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Approaches to the detection of recessive effects using next generation sequencing data from outbred populations
Conventional methods to analyze genome-wide association studies and whole exome or whole genome sequencing studies would be prone to overlook variants which might exert a recessive effect on risk of disease, either as homozygotes or compound heterozygotes. It is plausible that such effects may be co...
Autor principal: | Curtis, David |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685401/ https://www.ncbi.nlm.nih.gov/pubmed/23807854 http://dx.doi.org/10.2147/AABC.S44332 |
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