The Cancermuts software package for the prioritization of missense cancer variants: a case study of AMBRA1 in melanoma

Cancer genomics and cancer mutation databases have made an available wealth of information about missense mutations found in cancer patient samples. Contextualizing by means of annotation and predicting the effect of amino acid change help identify which ones are more likely to have a pathogenic imp...

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Detalles Bibliográficos
Autores principales: Tiberti, Matteo, Di Leo, Luca, Vistesen, Mette Vixø, Kuhre, Rikke Sofie, Cecconi, Francesco, De Zio, Daniela, Papaleo, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569343/
https://www.ncbi.nlm.nih.gov/pubmed/36243772
http://dx.doi.org/10.1038/s41419-022-05318-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569343/
https://www.ncbi.nlm.nih.gov/pubmed/36243772
http://dx.doi.org/10.1038/s41419-022-05318-2

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