Accurate variant detection across non-amplified and whole genome amplified DNA using targeted next generation sequencing

BACKGROUND: Many hypothesis-driven genetic studies require the ability to comprehensively and efficiently target specific regions of the genome to detect sequence variations. Often, sample availability is limited requiring the use of whole genome amplification (WGA). We evaluated a high-throughput m...

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Bibliografski detalji
Glavni autori: ElSharawy, Abdou, Warner, Jason, Olson, Jeff, Forster, Michael, Schilhabel, Markus B, Link, Darren R, Rose-John, Stefan, Schreiber, Stefan, Rosenstiel, Philip, Brayer, James, Franke, Andre
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2012
Teme:
Methodology Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3534403/
https://ncbi.nlm.nih.gov/pubmed/22994565
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-13-500
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