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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...

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Detalhes bibliográficos
Main Authors: Ju, Young Seok, Hong, Dongwan, Kim, Sheehyun, Park, Sung-Soo, Kim, Sujung, Lee, Seungbok, Park, Hansoo, Kim, Jong-Il, Seo, Jeong-Sun
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2978381/
https://ncbi.nlm.nih.gov/pubmed/20802225
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkq730
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