From raw reads to clinical-grade insight
Bioinformatics
Validated, reproducible pipelines that turn sequencing output into decisions. We build the computational backbone that makes precision medicine operational — versioned, auditable, and fast enough for clinical timelines.
Delivered AI-native — lean, fast, compliant and cost-effective. No AI coating, no legacy bloat, no year-long rollouts.
Capabilities
What we deliver
NGS pipeline engineering (WGS, WES, RNA-seq, methylation)
Variant calling, annotation and prioritisation at scale
Workflow orchestration with Nextflow and Snakemake
Clinical reporting interfaces co-designed with pathologists
Continuous validation against reference standards
Cloud-native, cost-optimised compute architectures
Our targets
The bar we hold ourselves to on every engagement — and report against, honestly.
70%
faster turnaround from sample to report
100%
pipeline reproducibility and audit trails
40%
lower compute cost per genome
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