(1):22561. doi: 10.1038/s41598-022-27074-1.

Abstract

Single-molecule localization microscopy resolves objects below the diffraction limit of light via sparse, stochastic detection of target molecules. Single molecules appear as clustered detection events after image reconstruction. However, identification of clusters of localizations is often complicated by the spatial proximity of target molecules and by background noise. Clustering results of existing algorithms often depend on user-generated training data or user-selected parameters, which can lead to unintentional clustering errors. Here we suggest an unbiased algorithm (FINDER) based on adaptive global parameter selection and demonstrate that the algorithm is robust to noise inclusion and target molecule density. We benchmarked FINDER against the most common density based clustering algorithms in test scenarios based on experimental datasets. We show that FINDER can keep the number of false positive inclusions low while also maintaining a low number of false negative detections in densely populated regions.

摘要

单分子定位显微镜通过稀疏、随机的目标分子检测,突破了光的衍射极限分辨率来解析物体。在图像重建后,单个分子表现为聚集的检测事件。然而,由于目标分子的空间接近和背景噪声,聚类的结果往往很复杂。现有的聚类算法的结果往往取决于用户生成的训练数据或用户选择的参数,这可能导致无意的聚类错误。在这里,我们提出了一种基于自适应全局参数选择的无偏算法(FINDER),并证明该算法对噪声包含和目标分子密度具有鲁棒性。我们在基于实验数据集的测试场景中,将 FINDER 与最常见的基于密度的聚类算法进行了基准测试。我们表明,FINDER 可以在保持低误报率的同时,在密集区域也保持低漏检率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5c9/9800574/848f2f0f9d74/41598_2022_27074_Fig1_HTML.jpg

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