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Identifying causal regulatory SNPs in ChIP-seq enhancers
Thousands of non-coding SNPs have been linked to human diseases in the past. The identification of causal alleles within this pool of disease-associated non-coding SNPs is largely impossible due to the inability to accurately quantify the impact of non-coding variation. To overcome this challenge, w...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4288203/ https://www.ncbi.nlm.nih.gov/pubmed/25520196 http://dx.doi.org/10.1093/nar/gku1318 |