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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

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