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Comparison of collapsing methods for the statistical analysis of rare variants
Novel technologies allow sequencing of whole genomes and are considered as an emerging approach for the identification of rare disease-associated variants. Recent studies have shown that multiple rare variants can explain a particular proportion of the genetic basis for disease. Following this assum...
| 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/PMC3287839/ https://www.ncbi.nlm.nih.gov/pubmed/22373249 http://dx.doi.org/10.1186/1753-6561-5-S9-S115 |