Literature DB >> 29380326

Rapid and Easy Protocol for Quantification of Next-Generation Sequencing Libraries.

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


  1 in total

1.  Isolation of high-quality total RNA and RNA sequencing of single bovine oocytes.

Authors:  Fernando H Biase
Journal:  STAR Protoc       Date:  2021-10-19
  1 in total

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