Cargando…
PhD-SNPg: updating a webserver and lightweight tool for scoring nucleotide variants
One of the primary challenges in human genetics is determining the functional impact of single nucleotide variants (SNVs) and insertion and deletions (InDels), whether coding or noncoding. In the past, methods have been created to detect disease-related single amino acid changes, but only some can a...
| Autores principales: | , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2023
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320148/ https://www.ncbi.nlm.nih.gov/pubmed/37246737 http://dx.doi.org/10.1093/nar/gkad455 |