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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,...
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| Publicat a: | J Vis Exp |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2019
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| Matèries: | |
| Accés en línia: | 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 |
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