A Fuzzy Algorithm to Trace Stained Neurons in Serial Block-Face Scanning Electron Microscopy Image Series

K. Saetzler, P. McCanny, E. P. Rodriguez, H. Horstmann, R. M. Bruno, W. Denk
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引用次数: 3

Abstract

With the recently developed serial block-face scanning electron microscope (SBFSEM) it is now possible to analyze the 3-D structure of biological specimens at a resolution that is one order of magnitude better compared to light microscopy requiring minimal user input. It allows the automatic creation of large series (≫ 1000) of digitally imaged ultra-thin sections (≪ 100 nm) from heavy metal-stained and plastic embedded tissue. Together with the ability of selectively staining individual, identified neurons using electron dense material one can visually track the complete structure at a resolution as low as 20x20x40 nm. Here we introduce a simple fuzzy region-growing tracing algorithm that incorporates a minimum of prior knowledge about object and background gray level distributions. We show that this algorithm reliably traces structures of interest over several hundreds of sections opening the unique opportunity to systematically study the morphology of neuronal structures at the nanometre scale in a fully automated way.
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块脸扫描电镜图像序列中染色神经元的模糊跟踪算法
随着最近开发的串行块面扫描电子显微镜(sfsem),现在可以分析生物标本的三维结构,其分辨率比光学显微镜好一个数量级,需要最少的用户输入。它可以从沾有重金属和塑料的组织中自动生成大系列(< 1000)的数字成像超薄切片(< 100 nm)。再加上选择性染色单个神经元的能力,使用电子密集材料可以在低至20x20x40nm的分辨率下直观地跟踪完整的结构。本文介绍了一种简单的模糊区域增长跟踪算法,该算法结合了关于目标和背景灰度分布的最小先验知识。我们表明,该算法可靠地追踪了数百个部分的感兴趣结构,为以全自动方式系统地研究纳米尺度神经元结构的形态提供了独特的机会。
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