GNLGSep 19, 2024

PRAGA: Prototype-aware Graph Adaptive Aggregation for Spatial Multi-modal Omics Analysis

arXiv:2409.12728v526 citationsh-index: 4Has Code
Originality Incremental advance
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This addresses a domain-specific problem in computational biology for researchers analyzing spatial multi-modal omics data, offering an incremental improvement over existing graph-based methods.

The paper tackles the problem of spatial multi-modal omics analysis, where fixed KNN graphs fail to capture latent semantic relations due to data perturbations and lack of annotation priors, by proposing PRAGA, a framework that constructs dynamic graphs and uses prototype contrastive learning, achieving superior performance over 7 competing methods on simulated and real datasets.

Spatial multi-modal omics technology, highlighted by Nature Methods as an advanced biological technique in 2023, plays a critical role in resolving biological regulatory processes with spatial context. Recently, graph neural networks based on K-nearest neighbor (KNN) graphs have gained prominence in spatial multi-modal omics methods due to their ability to model semantic relations between sequencing spots. However, the fixed KNN graph fails to capture the latent semantic relations hidden by the inevitable data perturbations during the biological sequencing process, resulting in the loss of semantic information. In addition, the common lack of spot annotation and class number priors in practice further hinders the optimization of spatial multi-modal omics models. Here, we propose a novel spatial multi-modal omics resolved framework, termed PRototype-Aware Graph Adaptative Aggregation for Spatial Multi-modal Omics Analysis (PRAGA). PRAGA constructs a dynamic graph to capture latent semantic relations and comprehensively integrate spatial information and feature semantics. The learnable graph structure can also denoise perturbations by learning cross-modal knowledge. Moreover, a dynamic prototype contrastive learning is proposed based on the dynamic adaptability of Bayesian Gaussian Mixture Models to optimize the multi-modal omics representations for unknown biological priors. Quantitative and qualitative experiments on simulated and real datasets with 7 competing methods demonstrate the superior performance of PRAGA. Code is available at https://github.com/Xubin-s-Lab/PRAGA.

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