Write a HZAR file (Derryberry et al. 2013), from a tidy data frame. Used internally in genometranslator and might be of interest for users.
Usage
write_hzar(
data,
distances = NULL,
filename = NULL,
parallel.core = parallel::detectCores() - 1
)Arguments
- data
A tidy data frame object in the global environment or a tidy data frame in wide or long format in the working directory. How to get a tidy data frame ? Look into genometranslator
tidy_genome.- distances
(optional) A file with 2 columns,
POP_IDand the distance information per populations. With default:distances = NULL, the column is left empty. Default:distances = NULL.- filename
(optional) The file name prefix for the HZAR file written to the working directory. With default:
filename = NULL, the date and time is appended toradiator_hzar_. Default:filename = NULL.- parallel.core
Default:
parallel.core = parallel::detectCores() - 1.
Data filtering
This writer does not silently filter markers or individuals. It may validate requirements imposed by the destination format and stop with an informative error when the input is unsuitable. It is the user's responsibility to filter and quality-control the data appropriately for the intended analysis before generating the output. Use radr or another suitable workflow when filtering is required.
Dependencies
Required package dependencies are declared in DESCRIPTION and are
installed with genometranslator. Any additional dependency needed only
for this format or option is identified in this help page. Use
genometranslator_dependencies() to inspect the availability of core
packages, optional packages, and external executables.
References
Derryberry EP, Derryberry GE, Maley JM, Brumfield RT. hzar: hybrid zone analysis using an R software package. Molecular Ecology Resources. 2013;14: 652-663. doi:10.1111/1755-0998.12209
Author
Thierry Gosselin thierrygosselin@icloud.com
Examples
if (FALSE) { # \dontrun{
# The simplest form of the function:
hzar.data <- genometranslator::write_hzar(data = tidydata)
# Using genepop dataset, nancycats, from adegenet
# require(adegenet)
nancycats <- system.file("files/nancycats.gen", package = "adegenet")
# using genome_translator:
nanycats.hzar <- genometranslator::genome_translator(data = nancycats, output = "hzar")
# using the separate modules:
# tidy the genepop file then pipe the result in write_hzar
nanycats.hzar <- genometranslator::read_genepop(data = nancycats) %>%
genometranslator::write_hzar(data = .)
} # }
