cnvScan: a CNV screening and annotation tool to improve the clinical utility of computational CNV prediction from exome sequencing data

BACKGROUND: With advances in next generation sequencing technology and analysis methods, single nucleotide variants (SNVs) and indels can be detected with high sensitivity and specificity in exome sequencing data. Recent studies have demonstrated the ability to detect disease-causing copy number var...

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Detalles Bibliográficos
Autores principales: Samarakoon, Pubudu Saneth, Sorte, Hanne Sørmo, Stray-Pedersen, Asbjørg, Rødningen, Olaug Kristin, Rognes, Torbjørn, Lyle, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712464/
https://www.ncbi.nlm.nih.gov/pubmed/26764020
http://dx.doi.org/10.1186/s12864-016-2374-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712464/
https://www.ncbi.nlm.nih.gov/pubmed/26764020
http://dx.doi.org/10.1186/s12864-016-2374-2

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