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      Microarrays, deep sequencing and the true measure of the transcriptome

      review-article
      1 , , 1
      BMC Biology
      BioMed Central

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          Abstract

          Microarrays first made the analysis of the transcriptome possible, and have produced much important information. Today, however, researchers are increasingly turning to direct high-throughput sequencing - RNA-Seq - which has considerable advantages for examining transcriptome fine structure - for example in the detection of allele-specific expression and splice junctions. In this article, we discuss the relative merits of the two techniques, the inherent biases in each, and whether all of the vast body of array work needs to be revisited using the newer technology. We conclude that microarrays remain useful and accurate tools for measuring expression levels, and RNA-Seq complements and extends microarray measurements.

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          Author and article information

          Journal
          BMC Biol
          BMC Biology
          BioMed Central
          1741-7007
          2011
          31 May 2011
          : 9
          : 34
          Affiliations
          [1 ]Laboratory of Cellular and Developmental Biology, National Institute of Digestive, Diabetes, and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA
          Article
          1741-7007-9-34
          10.1186/1741-7007-9-34
          3104486
          21627854
          027a099a-1004-4ebd-8061-4a54e87b046c
          Copyright ©2011 Malone and Oliver; licensee BioMed Central Ltd.

          This is an open access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

          History
          : 12 October 2010
          : 31 May 2011
          Categories
          Review

          Life sciences
          Life sciences

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