| %variant_in% | Match variants by position and allele |
| %variant_in%-method | Match variants by position and allele |
| annotateWithControlDepth | Annotate Case with Control Depth |
| calculateConcordanceMatrix | Variant Concordance |
| calculateVariantConcordance | Variant Concordance |
| callGenotypes | Call Genotypes |
| callGenotypes-method | Call Genotypes |
| CallGenotypesParam | Call Genotypes |
| callSampleSpecificVariants | Call Sample-Specific Variants |
| callSampleSpecificVariants-method | Call Sample-Specific Variants |
| callVariantConcordance | Variant Concordance |
| callVariants | Call Variants |
| callVariants-method | Call Variants |
| callWildtype | Calling Wildtype |
| coverage_H1993 | Vignette Data |
| coverage_H2073 | Vignette Data |
| DepthFETFilter | Variant Filter Constructors |
| extractCoverageForPositions | Get Coverage at Positions |
| genome_p53 | Vignette Data |
| matchVariants | Match variants by position and allele |
| MaxControlFreqFilter | Variant Filter Constructors |
| minCallableCoverage | Calling Wildtype |
| MinTotalDepthFilter | Variant Filter Constructors |
| p53 | Vignette Data |
| pileupVariants | Nucleotide pileup from alignments |
| postFilterVariants | Post-filtering of Variants |
| qaVariants | QA Filtering of Variants |
| SampleSpecificVariantFilters | Call Sample-Specific Variants |
| SetdiffVariantsFilter | Variant Filter Constructors |
| tallies_H1993 | Vignette Data |
| tallies_H2073 | Vignette Data |
| tallyVariants | Tally the positions in a BAM file |
| tallyVariants-method | Tally the positions in a BAM file |
| TallyVariantsParam | Tally the positions in a BAM file |
| VariantCallingFilters | Call Variants |
| variantGR2Vcf | Create a VCF for some variants |
| VariantPostFilters | Post-filtering of Variants |
| VariantQAFilters | QA Filtering of Variants |
| VariantTallyParam | Tally the positions in a BAM file |