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

Abstract 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 wi...

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Bibliographic Details
Main Authors: F. Genova, M. Longeri, L. A. Lyons, A. Bagnato, the 99Lives Consortium, M. G. Strillacci
Format: Article
Language:English
Published: BMC 2018-12-01
Series:BMC Genomics
Subjects:
CNV
NGS
Online Access:http://link.springer.com/article/10.1186/s12864-018-5297-2