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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Veröffentlicht in:Genes Chromosomes Cancer
Hauptverfasser: 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
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2018
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Article
Online Zugang: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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