# ------------------------------------------------
# CITATION.cff file created with {cffr} R package
# See also: https://docs.ropensci.org/cffr/
# ------------------------------------------------
 
cff-version: 1.2.0
message: 'To cite package "VCFArrow" in publications use:'
type: software
license: MIT
title: 'VCFArrow: Fast and Memory-Efficient Manipulation and Conversion of VCF Files'
version: 0.9.0
abstract: Reads Variant Call Format (VCF) files into an S4 object whose genotypes
  are stored on disk as an 'Apache Arrow' dataset and loaded lazily, allowing large
  datasets to be processed with little memory. Provides functions to filter variants
  and samples, subset and merge datasets, compute summary statistics and diagnostic
  plots, write VCF files, and convert data to input formats of population genetic
  and phylogenetic software such as 'STRUCTURE', 'ADMIXTURE', 'PLINK', 'EIGENSTRAT',
  'Arlequin', 'GENEPOP', 'BayeScan', 'TreeMix', 'SNAPP' and 'adegenet'.
authors:
- family-names: Hrbek
  given-names: Tomas
  email: hrbek@evoamazon.net
  orcid: https://orcid.org/0000-0003-3239-7068
repository: https://cran.r-universe.dev
repository-code: https://github.com/legalLab/VCFArrow
commit: f11404c41aadaedfe434c7c8582719203849669a
url: https://legallab.github.io/VCFArrow/
date-released: '2026-10-16'
contact:
- family-names: Hrbek
  given-names: Tomas
  email: hrbek@evoamazon.net
  orcid: https://orcid.org/0000-0003-3239-7068