| Literature DB >> 29380326 |
Steve F C Hawkins1, Paul C Guest2.
Abstract
The emergence of next-generation sequencing (NGS) over the last 10 years has increased the efficiency of DNA sequencing in terms of speed, ease, and price. However, the exact quantification of a NGS library is crucial in order to obtain good data on sequencing platforms developed by the current market leader Illumina. Different approaches for DNA quantification are available currently and the most commonly used are based on analysis of the physical properties of the DNA through spectrophotometric or fluorometric methods. Although these methods are technically simple, they do not allow exact quantification as can be achieved using a real-time quantitative PCR (qPCR) approach. A qPCR protocol for DNA quantification with applications in NGS library preparation studies is presented here. This can be applied in various fields of study such as medical disorders resulting from nutritional programming disturbances.Keywords: Next-generation sequencing; Primers; RNA; Template; qPCR
Mesh:
Year: 2018 PMID: 29380326 DOI: 10.1007/978-1-4939-7614-0_23
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745