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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...
Tallennettuna:
| Julkaisussa: | Nat Genet |
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| Päätekijät: | , , , , , , , , , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7611956/ https://ncbi.nlm.nih.gov/pubmed/34711957 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41588-021-00945-5 |
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