The rapid development of single-cell joint profiling technologies enables the simultaneous measurement of multiple molecular modalities from the same cell, providing unprecedented opportunities to characterize cellular heterogeneity. However, effectively integrating heterogeneous and high-dimensional multi-omics data remains a fundamental challenge for accurate cell clustering. In this work, we propose scCLC, a topology-aware contrastive learning framework for clustering single-cell multi-omics data. scCLC adopts contrastive learning as the backbone for cell representation learning and introduces a dedicated multi-view data augmentation strategy to address modality-specific characteristics. By exploiting the intrinsic cell-cell topological structures constructed from multi-omics data, scCLC identifies informative positive pairs for self-supervised training, which encourages the learned representations to be more cluster-discriminative. Extensive experiments on multiple paired datasets demonstrate the effectiveness of scCLC for clustering single-cell multi-omics data. Visualization analyses further indicate that scCLC is capable of distinguishing rare cell populations in highly imbalanced datasets. Moreover, case studies on single-cell triple-omics datasets illustrate that scCLC can be readily extended to integrate additional modalities, underscoring its flexibility and scalability for multi-omics data analysis. The source code can be downloaded from https://github.com/CSUBioGroup/scCLC.
Zhenlan Liang, Ruiqing Zheng, Huayu Tao et al.· IEEE transactions on computa...· 0 citations
Abstract Motivation Spatial transcriptomics (ST) enables molecular profiling within native tissue architecture, yet accurate delineation of spatial domains in ST data is challenging, as it demands the coordinated integration of transcriptomic, spatial, and tissue histological information. Results We present SRLST, an unsupervised representation learning framework that holistically harmonize these three complementary data modalities to precisely uncover tissue organization. SRLST employs a dual-graph variational autoencoding strategy to jointly model spatial proximity and morphological relations, fusing these with gene-expression embeddings into a unified latent space. Across distinct experimental datasets, SRLST consistently outperforms existing methods in delineating cortical organization, identifying small discontinuous tissue compartments, and capturing complex intratumor heterogeneity. Availability and implementation The code implementation of the SRLST algorithm is available at https://github.com/lanbiolab/SRLST.