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Application of principal component analysis to multispectral-multimodal optical image analysis for malaria diagnostics

机译:主成分分析在疟疾诊断多光谱多峰光学图像分析中的应用

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Background Multispectral imaging microscopy is a novel microscopic technique that integrates spectroscopy with optical imaging to record both spectral and spatial information of a specimen. This enables acquisition of a large and more informative dataset than is achievable in conventional optical microscopy. However, such data are characterized by high signal correlation and are difficult to interpret using univariate data analysis techniques. Methods In this work, the development and application of a novel method which uses principal component analysis (PCA) in the processing of spectral images obtained from a simple multispectral-multimodal imaging microscope to detect Plasmodium parasites in unstained thin blood smear for malaria diagnostics is reported. The optical microscope used in this work has been modified by replacing the broadband light source (tungsten halogen lamp) with a set of light emitting diodes (LEDs) emitting thirteen different wavelengths of monochromatic light in the UV–vis-NIR range. The LEDs are activated sequentially to illuminate same spot of the unstained thin blood smears on glass slides, and grey level images are recorded at each wavelength. PCA was used to perform data dimensionality reduction and to enhance score images for visualization as well as for feature extraction through clusters in score space. Results Using this approach, haemozoin was uniquely distinguished from haemoglobin in unstained thin blood smears on glass slides and the 590–700 spectral range identified as an important band for optical imaging of haemozoin as a biomarker for malaria diagnosis. Conclusion This work is of great significance in reducing the time spent on staining malaria specimens and thus drastically reducing diagnosis time duration. The approach has the potential of replacing a trained human eye with a trained computerized vision system for malaria parasite blood screening.
机译:背景技术多光谱成像显微镜是一种新颖的显微技术,其将光谱学与光学成像相结合以记录标本的光谱和空间信息。与传统的光学显微镜相比,这可以获取更大且信息量更大的数据集。但是,此类数据的特征在于信号相关性高,并且难以使用单变量数据分析技术来解释。方法在这项工作中,报道了一种新方法的开发和应用,该方法使用主成分分析(PCA)处理从简单的多光谱多峰成像显微镜获得的光谱图像以检测未染色的薄血涂片中的疟原虫用于疟疾诊断。这项工作中使用的光学显微镜已经进行了修改,用一组发光二极管(LED)代替了宽带光源(卤钨灯),这些发光二极管发出13种不同波长的紫外可见近红外波长。依次激活LED,以照亮载玻片上未染色的薄血涂片的相同点,并在每个波长下记录灰度图像。 PCA用于执行数据降维和增强得分图像以进行可视化以及通过得分空间中的聚类进行特征提取。结果使用这种方法,在载玻片上未染色的薄血涂片中,血红蛋白与血红蛋白有着独特的区别,并且590-700光谱范围被确定为血红蛋白光学成像的重要谱带,可作为疟疾诊断的生物标记。结论这项工作对减少疟疾标本的染色时间并因此大大缩短诊断时间具有重要意义。该方法具有用受过训练的计算机视觉系统代替受过训练的人眼进行疟疾寄生虫血液筛查的潜力。

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