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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Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2012
Assuntos:
Methodology Article
Acesso em linha: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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