管道(软件)
生物
计算生物学
分割
转录组
计算机科学
空间分析
下游(制造业)
生物信息学
流线、条纹线和路径线
表达式(计算机科学)
图像分辨率
数据挖掘
人工智能
高分辨率
肿瘤异质性
图像分割
基因表达谱
系统生物学
基因组学
肿瘤微环境
作者
Kristi Ajazi,Massimiliano Volpe,Johannes Roylands,Jason Krogh-Pedersen,Kristian Pietras,Lennart Greiff,Malin Lindstedt
摘要
Spatial transcriptomics enables researchers to study gene expression within tumor microenvironments at single-cell resolution while preserving tissue architecture. However, analyzing spatial omics data is challenging due to the complexity of the outputs, including large-scale images, millions of transcripts, and numerous spatial coordinates. Moreover, standard volumetric segmentation is often hampered by optical blurring and signal bleed-through in out-of-focus z-planes, which built-in tools in current platforms (e.g. Xenium Explorer) cannot solve. To overcome these challenges, we introduce STAT3D, a transparent, time-efficient, and customizable pipeline for analyzing whole-tumor biopsy slides in a user-tailored manner, including a 3D cell segmentation approach focused on the images' sharpest z-layers. STAT3D addresses current limitations, such as generic image analysis and uniform downstream processing, by introducing an "image-tailored" strategy that selectively combines only the sharpest optical z-planes to calculate single-cell features and spatial distances. By integrating standard community tools (e.g. Seurat), the pipeline facilitates accurate multiplane cellular segmentation, tailored cell-to-transcript mapping, and fully automated singleR annotation. This versatile tool automatically streamlines critical steps in spatial omics analysis, which facilitates exploration of infiltrating cell types, interactions and tissue architectures by the scientific community.
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