scRNA-seq data analysis method to improve analysis performance

被引:11
|
作者
Lu, Junru [1 ]
Sheng, Yuqi [1 ]
Qian, Weiheng [1 ]
Pan, Min [2 ]
Zhao, Xiangwei [1 ]
Ge, Qinyu [1 ]
机构
[1] Southeast Univ, Sch Biol Sci & Med Engn, State Key Lab Bioelect, Sipailou 2, Nanjing 210096, Peoples R China
[2] Southeast Univ, Sch Med, Nanjing, Peoples R China
基金
中国国家自然科学基金;
关键词
bioinformatics; biomedical engineering; genomics; RNA; CELL RNA-SEQ; GENE-EXPRESSION; SEQUENCING DATA; QUALITY-CONTROL; SINGLE; QUANTIFICATION; NORMALIZATION; TRANSCRIPTOME; CHALLENGES;
D O I
10.1049/nbt2.12115
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
With the development of single-cell RNA sequencing technology (scRNA-seq), we have the ability to study biological questions at the level of the individual cell transcriptome. Nowadays, many analysis tools, specifically suitable for single-cell RNA sequencing data, have been developed. In this review, the currently commonly used scRNA-seq protocols are discussed. The upstream processing flow pipeline of scRNA-seq data, including goals and popular tools for reads mapping and expression quantification, quality control, normalization, imputation, and batch effect removal is also introduced. Finally, methods to evaluate these tools in both cellular and genetic dimensions, clustering and differential expression analysis are presented.
引用
收藏
页码:246 / 256
页数:11
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