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Studying bacterial transcriptomes using RNA-seq

Genome-wide studies of bacterial gene expression are shifting from microarray technology to second generation sequencing platforms. RNA-seq has a number of advantages over hybridization-based techniques, such as annotation-independent detection of transcription, improved sensitivity and increased dy...

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Detalles Bibliográficos
Autores principales: Croucher, Nicholas J, Thomson, Nicholas R
Formato: Texto
Lenguaje:English
Publicado: Current Biology 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025319/
https://www.ncbi.nlm.nih.gov/pubmed/20888288
http://dx.doi.org/10.1016/j.mib.2010.09.009
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author Croucher, Nicholas J
Thomson, Nicholas R
author_facet Croucher, Nicholas J
Thomson, Nicholas R
author_sort Croucher, Nicholas J
collection PubMed
description Genome-wide studies of bacterial gene expression are shifting from microarray technology to second generation sequencing platforms. RNA-seq has a number of advantages over hybridization-based techniques, such as annotation-independent detection of transcription, improved sensitivity and increased dynamic range. Early studies have uncovered a wealth of novel coding sequences and non-coding RNA, and are revealing a transcriptional landscape that increasingly mirrors that of eukaryotes. Already basic RNA-seq protocols have been improved and adapted to looking at particular aspects of RNA biology, often with an emphasis on non-coding RNAs, and further refinements to current techniques will improve our understanding of gene expression, and genome content, in the future.
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spelling pubmed-30253192011-02-10 Studying bacterial transcriptomes using RNA-seq Croucher, Nicholas J Thomson, Nicholas R Curr Opin Microbiol Article Genome-wide studies of bacterial gene expression are shifting from microarray technology to second generation sequencing platforms. RNA-seq has a number of advantages over hybridization-based techniques, such as annotation-independent detection of transcription, improved sensitivity and increased dynamic range. Early studies have uncovered a wealth of novel coding sequences and non-coding RNA, and are revealing a transcriptional landscape that increasingly mirrors that of eukaryotes. Already basic RNA-seq protocols have been improved and adapted to looking at particular aspects of RNA biology, often with an emphasis on non-coding RNAs, and further refinements to current techniques will improve our understanding of gene expression, and genome content, in the future. Current Biology 2010-10 /pmc/articles/PMC3025319/ /pubmed/20888288 http://dx.doi.org/10.1016/j.mib.2010.09.009 Text en © 2010 Elsevier Ltd. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Croucher, Nicholas J
Thomson, Nicholas R
Studying bacterial transcriptomes using RNA-seq
title Studying bacterial transcriptomes using RNA-seq
title_full Studying bacterial transcriptomes using RNA-seq
title_fullStr Studying bacterial transcriptomes using RNA-seq
title_full_unstemmed Studying bacterial transcriptomes using RNA-seq
title_short Studying bacterial transcriptomes using RNA-seq
title_sort studying bacterial transcriptomes using rna-seq
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025319/
https://www.ncbi.nlm.nih.gov/pubmed/20888288
http://dx.doi.org/10.1016/j.mib.2010.09.009
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