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DIVAS: a centralized genetic variant repository representing 150 000 individuals from multiple disease cohorts
Motivation: A plethora of sequenced and genotyped disease cohorts is available to the biomedical research community, spread across many portals and represented in various formats. Results: We have gathered several large studies, including GERA and GRU, and computed population- and disease-specific g...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2016
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681987/ https://www.ncbi.nlm.nih.gov/pubmed/26363178 http://dx.doi.org/10.1093/bioinformatics/btv511 |