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Testing Rare Variants for Association with Diseases: a Bayesian Marker Selection Approach
It has been a research focus to uncover the genetic determination of complex diseases caused by rare variants. As the vast majority of genomic variants represent background variation, highlighting potentially causal mutations through weighting scheme is critical to the success of rare variants aimed...
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| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2011
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3242831/ https://ncbi.nlm.nih.gov/pubmed/22034989 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-1809.2011.00684.x |
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