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 |
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-devel (arm64): phers_1.0.2.tgz, r-release (arm64): phers_1.0.2.tgz, r-oldrel (arm64): phers_1.0.2.tgz, r-devel (x86_64): 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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