Metacells are disjoint and homogeneous groups of single-cell profiles, representing discrete and highly granular cell states. Existing metacell algorithms tend to use only one modality to infer metacells, even though single-cell multi-omics datasets profile multiple molecular modalities within the same cell. Here, we present \textbf{C}ross-M\textbf{O}dal \textbf{E}mbedding for \textbf{M}etaCell Identification (COEM), which utilizes an embedded space leveraging the information of both scATAC-seq and scRNA-seq to perform aggregation, balancing the trade-off between fine resolution and sufficient sequencing coverage. COEM outperforms the state-of-the-art method SEACells by efficiently identifying accurate and well-separated metacells across datasets with continuous and discrete cell types. Furthermore, COEM significantly improves peak-to-gene association analyses, and facilitates complex gene regulatory inference tasks.
@article{arxiv.2207.07734,
title = {COEM: Cross-Modal Embedding for MetaCell Identification},
author = {Haiyi Mao and Minxue Jia and Jason Xiaotian Dou and Haotian Zhang and Panayiotis V. Benos},
journal= {arXiv preprint arXiv:2207.07734},
year = {2022}
}
Comments
5 pages, 2 figures, ICML workshop on computational biology