Ładuje się......
CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics
BACKGROUND: Recent studies have shown that copy number variations (CNVs) are frequent in higher eukaryotes and associated with a substantial portion of inherited and acquired risk for various human diseases. The increasing availability of high-resolution genome surveillance platforms provides opport...
Zapisane w:
| Główni autorzy: | , , , , , , , , , |
|---|---|
| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
BioMed Central
2010
|
| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2827374/ https://ncbi.nlm.nih.gov/pubmed/20132550 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-11-74 |
| Etykiety: |
Dodaj etykietę
Nie ma etykietki, Dołącz pierwszą etykiete!
|