• Fix the one column matrices in dplyr::filter warning.
  • Fix the error when dplyr::select couldn’t find the column STRATA.
  • Open the parallel.core argument for some internal functions to help windows users with parallel processing problems in R. #188
  • Work around for .DynamicClusterCall pushed greavess #189
  • Fix issue #188 related to coverage in DArT 1row and 2rows format
  • works with R 4.3.4
  • Fix issue #186 related some particular DArT files
  • Fix issue #187 related to sexy_markers and VCF files
  • works with R 4.3.3
  • Updated DArT code that use COUNT files to check more for problematic markers usually stemming from merged projects
  • Bug fix using coverage and DArT data
  • Bug fix stemming from genalex files and genind conversion
  • Several bug fix while reading VCF from ipyrad
  • Additional checks during DArT file reading.
  • Bug fix with pcadapt, bayescan, genlight output thanks to @jcaccavo. Confusion between POP_ID and STRATA remained for some less used functions while the migration towards STRATA only inside radiator.
  • huge work on filter_ma that now incorporate Minor Allele Frequency (MAF), Minor Allele Count (MAC) and Minor Allele Depth (MAD).
  • bug fix when using some tidy function from GDS, the connection was not closing properly
  • work on genind, genlight, genepop, hierfstat, arlequin functions
  • updated the vignette
  • bug fix with reading VCF, the new update works with SeqArray (>= 1.36.0)
  • work on Tidy VCF.
  • bug fix when using arlequin output file
  • bug fix using DArT data
  • bug fix when using genepop file and genomic_converter
  • bug fix in genomic_converter when using genlight as input and PLINK as output file
  • More GATK VCF problems detections and warnings
  • updated to work with R 4.1.0
  • bug fix with some format during conversion when necessary genotype format wasn’t found
  • more safe results when importing VCF files with windows and parallel processing
  • bug fix using plink files and future
  • continue to test future backend and carrier
  • bug fix when using microsatellites as input and some specific output format
  • No longer using Travis CI and AppVeyor to test the package
  • R-CMD-check: now using GitHub actions and rhub that test on the 3 OS.
  • Taking advantage of future, furrr and carrier packages
  • PLINK files: fix a couple of bugs reading the tped
  • removed tidyr::gather and tidyr::spread dependencies (they are deprecated)
  • DArT data in 1-row format was not working properly with latest data.table melt function. Changed to tidyr::pivot_long.
  • updated radiator so that it work with latest release of SeqArray (v.1.28.1), that introduced breaking changes.
  • fineRADstructure rules have changed, I’m no longer doing gymnastic to make the population work with genomic_converter or write_fineradstructure, it’s not up to the user to make sure the pop id starts with a letter. Some codes might now be broken because of this.
  • read_plink and tidy_plink: new rules to get the best out of PLINK tped and bed files.
  • detect_microsatellites: new radiator function that detect microsatellites using GMATA.
  • 2 new output formats: genepopedit and rubias
  • 1 new detect function: detect_paralogs that copy the method described in McKinney et al. 2017. This function is the logical step to make available for users after detect_mixed_genomes, filter_hwe and sexy_markers.
  • sexy_markers: couple of bug fixed. More testing with the different genomic format.
  • There is still documentation and vignette to fix, but this is the release that will be submitted to CRAN
  • Major SeqArray and GDS integration
  • Imputation module was removed from radiator and now lives exclusively in package grur
  • filter_dart is deprecated. Please use filter_rad, the ONE function to rule them all;)
  • Worked on travis
  • pkgdown website
  • vignettes
  • better function doc
  • snp.ld: using missing data now works by chromosome/scaffold.
  • tidy_vcf, tidy_genomic_data and genomic_converter: works better with ipyrad vcf’s
  • tidy_vcf, tidy_genomic_data and genomic_converter: works better with freebayes and stacks vcf
  • tidy_vcf, tidy_genomic_data and genomic_converter: work without strata/pop grouping
  • snp_ld: new argument ld.threshold for long.distance linkage disequilibrium.
  • write_vcf: will now output ID as LOCUS_COL or LOCUS_(POS-1) if COL info is not provided.
  • tidy_vcf, tidy_genomic_data and genomic_converter: way faster with huge VCF
  • tidy_vcf and write_seqarray: work better with vcf generated by Stacks
  • write_ldna: new function that generates a LDna input file from a tidy data frame.
  • tidy_vcf, tidy_genomic_data and genomic_converter: way faster with huge VCF
  • write_fineradstructure: fix bug when data was from DArT
  • genomic_converter, tidy_genomic_data: bug fix when individuals are integers
  • fis_summary: arguments updated
  • filter_dart and filter_rad: can now opt out of HWE filtering.
  • filter_hwe: user can opt to see figures but skip filtering
  • working to make radiator work correctly with ggplot2 v.3.0.0
  • radiator ready for R 3.5.1 “Feather Spray” released on 2018/07/05
  • transferred write_gsi_sim from assigner to radiator
  • 2 write functions: write_snprelate and write_seqarray
  • when individuals in strata file/object and data don’t match, an error is generated
  • to reduce radiator dependencies, several packages were moved in the Suggests field.
  • filter_dart: lots of new stuff. More appropriate filter arguments:
    • filter.coverage is deprecated in favour of: filter.markers.coverage
    • filter.ind.missing.geno is deprecated in favour of: filter.markers.missing
    • erase.genotypes: new argument tailored to handle coverage for DArT counts data.
    • filter.individuals.missing: allows to blacklist sample early in the filtering pipeline.
  • New output file: stockr This output file format enables to run the data in the stockR package from Scott Fisher at CSIRO in Hobart.
  • New output file: related This output file format enables to run the data in the related R package, which is essantially the R version of COANCESTRY fortran program developed by Jinliang Wang.
  • New output file: fineRADstructure
  • Better VCF parsing
  • radiator is ready for stacks v.2 beta8
  • starting to re-introduce data.table to increase speed during melting or casting data frames
  • tidy_genomic_data and genomic_converter: bug fix and improvements.
  • write_snprelate and it’s associated output from genomic_converter is no longer available because of difficulties students are having in installing the package, it’s dependencies and/or using the output. The code remains available here, without support.
  • radiator::snp.ld: the module inside tidy_genomic_data and genomic_converter to minimize short linkage disequilibrium as a new option snp.ld = "middle". For locus with > 2 SNPs/read the option allows to select at random one SNP between the first and the last SNP on the read. If the locus as <= 2 SNPs on the read, the first one is selected. Note that for that last option, the numbers are reported. Thanks to Ido Bar for the idea.
  • tidy_dart and filter_dart:
    • big overhaul.
    • importing 1 and 2 row genotypes (called sometimes binary format) is easier and no longer require to prep the DArT file (the function parse DArT data with * at the beginning of certain lines).
    • filtering is easier and now interactive for those who want.
    • plots are generated automatically.
  • tidy_genomic_data and genomic_converter can now accept DArT data directly.
  • several typos where fix. Thanks to @IdoBar for this.
  • new function: run_bayescan to run BayeScan … with radiator
  • new separate write functions also included in genomic_converter: write_bayescan, write_pcadapt and write_hzar.
  • small mod
  • writting in specific folder
  • writting specific plot
  • Work on different functions to prep for official package launch
  • First commit