CNstream: A method for the identification and genotyping of copy number polymorphisms using Illumina microarrays

BACKGROUND: Understanding the genetic basis of disease risk in depth requires an exhaustive knowledge of the types of genetic variation. Very recently, Copy Number Variants (CNVs) have received much attention because of their potential implication in common disease susceptibility. Copy Number Polymo...

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Detalles Bibliográficos
Autores principales: Alonso, Arnald, Julià, Antonio, Tortosa, Raül, Canaleta, Cristina, Cañete, Juan D, Ballina, Javier, Balsa, Alejandro, Tornero, Jesús, Marsal, Sara
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098064/
https://www.ncbi.nlm.nih.gov/pubmed/20482829
http://dx.doi.org/10.1186/1471-2105-11-264

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098064/
https://www.ncbi.nlm.nih.gov/pubmed/20482829
http://dx.doi.org/10.1186/1471-2105-11-264

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