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Use phenotype risk scores based on linked clinical and genetic data to study Mendelian disease and rare genetic variants. See Bastarache et al. 2018 <doi:10.1126/science.aal4043>.
Package details |
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Author | Jake Hughey [aut, cre], Layla Aref [aut] |
Maintainer | Jake Hughey <jakejhughey@gmail.com> |
License | GPL-2 |
Version | 1.0.2 |
URL | https://phers.hugheylab.org https://github.com/hugheylab/phers |
Package repository | View on CRAN |
Installation |
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