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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Detalhes bibliográficos
Publicado no: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 em: 2018
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Article
Acesso em linha: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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