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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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| 主要な著者: | , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2010
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| 主題: | |
| オンライン･アクセス: | 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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