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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Bibliografski detalji
Glavni autori: Ju, Young Seok, Hong, Dongwan, Kim, Sheehyun, Park, Sung-Soo, Kim, Sujung, Lee, Seungbok, Park, Hansoo, Kim, Jong-Il, Seo, Jeong-Sun
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2010
Teme:
Methods Online
Online pristup: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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