# --------------------------------------------
# CITATION file created with {cffr} R package
# See also: https://docs.ropensci.org/cffr/
# --------------------------------------------
 
cff-version: 1.2.0
message: 'To cite package "VarCon" in publications use:'
type: software
license: GPL-3.0-only
title: 'VarCon: VarCon: an R package for retrieving neighboring nucleotides of an
  SNV'
version: 1.20.0
doi: 10.32614/CRAN.package.VarCon
abstract: VarCon is an R package which converts the positional information from the
  annotation of an single nucleotide variation (SNV) (either referring to the coding
  sequence or the reference genomic sequence). It retrieves the genomic reference
  sequence around the position of the single nucleotide variation. To asses, whether
  the SNV could potentially influence binding of splicing regulatory proteins VarCon
  calcualtes the HEXplorer score as an estimation. Besides, VarCon additionally reports
  splice site strengths of splice sites within the retrieved genomic sequence and
  any changes due to the SNV.
authors:
- family-names: Ptok
  given-names: Johannes
  email: Johannes.Ptok@posteo.de
repository: https://bioc-release.r-universe.dev
commit: 6c2cd255c8c740049bc6fce14a85ace9f382e000
date-released: '2026-04-28'
contact:
- family-names: Ptok
  given-names: Johannes
  email: Johannes.Ptok@posteo.de