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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2018
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| Materias: | |
| 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 |