Unsupervised topological alignment for single-cell multi-omics integration
Unsupervised topological alignment for single-cell multi-omics integration
复制标题
用于单细胞多组学集成的无监督拓扑比对
DOI:
10.1093/bioinformatics/btaa443
复制
发表时间:
2020-07-01
期刊:
影响因子:
5.8
通讯作者:
Wan, Lin
中科院分区:
文献类型:
--
作者:
Cao, Kai;Bai, Xiangqi;Wan, Lin
Single-cell multi-omics data provide a comprehensive molecular view of cells. However, single-cell multi-omics datasets consist of unpaired cells measured with distinct unmatched features across modalities, making data integration challenging. In this study, we present a novel algorithm, termed UnionCom, for the unsupervised topological alignment of single-cell multi-omics integration. UnionCom does not require any correspondence information, either among cells or among features. It first embeds the intrinsic low-dimensional structure of each single-cell dataset into a distance matrix of cells within the same dataset and then aligns the cells across single-cell multi-omics datasets by matching the distance matrices via a matrix optimization method. Finally, it projects the distinct unmatched features across single-cell datasets into a common embedding space for feature comparability of the aligned cells. To match the complex nonlinear geometrical distorted low-dimensional structures across datasets, UnionCom proposes and adjusts a global scaling parameter on distance matrices for aligning similar topological structures. It does not require one-to-one correspondence among cells across datasets, and it can accommodate samples with dataset-specific cell types. UnionCom outperforms state-of-the-art methods on both simulated and real single-cell multi-omics datasets. UnionCom is robust to parameter choices, as well as subsampling of features. UnionCom software is available at https://github.com/caokai1073/UnionCom.