CNV-seq, a new method to detect copy number variation using high-throughput sequencing

BACKGROUND: DNA copy number variation (CNV) has been recognized as an important source of genetic variation. Array comparative genomic hybridization (aCGH) is commonly used for CNV detection, but the microarray platform has a number of inherent limitations. RESULTS: Here, we describe a method to det...

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Detalles Bibliográficos
Autores principales: Xie, Chao, Tammi, Martti T
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667514/
https://www.ncbi.nlm.nih.gov/pubmed/19267900
http://dx.doi.org/10.1186/1471-2105-10-80

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667514/
https://www.ncbi.nlm.nih.gov/pubmed/19267900
http://dx.doi.org/10.1186/1471-2105-10-80

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