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rank2map when a chromosome had only one site.hybridIndex when there are no data.hybridIndex.vcf2diem to write all sites into one file when chunk = 1L, allow minimum number of required genotyped individuals per site, and subset sampleNames.txt to ChosenInds only.changePolarity argument in importPolarized.resolveChosenInds.hybridIndex function that returns a numeric vector suitable for plotting.vcf2diem to optionally output site location in BED format.plotPolarized.markerAxis to avoid plotting multiple tick labels over one another.plotMarkerAxis to check the expected user input.variantSites function that selects sites with required number of homozygous genotypes in a subset of individuals.\(x) syntax.plotPolarized to unlist and unname the values in HI.vcf2diem to allow a user-defined minimum number of homozygous individuals, and to allow subsetting the conversion to ChosenInds.rank2mapChr internal function to be more efficient. It now uses the Inchworm algorithm by Stuart J.E. Baird.rank2map to allow also a data.frame in the inclucedSites argument.vcf2diem obligatory output of sample names.smoothPolarizedGenotypes to return a weighted mode, added corresponding internal functions truncatedLaplace and unbiasedWeightedStateChoice.CheckDiemFormat.rank2map and smoothPolarizedGenotypes.diem.diem when number of iterations reaches maxIterations. importPolarized to accept multiple files and a logical vector indicating which sites to import. The file processing is parallelised.plotDeFinetti and plotMarkerAxis.plotPolarized to show colored tick marks for individuals and to accept selected graphical parameters.vcf2diem when requireHomozygous = TRUE.ChosenSites argument in diem that allows to select sites for identifying a barrier to geneflow. Polarity is calculated for all sites, but only ChosenSites influence the likelihood in each EM iteration.vcf2diem for multiallelic markers where REF allele is rare.diem. As a consequence ModelOfDiagnostic is no longer exported.diem now requires ploidies for all individuals in the input files listed in the files argument.ploidy = FALSE in diem that assumes all individuals are diploid across all compartments. vcf2diem functionality to optionally require homozygous individuals for both most frequent alleles.vcf2diem so that markers without homozygous genotypes or markers with only one heterozygous genotype are removed as non-informative for genome polarisation.vcf2diem documentation.vcf2diem for multiallelic SNPs.vcf2diem to convert SNP in vcf format to diem genotypes.myotis vcf dataset with documentation.diem.plotPolarized.markerPolarity.importPolarized and plotPolarized._ or U.NEWS.md file to track changes to the package.README.md with quick start analysis instructions.ChosenInds to include all individuals to diem. Any scripts or data that you put into this service are public.
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