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High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping
BACKGROUND: We present a genome-wide messenger RNA (mRNA) sequencing technique that converts small amounts of RNA from many samples into molecular phenotypes. It encompasses all steps from sample preparation to sequence analysis and is applicable to baseline profiling or perturbation measurements. R...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4524448/ https://www.ncbi.nlm.nih.gov/pubmed/26238335 http://dx.doi.org/10.1186/s12864-015-1788-6 |
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author | Collins, John E. Wali, Neha Sealy, Ian M. Morris, James A. White, Richard J. Leonard, Steven R. Jackson, David K. Jones, Matthew C. Smerdon, Nathalie C. Zamora, Jorge Dooley, Christopher M. Carruthers, Samantha N. Barrett, Jeffrey C. Stemple, Derek L. Busch-Nentwich, Elisabeth M. |
author_facet | Collins, John E. Wali, Neha Sealy, Ian M. Morris, James A. White, Richard J. Leonard, Steven R. Jackson, David K. Jones, Matthew C. Smerdon, Nathalie C. Zamora, Jorge Dooley, Christopher M. Carruthers, Samantha N. Barrett, Jeffrey C. Stemple, Derek L. Busch-Nentwich, Elisabeth M. |
author_sort | Collins, John E. |
collection | PubMed |
description | BACKGROUND: We present a genome-wide messenger RNA (mRNA) sequencing technique that converts small amounts of RNA from many samples into molecular phenotypes. It encompasses all steps from sample preparation to sequence analysis and is applicable to baseline profiling or perturbation measurements. RESULTS: Multiplex sequencing of transcript 3′ ends identifies differential transcript abundance independent of gene annotation. We show that increasing biological replicate number while maintaining the total amount of sequencing identifies more differentially abundant transcripts. CONCLUSIONS: This method can be implemented on polyadenylated RNA from any organism with an annotated reference genome and in any laboratory with access to Illumina sequencing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1788-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4524448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45244482015-08-05 High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping Collins, John E. Wali, Neha Sealy, Ian M. Morris, James A. White, Richard J. Leonard, Steven R. Jackson, David K. Jones, Matthew C. Smerdon, Nathalie C. Zamora, Jorge Dooley, Christopher M. Carruthers, Samantha N. Barrett, Jeffrey C. Stemple, Derek L. Busch-Nentwich, Elisabeth M. BMC Genomics Methodology Article BACKGROUND: We present a genome-wide messenger RNA (mRNA) sequencing technique that converts small amounts of RNA from many samples into molecular phenotypes. It encompasses all steps from sample preparation to sequence analysis and is applicable to baseline profiling or perturbation measurements. RESULTS: Multiplex sequencing of transcript 3′ ends identifies differential transcript abundance independent of gene annotation. We show that increasing biological replicate number while maintaining the total amount of sequencing identifies more differentially abundant transcripts. CONCLUSIONS: This method can be implemented on polyadenylated RNA from any organism with an annotated reference genome and in any laboratory with access to Illumina sequencing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1788-6) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-05 /pmc/articles/PMC4524448/ /pubmed/26238335 http://dx.doi.org/10.1186/s12864-015-1788-6 Text en © Collins et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Article Collins, John E. Wali, Neha Sealy, Ian M. Morris, James A. White, Richard J. Leonard, Steven R. Jackson, David K. Jones, Matthew C. Smerdon, Nathalie C. Zamora, Jorge Dooley, Christopher M. Carruthers, Samantha N. Barrett, Jeffrey C. Stemple, Derek L. Busch-Nentwich, Elisabeth M. High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping |
title | High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping |
title_full | High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping |
title_fullStr | High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping |
title_full_unstemmed | High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping |
title_short | High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping |
title_sort | high-throughput and quantitative genome-wide messenger rna sequencing for molecular phenotyping |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4524448/ https://www.ncbi.nlm.nih.gov/pubmed/26238335 http://dx.doi.org/10.1186/s12864-015-1788-6 |
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