Quantifying single nucleotide variant detection sensitivity in exome sequencing

BACKGROUND: The targeted capture and sequencing of genomic regions has rapidly demonstrated its utility in genetic studies. Inherent in this technology is considerable heterogeneity of target coverage and this is expected to systematically impact our sensitivity to detect genuine polymorphisms. To f...

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Detalles Bibliográficos
Autores principales: Meynert, Alison M, Bicknell, Louise S, Hurles, Matthew E, Jackson, Andrew P, Taylor, Martin S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695811/
https://www.ncbi.nlm.nih.gov/pubmed/23773188
http://dx.doi.org/10.1186/1471-2105-14-195

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695811/
https://www.ncbi.nlm.nih.gov/pubmed/23773188
http://dx.doi.org/10.1186/1471-2105-14-195

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