phers
Calculate Phenotype Risk Scores
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>.
Versions across snapshots
| Version | Repository | File | Size |
|---|---|---|---|
1.0.5 |
rolling linux/jammy R-4.5 | phers_1.0.5.tar.gz |
1.8 MiB |
1.0.5 |
rolling linux/noble R-4.5 | phers_1.0.5.tar.gz |
1.8 MiB |
1.0.5 |
rolling source/ R- | phers_1.0.5.tar.gz |
1.4 MiB |
1.0.5 |
latest linux/jammy R-4.5 | phers_1.0.5.tar.gz |
1.8 MiB |
1.0.5 |
latest linux/noble R-4.5 | phers_1.0.5.tar.gz |
1.8 MiB |
1.0.5 |
latest source/ R- | phers_1.0.5.tar.gz |
1.4 MiB |
1.0.5 |
2026-04-26 source/ R- | phers_1.0.5.tar.gz |
1.4 MiB |
1.0.5 |
2026-04-23 source/ R- | phers_1.0.5.tar.gz |
1.4 MiB |
1.0.5 |
2026-04-09 windows/windows R-4.5 | phers_1.0.5.zip |
1.8 MiB |
1.0.2 |
2025-04-20 source/ R- | phers_1.0.2.tar.gz |
1.4 MiB |
Dependencies (latest)
Imports
Suggests
- doParallel (>= 1.0.17)
- knitr
- rmarkdown
- testthat (>= 3.1.0)