SORBET: Automated cell-neighborhood analysis of spatial transcriptomics or proteomics for interpretable sample classification via GNN
Shimonov, S.; Cunningham, J.; Talmon, R.; Aizenbud, L.; Desai, S.; Rimm, D.; Schalper, K.; Kluger, H.; Kluger, Y.
Show abstract
Spatial cellular profiling technologies have revolutionized our understanding of complex biological processes, from development and disease progression to immunity and aging. Despite their promise, integrating spatial information with multiplexed molecular data to accurately predict phenotypes poses significant challenges, especially in clinical settings. Here, we present SORBET, a geometric deep learning framework that directly analyzes complete spatial profiling data, eliminating the need to compress complete cell profiles into a limited set of annotations, such as cell types. SORBET models tissues as graphs of adjacent cells and applies graph convolutional networks to infer emergent phenotypes, such as responses to immunotherapy. The model leverages a novel data augmentation technique to ensure robust predictions, complemented by tailored interpretability analyses to identify the molecular and spatial patterns underlying the models phenotype inferences. We apply our method to a CosMx spatial transcriptomics dataset of pre-treatment metastatic melanoma samples annotated with response to immunotherapy; we show that spatial information significantly improves clinical endpoint, or phenotype, prediction and identifies important biological patterns. To our knowledge, SORBET is the first example of phenotype prediction on spatial transcriptomics data. We further validated our method using two spatial proteomics datasets, Imaging Mass Cytometry (IMC) and Co-detection by indexing (CODEX), obtained from Non-Small Cell Lung Cancer and Colorectal Cancer samples, respectively. SORBET demonstrates superior accuracy in phenotype prediction over leading spatial and non-spatial methods across various datasets of different observed phenotypes and technologies. SORBET sets a new benchmark for predictive analysis in spatial omics, promising to advance personalized medicine through refined patient treatment stratification, grounded in molecular and spatial tissue profiling.
Matching journals
The top 5 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Automated assignment of cell identity from single-cell multiplexed imaging and proteomic data 97%
- Uncovering the spatial landscape of molecular interactions within the tumor microenvironment through latent spaces 96%
- Belayer: Modeling discrete and continuous spatial variation in gene expression from spatially resolved transcriptomics 95%
Similar papers in this journal
- Randomized Spatial PCA (RASP): a computationally efficient method for dimensionality reduction of high-resolution spatial transcriptomics data 96%
- The Specious Art of Single-Cell Genomics 95%
- Highly Accurate Cancer Phenotype Prediction with AKLIMATE, a Stacked Kernel Learner Integrating Multimodal Genomic Data and Pathway Knowledge 95%
Similar papers in this journal
- Learning tissue representation by identification of persistent local patterns in spatial omics data 97%
- scMODAL: A general deep learning framework for comprehensive single-cell multi-omics data alignment with feature links 96%
- scDREAMER: atlas-level integration of single-cell datasets using deep generative model paired with adversarial classifier 96%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.