First genome-wide CNV mapping in FELIS CATUS using next generation sequencing data

BACKGROUND: Copy Number Variations (CNVs) have becoming very significant variants, representing a major source of genomic variation. CNVs involvement in phenotypic expression and different diseases has been widely demonstrated in humans as well as in many domestic animals. However, genome wide inves...

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Detalles Bibliográficos
Autores principales: Genova, F., Longeri, M., Lyons, L. A., Bagnato, A., Strillacci, M. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288940/
https://www.ncbi.nlm.nih.gov/pubmed/30526495
http://dx.doi.org/10.1186/s12864-018-5297-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288940/
https://www.ncbi.nlm.nih.gov/pubmed/30526495
http://dx.doi.org/10.1186/s12864-018-5297-2

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