RefCNV: Identification of Gene-Based Copy Number Variants Using Whole Exome Sequencing

With rapid advances in DNA sequencing technologies, whole exome sequencing (WES) has become a popular approach for detecting somatic mutations in oncology studies. The initial intent of WES was to characterize single nucleotide variants, but it was observed that the number of sequencing reads that m...

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Detalles Bibliográficos
Autores principales: Chang, Lun-Ching, Das, Biswajit, Lih, Chih-Jian, Si, Han, Camalier, Corinne E., McGregor, Paul M., Polley, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2016
Materias:
Methodology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849420/
https://www.ncbi.nlm.nih.gov/pubmed/27147817
http://dx.doi.org/10.4137/CIN.S36612

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849420/
https://www.ncbi.nlm.nih.gov/pubmed/27147817
http://dx.doi.org/10.4137/CIN.S36612

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