- Use updated
R CMD checkCI/CD action.
- Add
methodargument toin.regionfunction
- Update changelog to Markdown
NEWS.mdformat - Use updated
renvGitHub action forR CMD check - Rename internal helper function
parse.vcf.header()toprep.vcf.header()to avoid naming conflict with base Rparse()S3 method.
- Replace outdated
autostartinfreadwithskip. - Fix cross-reference format in manual
- Update GitHub links
- Add LICENSE.md to repository
- Update DESCRIPTION to include URL and BugReports links
- Update CI/CD action
- Remove unnecessary package manual file
- Add vcf2bedpe module to convert structural variant calls obtained from Manta, GRIDSS and Delly v0.7.8
- forced vcf2bed not to print genomic coordinates in R scientific notation for interoperability with other processors
- Updated support for tabix version >1.1. tabix deprecated option -B is now replaced with -R
- fixed incorrect ordering of chromosome table returned by get.chr.length() - [rolled back]
- Added rmarkdown in Suggests section
- Parameterised test.region.similarity() with gaps.file and repeats.file to support custom files
- Exposed utility function bed2index() via NAMESPACE to support its direct usage
- Fixed bug when bedtools 'coverage' output is post-processed in bedr
- Fixed is.valid.seq() to comply with inputs and outputs as described in docs
- Standardised function name; renamed snm() to bedr.snm.region()
- Listed SystemRequirements to the package metadata
- Added support for Human hg38 genome assembly
- Fixed compatibility with data.table >= v1.9.6 for data.table::fread() call
- Fixed sort --version command as Solaris does not support --version which is GNU specific
- Initial release