A sensitive and integrated approach to profile messenger RNA from samples with low cell numbers
A sensitive and integrated approach to profile messenger RNA from samples with low cell numbers
Transcriptomic profiling by RNA sequencing (RNA-Seq) represents the preferred approach to measure genome-wide gene expression for understanding cellular function, tissue development, disease pathogenesis, as well as to identify potential biomarkers and therapeutic targets. For samples with small cell numbers, multiple methods have been described to increase the efficiency of library preparation and to reduce hands-on time and costs. This chapter reviews our approach, which combines flow cytometry and the most recent high-resolution techniques to perform RNA-Seq for samples with low cell numbers as well as for single-cell samples. Our approach reduces technical variability while increasing sensitivity and efficiency. Thus, it is well-suited for large-scale gene expression profiling studies with limited samples for basic and clinical studies.
Journal Article
275-301
Rosales, Sandy Lisette
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Liang, Shu
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Engel, Isaac
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Schmiedel, Benjamin Joachim
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Kronenberg, Mitchell
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Vijayanand, Pandurangan
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Seumois, Grégory
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2018
Rosales, Sandy Lisette
04c96f2d-c7af-44e8-83dd-29568d77d40c
Liang, Shu
ef10b70c-61f7-4c74-89bf-11870742a9c5
Engel, Isaac
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Schmiedel, Benjamin Joachim
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Kronenberg, Mitchell
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Vijayanand, Pandurangan
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Seumois, Grégory
0be7d3d6-5526-458c-aa5c-cce52410a2ed
Rosales, Sandy Lisette, Liang, Shu, Engel, Isaac, Schmiedel, Benjamin Joachim, Kronenberg, Mitchell, Vijayanand, Pandurangan and Seumois, Grégory
(2018)
A sensitive and integrated approach to profile messenger RNA from samples with low cell numbers.
In,
Reinhardt, R.
(ed.)
Type 2 Immunity.
(Methods in Molecular Biology, 1799)
New York, NY.
Humana Press, .
(doi:10.1007/978-1-4939-7896-0_21).
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Book Section
Abstract
Transcriptomic profiling by RNA sequencing (RNA-Seq) represents the preferred approach to measure genome-wide gene expression for understanding cellular function, tissue development, disease pathogenesis, as well as to identify potential biomarkers and therapeutic targets. For samples with small cell numbers, multiple methods have been described to increase the efficiency of library preparation and to reduce hands-on time and costs. This chapter reviews our approach, which combines flow cytometry and the most recent high-resolution techniques to perform RNA-Seq for samples with low cell numbers as well as for single-cell samples. Our approach reduces technical variability while increasing sensitivity and efficiency. Thus, it is well-suited for large-scale gene expression profiling studies with limited samples for basic and clinical studies.
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e-pub ahead of print date: 29 June 2018
Published date: 2018
Keywords:
Journal Article
Identifiers
Local EPrints ID: 424693
URI: http://eprints.soton.ac.uk/id/eprint/424693
ISSN: 1064-3745
PURE UUID: d7901ab2-88fa-4ea1-8efb-b3d758da6f93
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Date deposited: 05 Oct 2018 11:40
Last modified: 16 Mar 2024 07:00
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Contributors
Author:
Sandy Lisette Rosales
Author:
Shu Liang
Author:
Isaac Engel
Author:
Benjamin Joachim Schmiedel
Author:
Mitchell Kronenberg
Author:
Pandurangan Vijayanand
Author:
Grégory Seumois
Editor:
R. Reinhardt
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