The authors report a transfer learning framework designed to integrate scRNA-seq data across species by combining RNA expression with embeddings from protein language models and general-purpose language models, establishing Unify as a powerful method for comparative single-cell genomics and evolutionary biology.
Abstract
Integrating single-cell RNA-sequencing (scRNA-seq) data across species is hindered by evolutionary divergence, technical batch effects, and the reliance on one-to-one orthologs. Here, we present Unify, a transfer learning methodology that learns universal cell embeddings by defining functionally coherent, multi-modal macrogenes. This is achieved by combining RNA expression with embeddings from protein language models and general-purpose language models. Unify transcends species boundaries, enabling cross-species comparisons beyond strict gene-level homology. Unify corrects batch effects while preserving conserved biological signals across vast evolutionary distances and enables more accurate prediction of perturbation responses across species, such as from mouse to human. Applied to species separated by over 700 million years, Unify reconstructs more accurate multi-species cell-type evolutionary trees and uncovers convergent gene programs. Together, these results establish Unify as a powerful method for comparative single-cell genomics and evolutionary biology. Integrating single-cell RNA-sequencing (scRNA-seq) data across species is still technically challenging. Here, the authors report a transfer learning framework designed to integrate scRNA-seq data across species by combining RNA expression with embeddings from protein language models and general-purpose language models.
LucaCell, a sequence-centric foundation model that represents genes through pre-trained mRNA sequence embeddings rather than static gene annotations, is presented, showing that sequence-informed gene representation can improve the generalization of single-cell foundation models across species, data types, and predictiv...
Yan Sun, Yong He, Min-Si Ren et al.· bioRxiv· 0 citations
Abstract Single-cell RNA sequencing provides an unprecedented resolution for cellular heterogeneity and gene regulation, fostering cross-species comparative analyses with increasing interspecies data. However, integrating single-cell transcriptomic data faces challenges, including gene selection, evolutionary distance,...
Ruo-Lin Wang, Jun-Juan Zheng, C. Mao et al.· Briefings in Bioinformatics· 0 citations
CycloCross is introduced, an adversarial method based on the CycleGAN architecture, designed to translate scRNA-seq data between species without requiring a priori gene correspondences, and generates biologically plausible samples even with limited data, outperforming traditional generative models.
Deciphering the regulatory consequences of sequence divergence across human evolution is essential to understanding the molecular basis of human-specific traits and disease. Although millions of derived alleles distinguish humans from great apes, only a small fraction are likely to influence human-specific traits. Prev...
Riley J. Mangan, Nikitha Thoduguli, Dimitar Ivanov et al.· bioRxiv· 0 citations
This work introduces ensemble refinement for scRNA-seq and scATAC-seq embeddings, inspired by ensemble methods from statistical machine learning, and implements BatchRefiner, a fast post-processing tool to enhance batch integration.
Daniel E. Schäffer, Helen Kang, E. D. Aksu et al.· bioRxiv· 0 citations
GPN-Star substantially outperforms previous methods in prioritizing pathogenic and fine-mapped genome-wide association study variants, yields strong enrichments of complex trait heritability and improves power in rare variant association testing, which positions GPN-Star as a scalable, powerful and flexible tool for ge...
Cheng-Zhong Ye, Gonzalo Benegas, Carlos Albors et al.· Nature· 7 citations· ⚡1
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