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Incorporating Linkage Information into a Common Disease/Rare Variant Framework
Recent developments in sequencing technology have allowed the investigation of the common disease/rare variant hypothesis. In the Genetic Analysis Workshop 17 data set, we have sequence data on both unrelated individuals and eight large extended pedigrees with simulated quantitative and qualitative...
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| I publikationen: | Genet Epidemiol |
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| Huvudupphovsmän: | , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2011
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4558895/ https://ncbi.nlm.nih.gov/pubmed/22128063 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.20654 |
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