Harms H, Aus H M
Cytometry. 1984 May;5(3):228-35. doi: 10.1002/cyto.990050303.
The basic postulate of this paper is that the commonly accepted sampling density of 2-4 pixels/micron in a high-resolution TV microscope system is too low to digitize exactly and analyze the complex cellular detail found in stained cell images. Depending on the specific microscope system, the required sampling density is much higher, lying between 15 and 30 pixels/micron. This sampling density is derived from the aliasing error, the resolution loss, and computational limitations. The mathematical and optical methods and equipment used to obtain these results are described in detail.
本文的基本假设是,在高分辨率电视显微镜系统中,普遍接受的2-4像素/微米的采样密度过低,无法精确数字化并分析染色细胞图像中发现的复杂细胞细节。根据具体的显微镜系统,所需的采样密度要高得多,介于15至30像素/微米之间。这个采样密度是由混叠误差、分辨率损失和计算限制得出的。详细描述了用于获得这些结果的数学和光学方法及设备。