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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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| I publikationen: | Bioinformatics |
|---|---|
| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Oxford University Press
2015
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| Ämnen: | |
| Länkar: | 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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