Single-cell Transcriptome Study as Big Data

被引:23
作者
Yu, Pingjian [1 ]
Lin, Wei [1 ]
机构
[1] Baylor Inst Immunol Res, Genom & Bioinformat Lab, Dallas, TX 75204 USA
关键词
DIFFERENTIAL EXPRESSION ANALYSIS; GENOME-WIDE ASSOCIATION; RNA-SEQ ANALYSIS; GENE-EXPRESSION; SEQUENCING DATA; HADOOP; NORMALIZATION; FRAMEWORK; MAPREDUCE; TOOL;
D O I
10.1016/j.gpb.2016.01.005
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The rapid growth of single-cell RNA-seq studies (scRNA-seq) demands efficient data storage, processing, and analysis. Big-data technology provides a framework that facilitates the comprehensive discovery of biological signals from inter-institutional scRNA-seq datasets. The strategies to solve the stochastic and heterogeneous single-cell transcriptome signal are discussed in this article. After extensively reviewing the available big-data applications of next-generation sequencing (NGS)-based studies, we propose a workflow that accounts for the unique characteristics of scRNA-seq data and primary objectives of single-cell studies.
引用
收藏
页码:21 / 30
页数:10
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