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Enrichment analysis of genetic association in genes and pathways by aggregating signals from both rare and common variants
New high-throughput sequencing technologies have brought forth opportunities for unbiased analysis of thousands of rare genomic variants in genome-wide association studies of complex diseases. Because it is hard to detect single rare variants with appreciable effect sizes at the population level, ex...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2011
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287890/ https://www.ncbi.nlm.nih.gov/pubmed/22373052 http://dx.doi.org/10.1186/1753-6561-5-S9-S52 |