Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts

Understanding the impact of rare variants is essential to understanding human health. We analyze rare (MAF < 0.1%) variants against 4264 phenotypes in 49,960 exome-sequenced individuals from the UK Biobank and 1934 phenotypes (1821 overlapping with UK Biobank) in 21,866 members of the Healthy Nev...

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Detalles Bibliográficos
Autores principales: Cirulli, Elizabeth T., White, Simon, Read, Robert W., Elhanan, Gai, Metcalf, William J., Tanudjaja, Francisco, Fath, Donna M., Sandoval, Efren, Isaksson, Magnus, Schlauch, Karen A., Grzymski, Joseph J., Lu, James T., Washington, Nicole L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6987107/
https://www.ncbi.nlm.nih.gov/pubmed/31992710
http://dx.doi.org/10.1038/s41467-020-14288-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6987107/
https://www.ncbi.nlm.nih.gov/pubmed/31992710
http://dx.doi.org/10.1038/s41467-020-14288-y

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