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Simultaneous decomposition of multiple retinal pigment epithelium (RPE) autofluorescence hyperspectral datasets for fluorophor discovery

机译:同时分解多个用于荧光团发现的视网膜色素上皮(RPE)自发荧光高光谱数据集

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?Purpose?Excitation of RPE autofluorescence with different wavelengths produces different but closely related spectral data. We hypothesized that simultaneous decomposition of multiple hyperspectral datasets into major spectral signatures and their spatial distributions with non negative matrix factorization (NMF) could exploit these relationships to recover results superior to factoring any single hypercube.?Methods?Pure RPE/BrM flat mounts were separately excited at 436-460nm and 480-510nm and hyperspectral emission data were captured by methods described in detail by Johri and Agarwal abstracts. Standard NMF factors a hypercube A into the product of matrices W and H (Fig 1a), where W is the spectra of the recovered sources and H carries their spatial localizations (abundance images). In our formulation, we always retrieve 4 spectral signatures for RPE and one for BrM. We paired each signal found at 436nm excitation to its corresponding signal at 480nm, and linked the two datasets by requiring that the spatial localizations of the paired signals must be exactly the same, because they come from the same compound. (Fig 1b)?Results?Fig. 2 (a, b) shows the 5 spectra recovered from the fovea of a 34 y/o female donor at 436nm and 480nm with standard NMF. The spectra are clearly paired according to the emission maxima. Fig 2c shows the results when the data are decomposed simultaneously: 10 abundant spectra are clearly paired in shape and location, suggesting single species. Each pair corresponds to one clearly defined abundance image.?Conclusions?Simultaneous decomposition of multiple RPE hyperspectral datasets is superior to standard NMF at breaking down a complex spectrum representing a mixture of fluorophors into its individual spectral signals, hence providing better candidates for biochemical identification. ?View OriginalDownload SlideView OriginalDownload Slide?View OriginalDownload SlideView OriginalDownload Slide? Keywords: 701 retinal pigment epithelium ? 551 imaging/image analysis: non-clinical ? 582 ipofuscin ?.
机译:目的激发不同波长的RPE自发荧光会产生不同但密切相关的光谱数据。我们假设使用非负矩阵分解(NMF)将多个高光谱数据集同时分解为主要的光谱特征及其空间分布可以利用这些关系来恢复优于分解任何单个超立方体的结果。 Johri和Agarwal摘要详细描述的方法捕获了在436-460nm和480-510nm处激发的光和高光谱发射数据。标准NMF将超立方体A分解为矩阵W和H的乘积(图1a),其中W是回收源的光谱,H携带其空间定位(丰度图像)。在我们的公式中,我们总是为RPE检索4个光谱特征,为BrM检索一个特征。我们将在436nm激发下找到的每个信号与在480nm处对应的信号配对,并通过要求配对信号的空间定位必须完全相同来链接两个数据集,因为它们来自同一化合物。 (图1b)?结果?图2(a,b)显示了用标准NMF在436nm和480nm下从34y / o雌性供体的中央凹处回收的5个光谱。光谱根据发射最大值明确配对。图2c显示了同时分解数据时的结果:10个丰富的光谱在形状和位置上清楚地配对,表明是单个物种。每对对应一个清晰定义的丰度图像。结论:多个RPE高光谱数据集的同时分解在将代表荧光团混合物的复杂光谱分解成其单个光谱信号方面优于标准NMF,从而为生化识别提供了更好的候选者。查看原始下载幻灯片查看原始下载幻灯片查看原始下载幻灯片查看原始下载幻灯片关键词:701视网膜色素上皮? 551成像/图像分析:非临床第582章

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