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 resultsRetroSearch is an open source project built by @garambo | Open a GitHub Issue
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