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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Detalles Bibliográficos
Autores principales: Oldridge, Derek A., Banerjee, Samprit, Setlur, Sunita R., Sboner, Andrea, Demichelis, Francesca
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Genomics
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

Internet

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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