Učitavanje...
In Vivo Functional Study of Disease-Associated Rare Human Variants using Drosophila
Advances in sequencing technology have made whole-genome and whole-exome datasets more accessible for both clinical diagnosis and cutting-edge human genetics research. Although a number of in silico algorithms have been developed to predict the pathogenicity of variants identified in these datasets,...
Spremljeno u:
| Izdano u: | J Vis Exp |
|---|---|
| Glavni autori: | , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2019
|
| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7418855/ https://ncbi.nlm.nih.gov/pubmed/31498321 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3791/59658 |
| Oznake: |
Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!
|