| Literature DB >> 23994687 |
P Gyarmati1, Y Song, J Hällman, M Käller.
Abstract
Fragmentation is essential in most library preparation protocols for use with massively parallel sequencing systems. Complexes that generate hydroxyl radicals, such as iron-EDTA, can be used to introduce random DNA cleavage. Here we describe a chemical fragmentation method that can be incorporated into library preparation protocols for next-generation sequencing workflows. This protocol has been validated by whole genome, amplicon and exome sequencing. Chemical fragmentation is a cost-effective alternative to current fragmentation methods that has no observable sequence bias and requires no instrumentation.Entities:
Keywords: Fragmentation; High-throughput sequencing; Library preparation
Mesh:
Year: 2013 PMID: 23994687 DOI: 10.1016/j.jbiotec.2013.08.020
Source DB: PubMed Journal: J Biotechnol ISSN: 0168-1656 Impact factor: 3.307