An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci

Genome-wide association studies (GWAS) have identified many variants associated with complex traits, but identifying the causal gene(s) is a major challenge. Here we present an open resource that provides systematic fine-mapping and gene prioritization across 133,441 published human GWAS loci. We in...

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Detalles Bibliográficos
Autores principales: Mountjoy, Edward, Schmidt, Ellen M., Carmona, Miguel, Schwartzentruber, Jeremy, Peat, Gareth, Miranda, Alfredo, Fumis, Luca, Hayhurst, James, Buniello, Annalisa, Karim, Mohd Anisul, Wright, Daniel, Hercules, Andrew, Papa, Eliseo, Fauman, Eric B., Barrett, Jeffrey C., Todd, John A., Ochoa, David, Dunham, Ian, Ghoussaini, Maya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7611956/
https://www.ncbi.nlm.nih.gov/pubmed/34711957
http://dx.doi.org/10.1038/s41588-021-00945-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7611956/
https://www.ncbi.nlm.nih.gov/pubmed/34711957
http://dx.doi.org/10.1038/s41588-021-00945-5

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