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Sarigun, A.

Publications and source records attributed to Sarigun, A..

2 recordsLinked to original sources

SpaCEy: Discovery of Functional Spatial Tissue Patterns by Association with Clinical Features Using Explainable Graph Neural Networks

Tissues are complex ecosystems tightly organized in space. This organization influences their function, and its alteration underpins multiple diseases. Spatial omics allows us to profile its molecular basis, but how to leverage these data to link spatial organization and molecular patterns to clinical practice remains a challenge. We present SpaCEy (Spatial Clinical Explainability), an explainable graph neural network that uncovers organizational tissue patterns predictive of clinical outcomes. SpaCEy learns directly from molecular marker expression by modelling tissues as spatial graphs of cells and their interactions, without requiring predefined cell types or anatomical regions. Its embeddings capture intercellular relationships and molecular dependencies that enable accurate prediction of variables such as overall survival and disease progression. SpaCEy integrates a specialized explainer module that reveals recurring spatial patterns of cell organisation and coordinated marker expression that are most relevant to predictions of the models. Applied to a spatially resolved proteomic lung cancer cohort, SpaCEy discovers distinct spatial arrangements of cells together with coordinated expression of protein markers associated with disease progression. Across multiple breast cancer proteomic datasets, it consistently stratifies patients according to overall survival, both across and within established clinical subtypes. SpaCEy also highlights spatial patterns of a small set of key protein markers underlying this patient stratification.

bioinformatics↗

Flexynesis: A deep learning framework for bulk multi-omics data integration for precision oncology and beyond

Accurate decision making in precision oncology depends on integration of multimodal molecular information, such as the genetic data, gene expression, protein abundance, and epigenetic measurements. Deep learning methods facilitate integration of heterogeneous datasets. However, almost all published deep learning-based bulk multi-omics integration methods have constrained usability. They suffer from lack of transparency, modularity, deployability, and are applicable exclusively to narrow tasks. To address these limitations, we introduce Flexynesis, a versatile tool designed with usability, and adaptability in mind. Flexynesis streamlines data processing, enforces structured data splitting, and ensures rigorous model evaluation. It offers unsupervised feature selection, different omics layer fusion options, and hyperparameter tuning. Users can choose from distinct architectures - fully connected networks, variational autoencoders, multi-triplet networks, graph neural networks, and cross-modality encoding networks. Each model is complemented with a straightforward input interface and standardized training, evaluation, and feature importance quantification methods, enabling easy incorporation into data integration pipelines. For improved user experience, Flexynesis supports features such as on-the-fly task determination and compatibility with regression, classification, and survival modeling. It accommodates multi-task prediction of a mixture of numerical/categorical outcome variables with a tolerance for missing labels. We also developed an extensive benchmarking pipeline, showcasing the tools capability across diverse real-life datasets. This toolset should make deep-learning based bulk multi-omics data integration in the context of clinical/pre-clinical data analysis and marker discovery more accessible to a wider audience with or without experience in deep-learning development. Flexynesis is available at https://github.com/BIMSBbioinfo/flexynesis and can be installed from https://pypi.org/project/flexynesis/. O_FIG O_LINKSMALLFIG WIDTH=199 HEIGHT=200 SRC="FIGDIR/small/603606v1_ufig1.gif" ALT="Figure 1"> View larger version (53K): org.highwire.dtl.DTLVardef@17eda85org.highwire.dtl.DTLVardef@13c89ecorg.highwire.dtl.DTLVardef@182f706org.highwire.dtl.DTLVardef@127d9d9_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOGraphical Abstract:C_FLOATNO Summary of the Flexynesis data integration and analysis workflow. C_FIG

bioinformatics↗