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Massive and parallel expression profiling using microarrayed single-cell sequencing

delete2016-10-14
delete45
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OA
AI
S
Sanja Vicković
P
Patrik L. Ståhl
F
Fredrik Salmén
S
Sarantis Giatrellis
J
Jakub Orzechowski Westholm
A
Annelie Mollbrink
J
José Fernández Navarro
J
Joaquín Custodio
M
Magda Bienko
L
Lesley‐Ann Sutton
R
Richard Rosenquist
J
Jonas Frisén
J
Joakim Lundeberg *
DOI:10.1038/ncomms13182delete
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Abstract

Abstract

En 中文
Single-cell transcriptome analysis overcomes problems inherently associated with averaging gene expression measurements in bulk analysis. However, single-cell analysis is currently challenging in terms of cost, throughput and robustness. Here, we present a method enabling massive microarray-based barcoding of expression patterns in single cells, termed MASC-seq. This technology enables both imaging and high-throughput single-cell analysis, characterizing thousands of single-cell transcriptomes per day at a low cost (0.13 USD/cell), which is two orders of magnitude less than commercially available systems. Our novel approach provides data in a rapid and simple way. Therefore, MASC-seq has the potential to accelerate the study of subtle clonal dynamics and help provide critical insights into disease development and other biological processes.
Keywords:
ACUTE MYELOID-LEUKEMIA
GENE-EXPRESSION
RNA-SEQ
IDENTIFICATION
HETEROGENEITY
PROGRESSION
CYCLE
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Journal

Nature Communications cover
Nature Communications
IF:
15.7
Papers:
9.2W
Citations:
91.2W

Organization

R
Royal Institute of Technology
Scholars:
1.8W
Papers: 1.8W
Citations: 25
S
Stockholm University
Scholars:
1.8W
Papers: 1.7W
Citations: 32
U
uppsala university
Scholars:
3.7W
Papers: 3.4W
Citations: 47
K
Karolinska Institutet
Scholars:
5.8W
Papers: 4.8W
Citations: 7.1W
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