Identify mutations and variants in solo or paired human whole genome sequencing data.

Characterise micro- or macrobiology composition using amplicon marker genes. 

Quantify gene expression across whole transcriptomes using bulk RNA-seq data.

Identify known and unknown viral sequences from shotgun or viral-enriched metagenomic data.

High-precision mapping of protein-DNA binding sites using CUT&RUN and CUT&Tag.

Assemble and analyse mitochondrial genomes from short-read sequencing data.