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Optimizing copy number variation analysis using genome-wide short sequence oligonucleotide arrays
The detection of copy number variants (CNV) by array-based platforms provides valuable insight into understanding human diversity. However, suboptimal study design and data processing negatively affect CNV assessment. We quantitatively evaluate their impact when short-sequence oligonucleotide arrays...
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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/PMC2879534/ https://ncbi.nlm.nih.gov/pubmed/20156996 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkq073 |
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