MMAP: A Multi-Magnification and Prototype-Aware Architecture for Predicting Spatial Gene Expression
Fuente:
arXiv
Enregistré dans:
| Auteurs principaux: | , , , , , |
|---|---|
| Format: | Preprint |
| Publié: |
2025
|
| Sujets: | |
| Accès en ligne: | |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
| _version_ | 1866914578745524224 |
|---|---|
| author | Nguyen, Hai Dang Pham, Nguyen Dang Huy Nguyen, The Minh Duc Nguyen, Dac Thai Nguyen, Hang Thi Nguyen, Duong M. |
| author_facet | Nguyen, Hai Dang Pham, Nguyen Dang Huy Nguyen, The Minh Duc Nguyen, Dac Thai Nguyen, Hang Thi Nguyen, Duong M. |
| contents | Spatial Transcriptomics (ST) enables the measurement of gene expression while preserving spatial information, offering critical insights into tissue architecture and disease pathology. Recent developments have explored the use of hematoxylin and eosin (H&E)-stained whole-slide images (WSIs) to predict transcriptome-wide gene expression profiles through deep neural networks. This task is commonly framed as a regression problem, where each input corresponds to a localized image patch extracted from the WSI. However, predicting spatial gene expression from histological images remains a challenging problem due to the significant modality gap between visual features and molecular signals. Recent studies have attempted to incorporate both local and global information into predictive models. Nevertheless, existing methods still suffer from two key limitations: (1) insufficient granularity in local feature extraction, and (2) inadequate coverage of global spatial context. In this work, we propose a novel framework, MMAP (Multi-MAgnification and Prototype-enhanced architecture), that addresses both challenges simultaneously. To enhance local feature granularity, MMAP leverages multi-magnification patch representations that capture fine-grained histological details. To improve global contextual understanding, it learns a set of latent prototype embeddings that serve as compact representations of slide-level information. Extensive experimental results demonstrate that MMAP consistently outperforms all existing state-of-the-art methods across multiple evaluation metrics, including Mean Absolute Error (MAE), Mean Squared Error (MSE), and Pearson Correlation Coefficient (PCC). |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2510_11344 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | MMAP: A Multi-Magnification and Prototype-Aware Architecture for Predicting Spatial Gene Expression Nguyen, Hai Dang Pham, Nguyen Dang Huy Nguyen, The Minh Duc Nguyen, Dac Thai Nguyen, Hang Thi Nguyen, Duong M. Computer Vision and Pattern Recognition Spatial Transcriptomics (ST) enables the measurement of gene expression while preserving spatial information, offering critical insights into tissue architecture and disease pathology. Recent developments have explored the use of hematoxylin and eosin (H&E)-stained whole-slide images (WSIs) to predict transcriptome-wide gene expression profiles through deep neural networks. This task is commonly framed as a regression problem, where each input corresponds to a localized image patch extracted from the WSI. However, predicting spatial gene expression from histological images remains a challenging problem due to the significant modality gap between visual features and molecular signals. Recent studies have attempted to incorporate both local and global information into predictive models. Nevertheless, existing methods still suffer from two key limitations: (1) insufficient granularity in local feature extraction, and (2) inadequate coverage of global spatial context. In this work, we propose a novel framework, MMAP (Multi-MAgnification and Prototype-enhanced architecture), that addresses both challenges simultaneously. To enhance local feature granularity, MMAP leverages multi-magnification patch representations that capture fine-grained histological details. To improve global contextual understanding, it learns a set of latent prototype embeddings that serve as compact representations of slide-level information. Extensive experimental results demonstrate that MMAP consistently outperforms all existing state-of-the-art methods across multiple evaluation metrics, including Mean Absolute Error (MAE), Mean Squared Error (MSE), and Pearson Correlation Coefficient (PCC). |
| title | MMAP: A Multi-Magnification and Prototype-Aware Architecture for Predicting Spatial Gene Expression |
| topic | Computer Vision and Pattern Recognition |
| url | https://arxiv.org/abs/2510.11344 |