DVA: predicting the functional impact of single nucleotide missense variants
Abstract Background In the past decade, single nucleotide variants (SNVs) have been identified as having a significant relationship with the development and treatment of diseases. Among them, prioritizing missense variants for further functional impact investigation is an essential challenge in the...
Enregistré dans:
| Auteurs principaux: | , , , |
|---|---|
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BMC
2024-03-01
|
| Collection: | BMC Bioinformatics |
| Sujets: | |
| Accès en ligne: | https://doi.org/10.1186/s12859-024-05709-6 |
| Tags: |
Pas de tags, Soyez le premier à ajouter un tag!
|