Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, USA.
Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA.
Comput Biol Med. 2024 Nov;182:109082. doi: 10.1016/j.compbiomed.2024.109082. Epub 2024 Sep 9.
The increasing availability of patient-derived multimodal biological data for various diseases has opened up avenues for finding the optimal methods for jointly leveraging the information extracted in a customizable and scalable manner. Here, we propose the Proximogram, a graph-based representation that provides a joint construct for embedding independently obtained omics and spatial data. To evaluate the representation, we generated proximograms from 2 distinct biological sources, namely, multiplexed immunofluorescence images and single-cell RNA-seq data obtained from patients across two pancreatic diseases that include normal and chronic Pancreatitis (CP) and pancreatic ductal adenocarcinoma (PDAC). The generated proximograms were used as inputs to 2 distinct graph deep-learning models. The improved classification results over simpler spatial-data-based input graphs point to the increased discriminatory power obtained by integrating structural information from single-cell ligand-receptor signaling data and the spatial architecture of cells in each disease class, which can help point to markers of high diagnostic significance.
越来越多的各种疾病的患者衍生的多模态生物数据的出现,为以可定制和可扩展的方式联合利用提取信息的最佳方法开辟了道路。在这里,我们提出了 Proximogram,这是一种基于图的表示,它为嵌入独立获得的组学和空间数据提供了一个联合结构。为了评估表示,我们从两个不同的生物学来源生成了 Proximogram,即来自两个胰腺疾病(包括正常和慢性胰腺炎(CP)和胰腺导管腺癌(PDAC))的患者的多重免疫荧光图像和单细胞 RNA-seq 数据。生成的 Proximogram 用作两个不同图深度学习模型的输入。与基于更简单空间数据的输入图相比,分类结果的改善表明,通过整合来自单细胞配体-受体信号数据的结构信息和每个疾病类别的细胞的空间结构,获得了更高的辨别力,这有助于指出具有高诊断意义的标志物。