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>.
| Version: | 1.0.2 |
| Depends: | R (≥ 3.5) |
| Imports: | BEDMatrix (≥ 2.0.3),checkmate (≥ 2.0.0),data.table (≥1.5.0),foreach (≥ 1.5.2),iterators (≥ 1.0.14),survival (≥3.3.1) |
| Suggests: | doParallel (≥ 1.0.17),knitr,rmarkdown,testthat (≥3.1.0),qs (≥ 0.25.2) |
| Published: | 2023-03-26 |
| DOI: | 10.32614/CRAN.package.phers |
| Author: | Jake Hughey [aut, cre], Layla Aref [aut] |
| Maintainer: | Jake Hughey <jakejhughey at gmail.com> |
| License: | GPL-2 |
| URL: | https://phers.hugheylab.org,https://github.com/hugheylab/phers |
| NeedsCompilation: | no |
| Materials: | NEWS |
| CRAN checks: | phers results |