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research article

Profiling of Single-Cell Transcriptomes

Chen, Wanze  
•
Gardeux, Vincent  
•
Meireles-Filho, Antonio  
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2017
Current Protocols in Mouse Biology

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 required specialized equipment or were costly. In this protocol, 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 a data analysis pipeline, named Automated Single-cell Analysis Pipeline (ASAP), that allows researchers without strong computational expertise to explore scRNA-seq data using a wide range of commonly used algorithms and sophisticated visualization tools.

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Type
research article
DOI
10.1002/cpmo.30
Author(s)
Chen, Wanze  
Gardeux, Vincent  
Meireles-Filho, Antonio  
Deplancke, Bart  
Date Issued

2017

Published in
Current Protocols in Mouse Biology
Volume

7

Issue

3

Start page

145

End page

175

Subjects

single-cell

•

transcriptomics

•

scRNA-seq

•

Smart-seq2

•

gene expression

•

Tn5

•

tagmentation

•

ASAP

•

web-tool

•

analysis pipeline

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
UPDEPLA  
FunderGrant Number

H2020

665667

EU funding

Marie Curie Intra European Fellowship within the 7th European Community Framework Programme

Swiss federal funding

31003A_162735

Available on Infoscience
April 25, 2020
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/168388
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