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Global preamplification simplifies targeted mRNA quantification
The need to perform gene expression profiling using next generation sequencing and quantitative real-time PCR (qPCR) on small sample sizes and single cells is rapidly expanding. However, to analyse few molecules, preamplification is required. Here, we studied global and target-specific preamplificat...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362892/ https://www.ncbi.nlm.nih.gov/pubmed/28332609 http://dx.doi.org/10.1038/srep45219 |
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author | Kroneis, Thomas Jonasson, Emma Andersson, Daniel Dolatabadi, Soheila Ståhlberg, Anders |
author_facet | Kroneis, Thomas Jonasson, Emma Andersson, Daniel Dolatabadi, Soheila Ståhlberg, Anders |
author_sort | Kroneis, Thomas |
collection | PubMed |
description | The need to perform gene expression profiling using next generation sequencing and quantitative real-time PCR (qPCR) on small sample sizes and single cells is rapidly expanding. However, to analyse few molecules, preamplification is required. Here, we studied global and target-specific preamplification using 96 optimised qPCR assays. To evaluate the preamplification strategies, we monitored the reactions in real-time using SYBR Green I detection chemistry followed by melting curve analysis. Next, we compared yield and reproducibility of global preamplification to that of target-specific preamplification by qPCR using the same amount of total RNA. Global preamplification generated 9.3-fold lower yield and 1.6-fold lower reproducibility than target-specific preamplification. However, the performance of global preamplification is sufficient for most downstream applications and offers several advantages over target-specific preamplification. To demonstrate the potential of global preamplification we analysed the expression of 15 genes in 60 single cells. In conclusion, we show that global preamplification simplifies targeted gene expression profiling of small sample sizes by a flexible workflow. We outline the pros and cons for global preamplification compared to target-specific preamplification. |
format | Online Article Text |
id | pubmed-5362892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53628922017-03-24 Global preamplification simplifies targeted mRNA quantification Kroneis, Thomas Jonasson, Emma Andersson, Daniel Dolatabadi, Soheila Ståhlberg, Anders Sci Rep Article The need to perform gene expression profiling using next generation sequencing and quantitative real-time PCR (qPCR) on small sample sizes and single cells is rapidly expanding. However, to analyse few molecules, preamplification is required. Here, we studied global and target-specific preamplification using 96 optimised qPCR assays. To evaluate the preamplification strategies, we monitored the reactions in real-time using SYBR Green I detection chemistry followed by melting curve analysis. Next, we compared yield and reproducibility of global preamplification to that of target-specific preamplification by qPCR using the same amount of total RNA. Global preamplification generated 9.3-fold lower yield and 1.6-fold lower reproducibility than target-specific preamplification. However, the performance of global preamplification is sufficient for most downstream applications and offers several advantages over target-specific preamplification. To demonstrate the potential of global preamplification we analysed the expression of 15 genes in 60 single cells. In conclusion, we show that global preamplification simplifies targeted gene expression profiling of small sample sizes by a flexible workflow. We outline the pros and cons for global preamplification compared to target-specific preamplification. Nature Publishing Group 2017-03-23 /pmc/articles/PMC5362892/ /pubmed/28332609 http://dx.doi.org/10.1038/srep45219 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kroneis, Thomas Jonasson, Emma Andersson, Daniel Dolatabadi, Soheila Ståhlberg, Anders Global preamplification simplifies targeted mRNA quantification |
title | Global preamplification simplifies targeted mRNA quantification |
title_full | Global preamplification simplifies targeted mRNA quantification |
title_fullStr | Global preamplification simplifies targeted mRNA quantification |
title_full_unstemmed | Global preamplification simplifies targeted mRNA quantification |
title_short | Global preamplification simplifies targeted mRNA quantification |
title_sort | global preamplification simplifies targeted mrna quantification |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362892/ https://www.ncbi.nlm.nih.gov/pubmed/28332609 http://dx.doi.org/10.1038/srep45219 |
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