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A local haplotyping tool for use in trait association and trait prediction analyses pipelines. 'HaploVar' enables users take single nucleotide polymorphisms (SNPs) (in VCF format) and a linkage disequilibrium (LD) matrix, calculate local haplotypes and format the output to be compatible with a wide range of trait association and trait prediction tools. The local haplotypes are calculated from the LD matrix using a clustering algorithm called density-based spatial clustering of applications with noise ('DBSCAN') (Ester et al., 1996) <ISBN: 1577350049>.
Version: | 0.1.1 |
Depends: | R (≥ 4.00) |
Imports: | dplyr, tidyr, tibble, magrittr, dbscan |
Suggests: | knitr, rmarkdown |
Published: | 2025-07-21 |
DOI: | 10.32614/CRAN.package.HaploVar |
Author: | Tessa MacNish |
Maintainer: | Tessa MacNish <tessa.macnish at research.uwa.edu.au> |
License: | MIT + file LICENSE |
NeedsCompilation: | no |
CRAN checks: | HaploVar results |
Reference manual: | HaploVar.html , HaploVar.pdf |
Vignettes: |
introduction (source, R code) |
Package source: | HaploVar_0.1.1.tar.gz |
Windows binaries: | r-devel: not available, r-release: not available, r-oldrel: not available |
macOS binaries: | r-release (arm64): not available, r-oldrel (arm64): not available, r-release (x86_64): HaploVar_0.1.1.tgz, r-oldrel (x86_64): HaploVar_0.1.1.tgz |
Please use the canonical form https://CRAN.R-project.org/package=HaploVar 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.