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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>.
| 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 |
| 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 |
| Reference manual: | phers.pdf |
| Package source: | phers_1.0.2.tar.gz |
| Windows binaries: | r-devel: phers_1.0.2.zip, r-release: phers_1.0.2.zip, r-oldrel: phers_1.0.2.zip |
| macOS binaries: | r-release (arm64): phers_1.0.2.tgz, r-oldrel (arm64): phers_1.0.2.tgz, r-release (x86_64): phers_1.0.2.tgz, r-oldrel (x86_64): phers_1.0.2.tgz |
| Old sources: | phers archive |
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These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
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