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Enlight: web-based integration of GWAS results with biological annotations
Summary: Identifying causal variants remains a key challenge in post-GWAS (genome-wide association study) era, as many GWAS single-nucleotide polymorphisms (SNPs) (including imputed ones) fall into non-coding regions, making it difficult to associate statistical significance with predicted functiona...
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| Publicat a: | Bioinformatics |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4287951/ https://ncbi.nlm.nih.gov/pubmed/25262152 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btu639 |
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