Summary
In multi-cellular organisms, cell identity and functions are primed and refined through interactions with other surrounding cells. Here, we propose a scalable machine learning method, termed SPRUCE, which is designed to systematically ascertain common cell-cell communication patterns embedded in single-cell RNA-seq data. We applied our approach to investigate tumour microenvironments consolidating multiple breast cancer data sets and found seven frequently-observed interaction signatures and underlying gene-gene interaction networks. Our results implicate that a part of tumour heterogeneity, especially within the same subtype, is better understood by differential interaction patterns rather than the static expression of known marker genes.
Competing Interest Statement
The authors have declared no competing interest.
Footnotes
Lead contact: Yongjin P. Park, ypp{at}stat.ubc.ca, yongjin.park{at}ubc.ca
Revised to address the reviewers.