Bouyssoux Alexandre, Jarnouen Kathleen, Lallement Laetitia, Fezzani Riadh, Olivo-Marin Jean-Christophe
BioImage Analysis Unit, CNRS UMR 3691, Institut Pasteur, Université de Paris, Paris, France.
VitaDX International, Paris, France.
Cytometry A. 2022 Dec;101(12):1068-1083. doi: 10.1002/cyto.a.24659. Epub 2022 Jun 18.
The progress of digital pathology in recent years has been an opportunity for the development of automated image analysis algorithms for quantitative measurements and computer aided diagnosis. With those new methods comes the need for high staining quality and reproducibility, as image analysis tools are typically more sensible to slight stain variations than trained pathologists. This article presents a method for the automated analysis of cytology slides stains specifically adapted to the challenges encountered in digital cytopathology. In particular, the variety of cell types in cytology slides, the 3D distribution of the cellular material, the presence of superposed cells and the need for independent analysis of sub-cellular compartments are addressed. The proposed method is applied to the quantification of staining variations for quality control, resulting from changes in the staining protocol such as reagent immersion time or a reagent change. Another demonstrated application is the selection of staining protocol parameters that maximize the visible details in nucleus. Finally the analysis pipeline is also used to compare different stain normalization algorithms on digital cytology slides. Code available at: https://gitlab.com/vitadx/articles/automated_staining_analysis.
近年来,数字病理学的进展为开发用于定量测量和计算机辅助诊断的自动图像分析算法提供了契机。随着这些新方法的出现,对高染色质量和可重复性的需求也随之而来,因为图像分析工具通常比训练有素的病理学家对轻微的染色变化更敏感。本文提出了一种专门针对数字细胞病理学中遇到的挑战而设计的细胞学载玻片染色自动分析方法。特别是,解决了细胞学载玻片中细胞类型的多样性、细胞物质的三维分布、叠加细胞的存在以及对亚细胞区室进行独立分析的需求。所提出的方法应用于染色变化的定量分析,以进行质量控制,这些变化是由染色方案的改变引起的,如试剂浸泡时间或试剂更换。另一个已证明的应用是选择能使细胞核中可见细节最大化的染色方案参数。最后,分析流程还用于比较数字细胞学载玻片上不同的染色归一化算法。代码可在以下网址获取:https://gitlab.com/vitadx/articles/automated_staining_analysis 。