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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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| Veröffentlicht in: | BMC Genomics |
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| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2018
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6288940/ https://ncbi.nlm.nih.gov/pubmed/30526495 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-018-5297-2 |
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