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ncVarDB: a manually curated database for pathogenic non-coding variants and benign controls
Variants within the non-coding genome are frequently associated with phenotypes in genome-wide association studies. These non-coding regions may be involved in the regulation of gene expression, encode functional non-coding RNAs, or influence splicing and other cellular functions. We have curated a...
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| Publicat a: | Database (Oxford) |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7706182/ https://ncbi.nlm.nih.gov/pubmed/33258967 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/database/baaa105 |
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