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Exome-wide rare variant analyses of two bone mineral density phenotypes: the challenges of analyzing rare genetic variation
Performance of a recently developed test for association between multivariate phenotypes and sets of genetic variants (MURAT) is demonstrated using measures of bone mineral density (BMD). By combining individual-level whole genome sequenced data from the UK10K study, and imputed genome-wide genetic...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group UK
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760616/ https://www.ncbi.nlm.nih.gov/pubmed/29317680 http://dx.doi.org/10.1038/s41598-017-18385-9 |