| Literature DB >> 23933242 |
Tú Nguyen-Dumont1, Bernard J Pope, Fleur Hammet, Maryam Mahmoodi, Helen Tsimiklis, Melissa C Southey, Daniel J Park.
Abstract
Although per-base sequencing costs have decreased during recent years, library preparation for targeted massively parallel sequencing remains constrained by high reagent cost, limited design flexibility, and protocol complexity. To address these limitations, we previously developed Hi-Plex, a polymerase chain reaction (PCR) massively parallel sequencing strategy for screening panels of genomic target regions. Here, we demonstrate that Hi-Plex applied with hybrid adapters can generate a library suitable for sequencing with both the Ion Torrent and the TruSeq chemistries and that adjusting primer concentrations improves coverage uniformity. These results expand Hi-Plex capabilities as an accurate, affordable, flexible, and rapid approach for various genetic screening applications.Entities:
Keywords: Disease gene screening; High-Plex PCR; Massively parallel sequencing; Molecular diagnostics; Targeted sequencing
Mesh:
Year: 2013 PMID: 23933242 PMCID: PMC3839948 DOI: 10.1016/j.ab.2013.07.046
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365