A Multi-Sample Based Method for Identifying Common CNVs in Normal Human Genomic Structure Using High-Resolution aCGH Data

BACKGROUND: It is difficult to identify copy number variations (CNV) in normal human genomic data due to noise and non-linear relationships between different genomic regions and signal intensity. A high-resolution array comparative genomic hybridization (aCGH) containing 42 million probes, which is...

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Detalles Bibliográficos
Autores principales: Park, Chihyun, Ahn, Jaegyoon, Yoon, Youngmi, Park, Sanghyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205051/
https://www.ncbi.nlm.nih.gov/pubmed/22073121
http://dx.doi.org/10.1371/journal.pone.0026975

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205051/
https://www.ncbi.nlm.nih.gov/pubmed/22073121
http://dx.doi.org/10.1371/journal.pone.0026975

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