Comparative analysis of copy number variation detection methods and database construction

BACKGROUND: Array-based detection of copy number variations (CNVs) is widely used for identifying disease-specific genetic variations. However, the accuracy of CNV detection is not sufficient and results differ depending on the detection programs used and their parameters. In this study, we evaluate...

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Detalles Bibliográficos
Autores principales: Koike, Asako, Nishida, Nao, Yamashita, Daiki, Tokunaga, Katsushi
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3058066/
https://www.ncbi.nlm.nih.gov/pubmed/21385384
http://dx.doi.org/10.1186/1471-2156-12-29

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3058066/
https://www.ncbi.nlm.nih.gov/pubmed/21385384
http://dx.doi.org/10.1186/1471-2156-12-29

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