Massive screening of copy number population-scale variation in Bos taurus genome

BACKGROUND: Copy number variations (CNVs) represent a significant source of genomic structural variation. Their length ranges from approximately one hundred to millions of base pair. Genome-wide screenings have clarified that CNVs are a ubiquitous phenomenon affecting essentially the whole genome. A...

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Detalles Bibliográficos
Autores principales: Cicconardi, Francesco, Chillemi, Giovanni, Tramontano, Anna, Marchitelli, Cinzia, Valentini, Alessio, Ajmone-Marsan, Paolo, Nardone, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3618309/
https://www.ncbi.nlm.nih.gov/pubmed/23442185
http://dx.doi.org/10.1186/1471-2164-14-124

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3618309/
https://www.ncbi.nlm.nih.gov/pubmed/23442185
http://dx.doi.org/10.1186/1471-2164-14-124

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