Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets

Somatic copy number variations (CNVs) play a crucial role in development of many human cancers. The broad availability of next-generation sequencing data has enabled the development of algorithms to computationally infer CNV profiles from a variety of data types including exome and targeted sequence...

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Detalles Bibliográficos
Autores principales: Samadian, Soroush, Bruce, Jeff P., Pugh, Trevor J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5891060/
https://www.ncbi.nlm.nih.gov/pubmed/29590101
http://dx.doi.org/10.1371/journal.pcbi.1006080

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5891060/
https://www.ncbi.nlm.nih.gov/pubmed/29590101
http://dx.doi.org/10.1371/journal.pcbi.1006080

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