Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
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
_version_ 1782384197798723584
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
work_keys_str_mv AT collinsjohne highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping
AT walineha highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping
AT sealyianm highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping
AT morrisjamesa highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping
AT whiterichardj highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping
AT leonardstevenr highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping
AT jacksondavidk highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping
AT jonesmatthewc highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping
AT smerdonnathaliec highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping
AT zamorajorge highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping
AT dooleychristopherm highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping
AT carrutherssamanthan highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping
AT barrettjeffreyc highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping
AT stemplederekl highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping
AT buschnentwichelisabethm highthroughputandquantitativegenomewidemessengerrnasequencingformolecularphenotyping