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Transcriptome Sequencing: RNA-Seq

  • Hong Zhang
  • Lin He
  • Lei Cai
Part of the Methods in Molecular Biology book series (MIMB, volume 1754)

Abstract

RNA sequencing (RNA-seq) can not only be used to identify the expression of common or rare transcripts but also in the identification of other abnormal events, such as alternative splicing, novel transcripts, and fusion genes. In principle, RNA-seq can be carried out by almost all of the next-generation sequencing (NGS) platforms, but the libraries of different platforms are not exactly the same; each platform has its own kit to meet the special requirements of the instrument design.

Key words

Next-generation sequencing RNA sequencing Messenger RNA Library construction Data analysis 

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  • Hong Zhang
    • 1
  • Lin He
    • 1
  • Lei Cai
    • 1
  1. 1.Bio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Collaborative Innovation Center for Genetics and DevelopmentShanghai Jiaotong UniversityShanghaiChina

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