Reference-unbiased copy number variant analysis using CGH microarrays

Comparative genomic hybridization (CGH) microarrays have been used to determine copy number variations (CNVs) and their effects on complex diseases. Detection of absolute CNVs independent of genomic variants of an arbitrary reference sample has been a critical issue in CGH array experiments. Whole g...

Descripción completa

Detalles Bibliográficos
Autores principales: Ju, Young Seok, Hong, Dongwan, Kim, Sheehyun, Park, Sung-Soo, Kim, Sujung, Lee, Seungbok, Park, Hansoo, Kim, Jong-Il, Seo, Jeong-Sun
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978381/
https://www.ncbi.nlm.nih.gov/pubmed/20802225
http://dx.doi.org/10.1093/nar/gkq730

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978381/
https://www.ncbi.nlm.nih.gov/pubmed/20802225
http://dx.doi.org/10.1093/nar/gkq730

Ejemplares similares