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Allele-specific transcription factor binding to common and rare variants associated with disease and gene expression
Genome-wide association studies (GWAS) have identified a large number of disease-associated SNPs, but in few cases the functional variant and the gene it controls have been identified. To systematically identify candidate regulatory variants, we sequenced ENCODE cell lines and used public ChIP-seq d...
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| Publicat a: | Hum Genet |
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| Autors principals: | , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer Berlin Heidelberg
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4835527/ https://ncbi.nlm.nih.gov/pubmed/26993500 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-016-1654-x |
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