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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3534403/
https://www.ncbi.nlm.nih.gov/pubmed/22994565
http://dx.doi.org/10.1186/1471-2164-13-500

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3534403/
https://www.ncbi.nlm.nih.gov/pubmed/22994565
http://dx.doi.org/10.1186/1471-2164-13-500

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