ExCNVSS: A Noise-Robust Method for Copy Number Variation Detection in Whole Exome Sequencing Data

Copy number variations (CNVs) are structural variants associated with human diseases. Recent studies verified that disease-related genes are based on the extraction of rare de novo and transmitted CNVs from exome sequencing data. The need for more efficient and accurate methods has increased, which...

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Detalles Bibliográficos
Autores principales: Kong, Jinhwa, Shin, Jaemoon, Won, Jungim, Lee, Keonbae, Lee, Unjoo, Yoon, Jeehee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494116/
https://www.ncbi.nlm.nih.gov/pubmed/28698882
http://dx.doi.org/10.1155/2017/9631282

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494116/
https://www.ncbi.nlm.nih.gov/pubmed/28698882
http://dx.doi.org/10.1155/2017/9631282

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