3D biological object detection and labeling in multidimensional microscopy imaging

Juhui Wang, A. Trubuil, C. Graffigne
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引用次数: 3

Abstract

One essential assumption used in object detection and labeling by imaging is that the photometric properties of the object are homogeneous. This homogeneity requirement is often violated in microscopy imaging. Classical methods are usually of high computational cost and fail to give a stable solution. This paper presents a low computational complexity and robust method for 3D biological object detection and labeling. The developed approach is based on a statistical, non-parametric framework. The image is first divided into regular non-overlapped regions and each region is evaluated according to a general photometric variability model. The regions not consistent with this model are considered as aberrations in the data and excluded from the analysis procedure. Simultaneously, the interior parts of the object are detected. They correspond to regions where the supposed model is valid. In the second stage, the valid regions from the same object are merged under a set of hypotheses. These hypotheses are generated by taking into account photometric and geometric properties of objects and the merging is realized according to an iterative algorithm. The approach has been applied in investigations of the spatial distribution of nuclei on colonic glands of rats observed with with help of confocal fluorescence microscopy.
三维生物目标检测和标记在多维显微镜成像
在物体检测和标记成像中使用的一个基本假设是物体的光度特性是均匀的。这种均匀性要求在显微镜成像中经常被违反。经典方法通常计算成本高,且不能给出稳定的解。提出了一种计算复杂度低、鲁棒性好的三维生物目标检测与标记方法。开发的方法是基于统计的非参数框架。首先将图像划分为规则的非重叠区域,并根据一般的光度变异性模型对每个区域进行评估。与该模型不一致的区域被认为是数据中的畸变,并被排除在分析程序之外。同时,检测物体的内部部分。它们对应于假定的模型有效的区域。在第二阶段,将同一目标的有效区域合并到一组假设下。这些假设是通过考虑物体的光度和几何特性产生的,并通过迭代算法实现合并。该方法已应用于共聚焦荧光显微镜观察大鼠结肠腺细胞核的空间分布。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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