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Exploring Impact of Rare Variation in Systemic Lupus Erythematosus by a Genome Wide Imputation Approach
The importance of low frequency and rare variation in complex disease genetics is difficult to estimate in patient populations. Genome-wide association studies are therefore, underpowered to detect rare variation. We have used a combined approach of genome-wide-based imputation with a highly stringe...
Autores principales: | Martínez-Bueno, Manuel, Alarcón-Riquelme, Marta E. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399402/ https://www.ncbi.nlm.nih.gov/pubmed/30863397 http://dx.doi.org/10.3389/fimmu.2019.00258 |
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