Cargando…

CNVannotator: A Comprehensive Annotation Server for Copy Number Variation in the Human Genome

Copy number variation (CNV) is one of the most prevalent genetic variations in the genome, leading to an abnormal number of copies of moderate to large genomic regions. High-throughput technologies such as next-generation sequencing often identify thousands of CNVs involved in biological or patholog...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Min, Zhao, Zhongming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3828214/
https://www.ncbi.nlm.nih.gov/pubmed/24244640
http://dx.doi.org/10.1371/journal.pone.0080170