Outlier-Based Identification of Copy Number Variations Using Targeted Resequencing in a Small Cohort of Patients with Tetralogy of Fallot

Copy number variations (CNVs) are one of the main sources of variability in the human genome. Many CNVs are associated with various diseases including cardiovascular disease. In addition to hybridization-based methods, next-generation sequencing (NGS) technologies are increasingly used for CNV disco...

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Detalles Bibliográficos
Autores principales: Bansal, Vikas, Dorn, Cornelia, Grunert, Marcel, Klaassen, Sabine, Hetzer, Roland, Berger, Felix, Sperling, Silke R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3882271/
https://www.ncbi.nlm.nih.gov/pubmed/24400131
http://dx.doi.org/10.1371/journal.pone.0085375

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3882271/
https://www.ncbi.nlm.nih.gov/pubmed/24400131
http://dx.doi.org/10.1371/journal.pone.0085375

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