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: |
0.0.3 |
| Depends: |
R (≥ 3.5) |
| Imports: |
checkmate (≥ 2.0.0), data.table (≥ 1.5.0), foreach (≥
1.5.2), iterators (≥ 1.0.14), BEDMatrix (≥ 2.0.3) |
| Suggests: |
doParallel (≥ 1.0.17), knitr, rmarkdown, testthat (≥
3.1.0), qs (≥ 0.25.2) |
| Published: |
2022-05-31 |
| 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 |