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Reliable Cell Segmentation Based on Spectral Phasor Analysis of Hyperspectral Stimulated Raman Scattering Imaging Data

机译:基于光谱相量分析的高光谱受激拉曼散射成像数据的可靠细胞分割

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Hyperspectral stimulated Raman scattering (SRS) imaging has rapidly become an emerging tool for high content analyses of cell and tissue systems. The label-free nature of SRS imaging combined with its chemical specificity allows in situ and in vivo biochemical quantification at submicrometer resolution without sectioning and staining. Current hyperspectral SRS data analysis methods are based on either linear unmixing or multivariate analysis, which are not sensitive to small spectral variations and often provide obscure information on the cell composition. Here, we demonstrate a spectral phasor analysis method that allows fast and reliable cellular organelle segmentation of mammalian cells, without any a priori knowledge of their composition or basis spectra. We further show that, in combination with a branch-bound algorithm for optimal selection of a few wavenumbers, spectral phasor analysis provides a robust solution to label-free single cell analysis.
机译:高光谱激发拉曼散射(SRS)成像已迅速成为对细胞和组织系统进行高含量分析的新兴工具。 SRS成像的无标签性质及其化学特异性可实现亚微米分辨率的原位和体内生化定量分析,而无需切片和染色。当前的高光谱SRS数据分析方法基于线性分解或多变量分析,这些方法对微小的光谱变化不敏感,并且通常会提供有关细胞组成的模糊信息。在这里,我们展示了一种频谱相量分析方法,该方法可以对哺乳动物细胞进行快速可靠的细胞器分割,而无需对其成分或基础光谱有任何先验知识。我们进一步表明,结合用于某些波数的最佳选择的分支约束算法,频谱相量分析为无标记单细胞分析提供了可靠的解决方案。

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