Profiling of Single‐Cell Transcriptomes. Issue 3 (8th September 2017)

• Record Type: Journal Article
• Authors: Chen, Wanze; Gardeux, Vincent; Meireles‐Filho, Antonio; Deplancke, Bart
• Is Part Of: Current protocols in mouse biology. Volume 7:Issue 3(2017)
• Page Start: 145
• Page End: 175
• Publication Date: 2017-09-08
• Subjects: single‐cell -- transcriptomics -- scRNA‐seq -- Smart‐seq2 -- gene expression -- Tn5 -- tagmentation -- ASAP -- Web tool -- analysis pipeline; Mice -- Genetics -- Laboratory manuals; Mice; Animals, Laboratory; Research; Mice -- Genetics; Periodicals; Laboratory manuals; 616.027333
• DOI: 10.1002/cpmo.30
• Languages: English
• ISSNs: 2161-2617

Abstract

Abstract : Complex biological systems are composed of multiple cell types whose transcriptional activity can vary due to differences in cell state, environmental stimulation, or intrinsic programs. Conventional bulk analysis methods capture the average transcriptional programs of the cell population, thus missing the unique cellular signature of each single cell. In recent years, the development of single‐cell RNA‐sequencing (scRNA‐seq) technologies has provided a powerful approach to dissect the cellular heterogeneity of complex biological systems. However, such approaches require specialized equipment or are costly. In this article, we describe an improved Smart‐seq2‐based method to profile the transcriptome of hundreds of single cells simultaneously, without utilizing commercial kits or requiring any specialized single‐cell capture/library preparation tools. Moreover, we introduce the Automated Single‐cell Analysis Pipeline (ASAP), which allows researchers without strong computational expertise to explore scRNA‐seq data using a wide range of commonly used algorithms and sophisticated visualization tools. © 2017 by John Wiley & Sons, Inc.