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...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2018-12-01
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Series: | BMC Genomics |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s12864-018-5297-2 |