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...
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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BMC
2024-03-01
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| Series: | BMC Bioinformatics |
| Assuntos: | |
| Acceso en liña: | https://doi.org/10.1186/s12859-024-05709-6 |
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