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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...
Autores principales: | Oldridge, Derek A., Banerjee, Samprit, Setlur, Sunita R., Sboner, Andrea, Demichelis, Francesca |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2879534/ https://www.ncbi.nlm.nih.gov/pubmed/20156996 http://dx.doi.org/10.1093/nar/gkq073 |
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