Copy Number Variant Analysis using Genome-Wide Mate-Pair Sequencing

Copy number variation (CNV) is a common form of structural variation detected in human genomes, occurring as both constitutional and somatic events. Cytogenetic techniques like chromosomal microarray (CMA) are widely used in analyzing CNVs. However, CMA techniques cannot resolve the full nature of t...

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Publicado en:Genes Chromosomes Cancer
Main Authors: Smadbeck, James B, Johnson, Sarah H., Smoley, Stephanie A., Gaitatzes, Athanasios, Drucker, Travis M., Zenka, Roman M., Kosari, Farhad, Murphy, Stephen J., Hoppman, Nicole, Aypar, Umut, Sukov, William R., Jenkins, Robert B., Kearney, Hutton M., Feldman, Andrew L., Vasmatzis, George
Formato: Artigo
Idioma:Inglês
Publicado: 2018
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6117203/
https://ncbi.nlm.nih.gov/pubmed/29726617
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gcc.5
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