Estimating copy numbers of alleles from population-scale high-throughput sequencing data

BACKGROUND: With the recent development of microarray and high-throughput sequencing (HTS) technologies, a number of studies have revealed catalogs of copy number variants (CNVs) and their association with phenotypes and complex traits. In parallel, a number of approaches to predict CNV regions and...

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Detalles Bibliográficos
Autores principales: Mimori, Takahiro, Nariai, Naoki, Kojima, Kaname, Sato, Yukuto, Kawai, Yosuke, Yamaguchi-Kabata, Yumi, Nagasaki, Masao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331703/
https://www.ncbi.nlm.nih.gov/pubmed/25707811
http://dx.doi.org/10.1186/1471-2105-16-S1-S4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331703/
https://www.ncbi.nlm.nih.gov/pubmed/25707811
http://dx.doi.org/10.1186/1471-2105-16-S1-S4

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