Robust joint clustering of multi-omics single-cell data via multi-modal high-order neighborhood Laplacian matrix optimization

被引:1
作者
Jiang, Hao [1 ]
Zhan, Senwen [1 ]
Ching, Wai-Ki [2 ]
Chen, Luonan [3 ,4 ]
机构
[1] Renmin Univ China, Sch Math, Beijing 100872, Peoples R China
[2] Univ Hong Kong, Dept Math, Pokfulam Rd, Hong Kong, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Biochem & Cell Biol, CAS Ctr Excellence Mol Cell Sci, Key Lab Syst Biol, 320 YueYang Rd, Shanghai 200031, Peoples R China
[4] Chinese Acad Sci, Univ Chinese Acad Sci, Hangzhou Inst Adv Study, Sch Life Sci,Key Lab Syst Hlth Sci Zhejiang Prov, Hangzhou 310024, Peoples R China
基金
中国国家自然科学基金;
关键词
MESSENGER-RNA-SEQ;
D O I
10.1093/bioinformatics/btad414
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Simultaneous profiling of multi-omics single-cell data represents exciting technological advancements for understanding cellular states and heterogeneity. Cellular indexing of transcriptomes and epitopes by sequencing allowed for parallel quantification of cell-surface protein expression and transcriptome profiling in the same cells; methylome and transcriptome sequencing from single cells allows for analysis of transcriptomic and epigenomic profiling in the same individual cells. However, effective integration method for mining the heterogeneity of cells over the noisy, sparse, and complex multi-modal data is in growing need. Results: In this article, we propose a multi-modal high-order neighborhood Laplacian matrix optimization framework for integrating the multiomics single-cell data: scHoML. Hierarchical clustering method was presented for analyzing the optimal embedding representation and identifying cell clusters in a robust manner. This novel method by integrating high-order and multi-modal Laplacian matrices would robustly represent the complex data structures and allow for systematic analysis at the multi-omics single-cell level, thus promoting further biological discoveries.
引用
收藏
页数:13
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