fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing

fast sample-swap and relatedness checks on BAMs/CRAMs/VCFs/GVCFs... "like damn that is one smart wine guy"

genetic variant expressions, annotation, and filtering for great good.

nim wrapper for htslib for parsing genomics data files

seqcover allows users to view coverage for hundreds of genes and dozens of samples