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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2012
Gaiak:
Methodology Article
Sarrera elektronikoa: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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