DEOGEN2: prediction and interactive visualization of single amino acid variant deleteriousness in human proteins

High-throughput sequencing methods are generating enormous amounts of genomic data, giving unprecedented insights into human genetic variation and its relation to disease. An individual human genome contains millions of Single Nucleotide Variants: to discriminate the deleterious from the benign ones...

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Detalles Bibliográficos
Autores principales: Raimondi, Daniele, Tanyalcin, Ibrahim, Ferté, Julien, Gazzo, Andrea, Orlando, Gabriele, Lenaerts, Tom, Rooman, Marianne, Vranken, Wim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Web Server Issue
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570203/
https://www.ncbi.nlm.nih.gov/pubmed/28498993
http://dx.doi.org/10.1093/nar/gkx390

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570203/
https://www.ncbi.nlm.nih.gov/pubmed/28498993
http://dx.doi.org/10.1093/nar/gkx390

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