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SpaDiT: Diffusion Transformer for Spatial Gene Expression Prediction using scRNA-seq

1 Pith paper cite this work, alongside 1 external citations. Polarity classification is still indexing.

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abstract

The rapid development of spatial transcriptomics (ST) technologies is revolutionizing our understanding of the spatial organization of biological tissues. Current ST methods, categorized into next-generation sequencing-based (seq-based) and fluorescence in situ hybridization-based (image-based) methods, offer innovative insights into the functional dynamics of biological tissues. However, these methods are limited by their cellular resolution and the quantity of genes they can detect. To address these limitations, we propose SpaDiT, a deep learning method that utilizes a diffusion generative model to integrate scRNA-seq and ST data for the prediction of undetected genes. By employing a Transformer-based diffusion model, SpaDiT not only accurately predicts unknown genes but also effectively generates the spatial structure of ST genes. We have demonstrated the effectiveness of SpaDiT through extensive experiments on both seq-based and image-based ST data. SpaDiT significantly contributes to ST gene prediction methods with its innovative approach. Compared to eight leading baseline methods, SpaDiT achieved state-of-the-art performance across multiple metrics, highlighting its substantial bioinformatics contribution.

fields

q-bio.QM 1

years

2025 1

verdicts

UNVERDICTED 1

representative citing papers

Emerging AI Approaches for Cancer Spatial Omics

q-bio.QM · 2025-06-30 · unverdicted · novelty 2.0

A review that groups AI methods for cancer spatial omics into data-driven, constraint-based, and mechanistic modeling paradigms, calling for more interpretable models and mouse-model-generated perturbational data.

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Showing 1 of 1 citing paper.

  • Emerging AI Approaches for Cancer Spatial Omics q-bio.QM · 2025-06-30 · unverdicted · none · ref 73 · internal anchor

    A review that groups AI methods for cancer spatial omics into data-driven, constraint-based, and mechanistic modeling paradigms, calling for more interpretable models and mouse-model-generated perturbational data.