An evaluation of copy number variation detection tools for cancer using whole exome sequencing data

BACKGROUND: Recently copy number variation (CNV) has gained considerable interest as a type of genomic/genetic variation that plays an important role in disease susceptibility. Advances in sequencing technology have created an opportunity for detecting CNVs more accurately. Recently whole exome sequ...

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Detalles Bibliográficos
Autores principales: Zare, Fatima, Dow, Michelle, Monteleone, Nicholas, Hosny, Abdelrahman, Nabavi, Sheida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452530/
https://www.ncbi.nlm.nih.gov/pubmed/28569140
http://dx.doi.org/10.1186/s12859-017-1705-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452530/
https://www.ncbi.nlm.nih.gov/pubmed/28569140
http://dx.doi.org/10.1186/s12859-017-1705-x

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