Lanean...
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...
Gorde:
| Argitaratua izan da: | BMC Genomics |
|---|---|
| Egile Nagusiak: | , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BioMed Central
2018
|
| Gaiak: | |
| Sarrera elektronikoa: | 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 |
| Etiketak: |
Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!
|