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Comparison of scoring methods for the detection of causal genes with or without rare variants
Rare causal variants are believed to significantly contribute to the genetic basis of common diseases or quantitative traits. Appropriate statistical methods are required to discover the highest possible number of disease-relevant variants in a genome-wide screening study. The publicly available Gen...
| 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/PMC3287886/ https://www.ncbi.nlm.nih.gov/pubmed/22373454 http://dx.doi.org/10.1186/1753-6561-5-S9-S49 |