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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