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SNP set analysis for detecting disease association using exon sequence data
Rare variants are believed to play an important role in disease etiology. Recent advances in high-throughput sequencing technology enable investigators to systematically characterize the genetic effects of both common and rare variants. We introduce several approaches that simultaneously test the ef...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2011
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287933/ https://www.ncbi.nlm.nih.gov/pubmed/22373133 http://dx.doi.org/10.1186/1753-6561-5-S9-S91 |