CiteFuse enables multi-modal analysis of CITE-seq data

被引:65
作者
Kim, Hani Jieun [1 ,2 ,3 ]
Lin, Yingxin [1 ,2 ]
Geddes, Thomas A. [2 ,4 ]
Yang, Jean Yee Hwa [1 ,2 ]
Yang, Pengyi [1 ,2 ,3 ]
机构
[1] Univ Sydney, Fac Sci, Sch Math & Stat, Sydney, NSW 2006, Australia
[2] Univ Sydney, Charles Perkins Ctr, Sydney, NSW 2006, Australia
[3] Univ Sydney, Fac Med & Hlth, Childrens Med Res Inst, Computat Syst Biol Grp, Sydney, NSW 2145, Australia
[4] Univ Sydney, Fac Sci, Sch Life & Environm Sci, Sydney, NSW 2006, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
SINGLE; RECONSTRUCTION; HETEROGENEITY; EXPRESSION; PROTEINS;
D O I
10.1093/bioinformatics/btaa282
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Motivation: Multi-modal profiling of single cells represents one of the latest technological advancements in molecular biology. Among various single-cell multi-modal strategies, cellular indexing of transcriptomes and epitopes by sequencing (CITE-seq) allows simultaneous quantification of two distinct species: RNA and cell-surface proteins. Here, we introduce CiteFuse, a streamlined package consisting of a suite of tools for doublet detection, modality integration, clustering, differential RNA and protein expression analysis, antibody-derived tag evaluation, ligand-receptor interaction analysis and interactive web-based visualization of CITE-seq data. Results: We demonstrate the capacity of CiteFuse to integrate the two data modalities and its relative advantage against data generated from single-modality profiling using both simulations and real-world CITE-seq data. Furthermore, we illustrate a novel doublet detection method based on a combined index of cell hashing and transcriptome data. Finally, we demonstrate CiteFuse for predicting ligand-receptor interactions by using multi-modal CITE-seq data. Collectively, we demonstrate the utility and effectiveness of CiteFuse for the integrative analysis of transcriptome and epitope profiles from CITE-seq data.
引用
收藏
页码:4137 / 4143
页数:7
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