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MEGA-V: detection of variant gene sets in patient cohorts
SUMMARY: Detecting significant associations between genetic variants and disease may prove particularly challenging when the variants are rare in the population and/or act together with other variants to cause the disease. We have developed a statistical framework named Mutation Enrichment Gene set...
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| Publicat a: | Bioinformatics |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5408849/ https://ncbi.nlm.nih.gov/pubmed/28003259 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btw809 |
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