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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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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2010
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| 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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