DeviCNV: detection and visualization of exon-level copy number variants in targeted next-generation sequencing data

BACKGROUND: Targeted next-generation sequencing (NGS) is increasingly being adopted in clinical laboratories for genomic diagnostic tests. RESULTS: We developed a new computational method, DeviCNV, intended for the detection of exon-level copy number variants (CNVs) in targeted NGS data. DeviCNV bui...

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Detalles Bibliográficos
Autores principales: Kang, Yeeok, Nam, Seong-Hyeuk, Park, Kyung Sun, Kim, Yoonjung, Kim, Jong-Won, Lee, Eunjung, Ko, Jung Min, Lee, Kyung-A, Park, Inho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192323/
https://www.ncbi.nlm.nih.gov/pubmed/30326846
http://dx.doi.org/10.1186/s12859-018-2409-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192323/
https://www.ncbi.nlm.nih.gov/pubmed/30326846
http://dx.doi.org/10.1186/s12859-018-2409-6

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