hugheylab/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>.
Getting started
Browse package contents
Package details |
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| Maintainer | |
| License | GPL-2 |
| Version | 1.0.2 |
| URL | https://phers.hugheylab.org https://github.com/hugheylab/phers |
| Package repository | View on GitHub |
| Installation |
Install the latest version of this package by entering the following in R:
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