Analysis Services

You send raw reads or a count matrix. We return the differentially expressed genes, the pathways they sit in, and figures ready for your manuscript.

Single-cell data is easy to generate and easy to over-interpret. We do the quality control properly, annotate cells against reference atlases, and tell you which clusters are real.

Variant analysis built for African genomes — where reference bias, population structure and under-representation in annotation databases all matter.

Genomic surveillance analysis with turnaround measured in days, built for public health laboratories that need results while they still matter.

From amplicon reads or shotgun data to taxonomic profiles, diversity statistics and differential abundance results that survive review.

Methylation arrays, bisulfite sequencing, ChIP-Seq, ATAC-Seq and CUT&Tag — processed, tested and interpreted against the right background model.

Statistical support from protocol through to the methods section — and the sample size calculation done before recruitment, not after.

The data that answers your question may already exist. We find it, reprocess it consistently, and analyse it — at a fraction of the cost of generating your own.

Machine learning only earns its place when it beats a simple baseline. We test that first, and we tell you when it does not.