| Literature DB >> 24502796 |
Steven R Head1, H Kiyomi Komori2, Sarah A LaMere2, Thomas Whisenant2, Filip Van Nieuwerburgh3, Daniel R Salomon2, Phillip Ordoukhanian1.
Abstract
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.Entities:
Keywords: ChIP-seq; DNA; DNA-seq; RIP-seq; RNA; RNA-seq; deep sequencing; library preparation; next-generation sequencing
Mesh:
Year: 2014 PMID: 24502796 PMCID: PMC4351865 DOI: 10.2144/000114133
Source DB: PubMed Journal: Biotechniques ISSN: 0736-6205 Impact factor: 1.993