HPMPdb: A machine learning-ready database of protein molecular phenotypes associated to human missense variants

Current human Single Amino acid Variants (SAVs) databases provide a link between a SAVs and their effect on the carrier individual phenotype, often dividing them into Deleterious/Neutral variants. This is a very coarse-grained description of the genotype-to-phenotype relationship because it relies o...

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Detalles Bibliográficos
Autores principales: Raimondi, Daniele, Codicè, Francesco, Orlando, Gabriele, Schymkowitz, Joost, Rousseau, Frederic, Moreau, Yves
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166469/
https://www.ncbi.nlm.nih.gov/pubmed/35669450
http://dx.doi.org/10.1016/j.crstbi.2022.04.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166469/
https://www.ncbi.nlm.nih.gov/pubmed/35669450
http://dx.doi.org/10.1016/j.crstbi.2022.04.004

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