In silico methods for predicting functional synonymous variants

Single nucleotide variants (SNVs) contribute to human genomic diversity. Synonymous SNVs are previously considered to be “silent,” but mounting evidence has revealed that these variants can cause RNA and protein changes and are implicated in over 85 human diseases and cancers. Recent improvements in...

Descripción completa

Detalles Bibliográficos
Autores principales: Lin, Brian C., Katneni, Upendra, Jankowska, Katarzyna I., Meyer, Douglas, Kimchi-Sarfaty, Chava
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10204308/
https://www.ncbi.nlm.nih.gov/pubmed/37217943
http://dx.doi.org/10.1186/s13059-023-02966-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10204308/
https://www.ncbi.nlm.nih.gov/pubmed/37217943
http://dx.doi.org/10.1186/s13059-023-02966-1

Ejemplares similares