CORTEXA
← Browse
arxivcs.LGq-bio.GN2026-07-15

LATTICE: Graph Self-Supervised Learning for Multimodal Spatial Omics Integration

Jagan Mohan Reddy Dwarampudi, Veena Kochat, Suresh Satpati, Hien Van Nguyen, Kunal Rai, Tania Banerjee

Spatially resolved omics studies increasingly combine transcriptomic and epigenomic assays, yet downstream analysis is often still performed using single-modality pipelines. We present LATTICE (Latent Alignment of Tissue-level and Transcriptomic Information for Cross-modal Embedding), a graph-based self-supervised framework that learns spot-level representations from harmonized multimodal features. LATTICE integrates five aligned modality blocks per Visium spot: Visium RNA, scMultiome RNA, scMultiome ATAC, spatial ATAC, and spatial CUT\&Tag. These modalities capture spatial transcriptomic measurements, single-cell inferred regulatory activity, and in situ chromatin and histone states within a unified lattice representation. LATTICE constructs a spatial neighborhood graph and trains a TransformerConv encoder using masked reconstruction, cross-modal alignment, and spatial smoothness objectives. On a private 11-sample melanoma cohort from an anonymized clinical collaborator comprising 54{,}912 total spots, LATTICE demonstrated stable optimization behavior, reproducible embeddings across analysis seeds, and complete multimodal integration across all samples. Adding scMultiome RNA to Visium RNA alone substantially improved concordance with Space Ranger clusters across 11 runs (adjusted Rand index [ARI] +0.157, normalized mutual information [NMI] +0.143, and spatial contiguity +0.174). Additional modalities further improved spatial contiguity and multimodal utility score (MUS), although they sometimes reduced agreement with RNA-derived reference labels, likely because the learned embeddings captured chromatin and regulatory structure beyond transcriptomic similarity alone. These results position LATTICE as a practical and empirically grounded framework for multimodal spatial omics integration, while also highlighting the need for stronger supervision and broader external benchmarking.

View free PDFSource page

Related papers

arxivcs.LGq-bio.GN2026-06-26

scKDGM: KAN-guided Dynamic Graph Masked Learning for Single-Cell RNA-seq Clustering

Jun Tang, Pengwei Hu, Sicong Gao, Jie Guo, Lun Hu, Xin Luo

Single-cell RNA sequencing (scRNA-seq) clustering is essential for identifying cell types, but high dimensionality, sparsity, dropout, and technical noise hinder robust expression representation and cell graph construction. Existing masked autoencoders mainly use expression recov…

View free PDFSource page
arxivcs.LGq-bio.GN2026-07-23

HierarchicalDAEW: Domain-Aware Edge-Weighted Graph Convolution with Evidential Uncertainty for Multi-Section Spatial Gene Expression Prediction from H&E Histology

Kritanu Chattopadhyay, Soumya Chatterjee, Ondrej Krejcar, Debotosh Bhattacharjee

Spatial transcriptomics assays remain costly and technically demanding, restricting transcriptome-wide profiling to specialist settings and preventing routine clinical deployment. Predicting spatially resolved gene expression from H&E histology could close this gap, yet current m…

View free PDFSource page
arxivcs.LGq-bio.GN2026-07-06

Predictive single cell foundation model for gene regulation and aging with privacy-preserving tabular learning

Jiayuan Ding, Jianhui Lin, Ziyang Miao, Nils Mechtel, Shiyu Jiang, Yixin Wang, et al.

Pre-trained foundation models (FMs) have begun transforming single-cell genomics, but scaling them raises privacy concerns. Moreover, unlike text data, single-cell data is unordered and exhibits a unique tabular structure that current single-cell FMs overlook. We introduce Tabula…

View free PDFSource page
arxivstat.MLcs.LGq-bio.GN2026-07-05

Causal ASCEND: Scalable Two-tier Causal Discovery on High Dimensional Multi-omics Data

Stephen Asiedu, David Watson

Biological systems exhibit a hierarchical structure, characterised by directed flow from upstream regulators to downstream effects. Although this ordering provides a natural scaffold for causal inference, most causal discovery and GRN methods either ignore the tiered organisation…

View free PDFSource page
arxivq-bio.GNcs.LG2026-07-15

Screening of Biosecurity Features in Metagenomic Data with Evo 2 Probes

Jeremy Guntoro, Alexander Dack, Dylan Danno, Michaela Jančovičová, Križan Jurinović, Vanessa Smilansky

Genomic foundation models such as Evo 2 learn rich sequence representations, but their value for biosecurity screening is largely unexplored. We ask how much biosecurity-relevant signal is linearly accessible in these representations by training minimal linear and attention probe…

View free PDFSource page
arxivq-bio.GNcs.AIcs.LG2026-07-20

Making Single-Cell Data Distillation Auditable: Traceable Real-Cell Coresets via Discrete Min-Max Selection

Yaodi Luo, Peize He, Bowen Han, Lingbei Mengg

Single-cell datasets are increasingly costly to store, audit, and reuse for model training. Dimensionality reduction and dataset distillation can reduce this burden, but conventional distillation methods often produce synthetic expression profiles that cannot be traced to an assa…

View free PDFSource page