Genome-Wide Mapping of Copy Number Variation in Humans: Comparative Analysis of High Resolution Array Platforms

Accurate and efficient genome-wide detection of copy number variants (CNVs) is essential for understanding human genomic variation, genome-wide CNV association type studies, cytogenetics research and diagnostics, and independent validation of CNVs identified from sequencing based technologies. Numer...

Descripción completa

Detalles Bibliográficos
Autores principales: Haraksingh, Rajini R., Abyzov, Alexej, Gerstein, Mark, Urban, Alexander E., Snyder, Michael
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/PMC3227574/
https://www.ncbi.nlm.nih.gov/pubmed/22140474
http://dx.doi.org/10.1371/journal.pone.0027859

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3227574/
https://www.ncbi.nlm.nih.gov/pubmed/22140474
http://dx.doi.org/10.1371/journal.pone.0027859

Ejemplares similares