The predictability of genes functionally relevant to disease is analysed and the effect of data transformation techniques, the use of predicted gene expression for detecting tissue domains, and the benefit of integrating histopathology foundation models are analysed.
Abstract
Abstract Motivation Spatial transcriptomics enables spatially-resolved measurement of gene expression in tissues, but its widespread adoption has been limited by high cost. Predicting gene expression profiles from histology images using deep learning has recently attracted broad interest as a promising and cost-effective spatial transcriptomics solution, yet the strengths and limitations of existing methods have not been comprehensively assessed. Results We reviewed current approaches and compared seven algorithms across six datasets spanning four cancer types and a non-cancer disease, covering three spatial protocols and a comprehensive set of performance measures. Unlike previous studies that focused only on highly variable genes, we also analysed the predictability of genes functionally relevant to disease. We further assessed out-of-domain performance, the effect of data transformation techniques, the use of predicted gene expression for detecting tissue domains, and the benefit of integrating histopathology foundation models. Our results provide new quantitative insights into the limitations and promise of deep learning based spatial transcriptomics methods, and suggest challenges and future directions. Availability and implementation The benchmarking pipeline and source code are available at https://github.com/BiomedicalMachineLearning/DeepHis2Exp.
Spatial transcriptomics (ST) maps gene expression within intact tissues, but its cost and technical complexity limit broad adoption. A growing body of deep-learning methods now seeks to infer ST directly from routine histology images, especially hematoxylin and eosin (H&E)-stained slides, with the aim of turning archiv...
Ke-Xin Xu, H. Koohy, A. Antanaviciute· EXO· 0 citations
Spatial transcriptomics (ST) enhances single-cell RNA sequencing by revealing transcript distribution, offering critical insights into heterogeneous diseases such as breast cancer. However, the high cost and lengthy processes of generating high-quality ST data limit clinical application. Recent deep learning methods pr...
MoSPR (Morpho-Spatial Program Regression), a linear framework that couples an adjacency-informed histology representation with a low-rank molecular basis, provides an interpretable link between spatially coherent macrostate regions and their associated molecular programs.
Dongmyung Shin, Geong-Ran Lee, Yesung Cho et al.· 0 citations
It is argued that the most credible translational goal is not to infer every transcript from H&E, but to identify biologically coherent spatial states with reproducible morphological correlates that can be validated across independent platforms and cohorts before being mapped across large archival collections.
Mohammad Amin Rezania, Haechan Yi, Jae-Il Choi et al.· Cancer research and treatmen...· 0 citations
CarHE (contrastive alignment of gene expression for hematoxylin and eosin images), a multimodal pretraining framework that infers high-dimensional spatial transcriptomic profiles from routine H&E-stained slides, provides a cost-effective and scalable framework for H&E-based spatial inference, supporting further validat...
Jiawei Zou, Kai Xiao, Ze-Xi Chen et al.· Cancer Research· 0 citations
Predicting spatial gene expression from histology images could scale spatial transcriptomics (ST) to image-only cohorts, but conventional histology-based ST prediction is trained and evaluated mainly by per-gene spatial-profile reconstruction. This objective is misaligned with a key downstream use of ST: differentially...
Kaito Shiku, Kazuya Nishimura, Yasuhiro Kojima et al.· 0 citations
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