Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data

Accurate detection of copy number alterations (CNAs) using next-generation sequencing technology is essential for the development and application of more precise medical treatments for human cancer. Here, we evaluated seven CNA estimation tools (ExomeCNV, CoNIFER, VarScan2, CODEX, ngCGH, saasCNV, an...

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Detalles Bibliográficos
Autores principales: Kim, Hyung-Yong, Choi, Jin-Woo, Lee, Jeong-Yeon, Kong, Gu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432334/
https://www.ncbi.nlm.nih.gov/pubmed/28460482
http://dx.doi.org/10.18632/oncotarget.15932

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432334/
https://www.ncbi.nlm.nih.gov/pubmed/28460482
http://dx.doi.org/10.18632/oncotarget.15932

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