The scINSIGHT Package for Integrating Single-Cell RNA-Seq Data from Different Biological Conditions

被引:0
作者
Qian, Kun [1 ]
Fu, Shiwei [2 ,3 ]
Li, Hongwei [1 ]
Li, Wei Vivian [2 ,3 ,4 ]
机构
[1] China Univ Geosci, Sch Math & Phys, Wuhan, Peoples R China
[2] Rutgers State Univ, Rutgers Sch Publ Hlth, Dept Biostat & Epidemiol, Piscataway, NJ USA
[3] Univ Calif Riverside, Dept Stat, Riverside, CA USA
[4] Univ Calif Riverside, Dept Stat, 900 Univ Ave,Olmsted Hall 1337, Riverside, CA 92591 USA
关键词
clustering; data integration; non-negative matrix factorization; scRNA-seq;
D O I
10.1089/cmb.2022.0244
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Data integration is a critical step in the analysis of multiple single-cell RNA sequencing samples to account for heterogeneity due to both biological and technical variability. scINSIGHT is a new integration method for single-cell gene expression data, and can effectively use the information of biological condition to improve the integration of multiple single-cell samples. scINSIGHT is based on a novel non-negative matrix factorization model that learns common and condition-specific gene modules in samples from different biological or experimental conditions. Using these gene modules, scINSIGHT can further identify cellular identities and active biological processes in different cell types or conditions. Here we introduce the installation and main functionality of the scINSIGHT R package, including how to preprocess the data, apply the scINSIGHT algorithm, and analyze the output.
引用
收藏
页码:1233 / 1236
页数:4
相关论文
共 8 条
[1]   A benchmark of batch-effect correction methods for single-cell RNA sequencing data [J].
Hoa Thi Nhu Tran ;
Ang, Kok Siong ;
Chevrier, Marion ;
Zhang, Xiaomeng ;
Lee, Nicole Yee Shin ;
Goh, Michelle ;
Chen, Jinmiao .
GENOME BIOLOGY, 2020, 21 (01)
[2]  
Qian K, 2022, GENOME BIOL, V23, DOI 10.1186/s13059-022-02649-3
[3]   Selecting gene features for unsupervised analysis of single-cell gene expression data [J].
Sheng, Jie ;
Li, Wei Vivian .
BRIEFINGS IN BIOINFORMATICS, 2021, 22 (06)
[4]   Decomposing Cell Identity for Transfer Learning across Cellular Measurements, Platforms, Tissues, and Species [J].
Stein-O'Brien, Genevieve L. ;
Clark, Brian S. ;
Sherman, Thomas ;
Zibetti, Cristina ;
Hu, Qiwen ;
Sealfon, Rachel ;
Liu, Sheng ;
Qian, Jiang ;
Colantuoni, Carlo ;
Blackshaw, Seth ;
Goff, Loyal A. ;
Fertig, Elana J. .
CELL SYSTEMS, 2019, 8 (05) :395-+
[5]   Comprehensive Integration of Single-Cell Data [J].
Stuart, Tim ;
Butler, Andrew ;
Hoffman, Paul ;
Hafemeister, Christoph ;
Papalexi, Efthymia ;
Mauck, William M., III ;
Hao, Yuhan ;
Stoeckius, Marlon ;
Smibert, Peter ;
Satija, Rahul .
CELL, 2019, 177 (07) :1888-+
[6]   Single-Cell Multi-omic Integration Compares and Contrasts Features of Brain Cell Identity [J].
Welch, Joshua D. ;
Kozareva, Velina ;
Ferreira, Ashley ;
Vanderburg, Charles ;
Martin, Carly ;
Macosko, Evan Z. .
CELL, 2019, 177 (07) :1873-+
[7]   A non-negative matrix factorization method for detecting modules in heterogeneous omics multi-modal data [J].
Yang, Zi ;
Michailidis, George .
BIOINFORMATICS, 2016, 32 (01) :1-8
[8]   Learning common and specific patterns from data of multiple interrelated biological scenarios with matrix factorization [J].
Zhang, Lihua ;
Zhang, Shihua .
NUCLEIC ACIDS RESEARCH, 2019, 47 (13) :6606-6617