| Literature DB >> 31267764 |
Fleur Hammet1,2, Khalid Mahmood3,2, Thomas R Green3, Tu Nguyen-Dumont1,4, Melissa C Southey1,4,5, Daniel D Buchanan3, Andrew Lonie2, Katherine L Nathanson6, Fergus J Couch7, Bernard J Pope3,2, Daniel J Park1,2.
Abstract
We have previously reported Hi-Plex, a multiplex PCR methodology for building targeted DNA sequencing libraries that offers a low-cost protocol compatible with high-throughput processing. Here, we detail an improved protocol, Hi-Plex2, that more effectively enables the robust construction of small-to-medium panel-size libraries while maintaining low cost, simplicity and accuracy benefits of the Hi-Plex platform. Hi-Plex2 was applied to three panels, comprising 291, 740 and 1193 amplicons, targeting genes associated with risk for breast and/or colon cancer. We show substantial reduction of off-target amplification to enable library construction for small-to-medium-sized design panels not possible using the previous Hi-Plex chemistry.Entities:
Keywords: Hi-Plex; genetic screening; multiplex PCR; targeted DNA sequencing; variant detection
Mesh:
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Year: 2019 PMID: 31267764 DOI: 10.2144/btn-2019-0026
Source DB: PubMed Journal: Biotechniques ISSN: 0736-6205 Impact factor: 1.993