Cross-species integration of single-cell data reveals conserved pathology-associated cell populations across animal
Cancheng Li1, Hongtao Sang1, Dayong Yue1
1The Fourth Affiliated Hospital of Soochow University, Biomedical Basic Research Center of Jiangsu, Institutes of Biology and Medical Sciences, Soochow University, Suzhou, Jiangsu 215123, China; Jiangsu Key Laboratory of Infection and Immunity, Soochow University, Suzhou, Jiangsu 215123, China.
Abstract:
Single-cell RNA sequencing (scRNA-seq) enables high-resolution profiling of cellular heterogeneity, but integrating data across species remains challenging due to technical variation and complex gene homology. We present TACMAN (transformer-based alignment of cross-species metapath aggregation network), a computational framework for cross-species scRNA-seq integration that combines a metapath-based heterogeneous graph neural network with an encoder-only transformer. TACMAN aligns conserved cell types across species under normal physiological conditions while preserving biological signals. We demonstrate its utility by integrating clinical human and mammalian model scRNA-seq data, revealing conserved cell subtypes in tumor, inflammatory, and infectious diseases. Notably, using our in-house single-cell transcriptomic atlas of an evolutionarily distant Caenorhabditis elegans germline tumor model, TACMAN identifies tumor-related cell populations conserved in human testicular germ cell tumor samples, enabling cross-species comparison under pathological conditions. TACMAN thus offers a powerful tool for comparative single-cell analysis, advancing translational research using animal models.


