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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Bibliographic Details
Main Authors:	Ju, Young Seok, Hong, Dongwan, Kim, Sheehyun, Park, Sung-Soo, Kim, Sujung, Lee, Seungbok, Park, Hansoo, Kim, Jong-Il, Seo, Jeong-Sun
Format:	Artigo
Language:	Inglês
Published:	Oxford University Press 2010
Subjects:	Methods Online
Online Access:	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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Reference-unbiased copy number variant analysis using CGH microarrays

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