Proximogram-A multi-omics network-based framework to capture tissue heterogeneity integrating single-cell omics and spatial profiling.

Comput Biol Med

Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, USA; Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA; Department of Biostatistics, University of Michigan, Ann Arbor, MI, USA; Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA; Department of Radiation Oncology, University of Michigan, Ann Arbor, MI, USA. Electronic address:

Published: November 2024

AI Article Synopsis

  • The availability of diverse biological data is enabling more effective ways to analyze and combine this information for better disease understanding.
  • The authors introduce "Proximogram," a graph-based model that integrates various biological datasets, specifically using multiplexed immunofluorescence and single-cell RNA-seq data from pancreatic disease patients.
  • The study demonstrates that using proximograms in graph deep-learning models leads to better classification results by merging structural data from cell interactions with spatial cell layouts, highlighting potential diagnostic markers.

Article Abstract

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.

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Source
http://dx.doi.org/10.1016/j.compbiomed.2024.109082DOI Listing

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