4.3 Article

Library construction for next-generation sequencing: Overviews and challenges

Journal

BIOTECHNIQUES
Volume 56, Issue 2, Pages 61-+

Publisher

FUTURE SCI LTD
DOI: 10.2144/000114133

Keywords

deep sequencing; DNA; RNA; library preparation; next-generation sequencing; RNA-seq; DNA-seq; ChIP-seq; RIP-seq

Funding

  1. NIH [R24 GM09879, U19 A1063603, U01 GM094653, U01 AI084146, U54 A1008353]
  2. JDRF postdoctoral fellowship

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High-throughput sequencing, also known as next-generation sequencing (NGS), has revolutionized genomic research. In recent years, NGS technology has steadily improved, with costs dropping and the number and range of sequencing applications increasing exponentially. Here, we examine the critical role of sequencing library quality and consider important challenges when preparing NGS libraries from DNA and RNA sources. Factors such as the quantity and physical characteristics of the RNA or DNA source material as well as the desired application (i.e., genome sequencing, targeted sequencing, RNA-seq, ChIP-seq, RIP-seq, and methylation) are addressed in the context of preparing high quality sequencing libraries. In addition, the current methods for preparing NGS libraries from single cells are also discussed.

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