Services
Every genomics service, end to end — from a single Sanger read to whole-genome projects, medical genomics, NGS and expert bioinformatics, all with transparent pricing.
Not sure which service you need?
Tell us about your project and our team will recommend the right workflow and pricing.
Explore our services
Browse by category to find the right service for your research or clinical needs.
Genomic Services
End-to-end DNA/RNA extraction, library prep, sequencing and custom bioinformatics workflows.
Medical Genomics
Clinical-grade testing — exome, whole-genome, NIPT and microbiome — with clinician-ready reporting.
Next-Generation Sequencing (NGS)
High-throughput WGS, WES, RNA-Seq and metagenomics on Illumina, Nanopore and MGI platforms.
Bioinformatics Services
HPC-backed assembly, variant calling and RNA-Seq analysis delivering publication-ready results.
Other Services
Specialised and custom research support beyond our core sequencing and analysis catalogue.