Cargando…
DIVAN: accurate identification of non-coding disease-specific risk variants using multi-omics profiles
Understanding the link between non-coding sequence variants, identified in genome-wide association studies, and the pathophysiology of complex diseases remains challenging due to a lack of annotations in non-coding regions. To overcome this, we developed DIVAN, a novel feature selection and ensemble...
| Autores principales: | , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2016
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5139035/ https://www.ncbi.nlm.nih.gov/pubmed/27923386 http://dx.doi.org/10.1186/s13059-016-1112-z |