Routines to simulate and manipulate pedigrees ascertained to contain multiple family members affected by a rare disease. Christina Nieuwoudt, Samantha J Jones, Angela Brooks-Wilson, and Jinko Graham (2018) <doi:10.1101/234153>.
Version: | 0.3.0 |
Depends: | R (≥ 3.4.0) |
Imports: | kinship2 (≥ 1.6.4), dplyr (≥ 0.7.4), stats (≥ 3.4.0) |
Suggests: | doParallel (≥ 1.0.11), doRNG (≥ 1.6.6), graphics (≥ 3.4.0), knitr (≥ 1.17), rmarkdown (≥ 1.8), roxygen2 (≥ 6.0.1), testthat (≥ 2.0.0) |
Published: | 2018-10-01 |
Author: | Christina Nieuwoudt [aut, cre], Jinko Graham [aut] |
Maintainer: | Christina Nieuwoudt <cnieuwou at sfu.ca> |
License: | GPL-2 | GPL-3 [expanded from: GNU General Public License] |
NeedsCompilation: | no |
CRAN checks: | SimRVPedigree results |
Reference manual: | SimRVPedigree.pdf |
Vignettes: |
SimRVPedigree |
Package source: | SimRVPedigree_0.3.0.tar.gz |
Windows binaries: | r-devel: SimRVPedigree_0.3.0.zip, r-release: SimRVPedigree_0.3.0.zip, r-oldrel: SimRVPedigree_0.3.0.zip |
OS X binaries: | r-release: SimRVPedigree_0.3.0.tgz, r-oldrel: SimRVPedigree_0.3.0.tgz |
Old sources: | SimRVPedigree archive |
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