| filterpos | Filter variants against known SNP dataset |
| filtervcf | Filter variants with user-specified quality criteria |
| gefreq | Frequency analysis at gene level |
| getref | Download reference gene annotation |
| LoadFiltering | To load and filter variants in batch mode |
| Patterning | Extract variants with user-specified variant pattern |
| Pos2Gene | Map sequencing variants to gene |
| pos2seq | Positions to sequencing calls |
| read.vcf | Read VCF file |
| subvcf | Subset of VCF data |
| vcfreq | Variant frequency of a varlist |
| VPA-package | Extract variants from VCF data with specified variant... |
| write.vcf | Write VCF object |
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