SNPnexus: assessing the functional relevance of genetic variation to facilitate the promise of precision medicine

Broader functional annotation of genetic variation is a valuable means for prioritising phenotypically-important variants in further disease studies and large-scale genotyping projects. We developed SNPnexus to meet this need by assessing the potential significance of known and novel SNPs on the maj...

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Detalles Bibliográficos
Autores principales: Dayem Ullah, Abu Z, Oscanoa, Jorge, Wang, Jun, Nagano, Ai, Lemoine, Nicholas R, Chelala, Claude
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Web Server Issue
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030955/
https://www.ncbi.nlm.nih.gov/pubmed/29757393
http://dx.doi.org/10.1093/nar/gky399

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030955/
https://www.ncbi.nlm.nih.gov/pubmed/29757393
http://dx.doi.org/10.1093/nar/gky399

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