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Variant Set Enrichment: an R package to identify disease-associated functional genomic regions
BACKGROUND: Genetic predispositions to diseases populate the noncoding regions of the human genome. Delineating their functional basis can inform on the mechanisms contributing to disease development. However, this remains a challenge due to the poor characterization of the noncoding genome. Here, w...
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| Publicado no: | BioData Min |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5320724/ https://ncbi.nlm.nih.gov/pubmed/28239419 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13040-017-0129-5 |
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