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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 |
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-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 |
Please use the canonical form https://CRAN.R-project.org/package=phers to link to this page.
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.