Variant & sequence analysis
Analysis and interpretation support over variant and sequence data.
- Variant prioritisation and interpretation
- Sequence QC and anomaly detection
- Human review of material calls
Variant and sequence analysis where each call traces back to the evidence — for research and clinical genomics teams that need reproducibility.
Genomic analysis generates more data than any team can review by hand, and the interpretation is where the risk sits. A variant call that cannot be traced is a claim, not a finding.
Reproducibility is the currency of the field. If a result changes when the pipeline changes — with no record of why — it will not survive peer or clinical review.
Our view: provenance is part of the analysis, not a report bolted on afterwards. The pipeline, the model and the evidence are one record.
Analysis and interpretation support over variant and sequence data.
Pipelines designed so the same input yields the same, traceable output.
Every call tied to the reads, references and model decision behind it.
Evidence assembled to support classification and review.
We map the assay, reference genome and the clinical or research question.
We build the analysis into your pipeline and validate it against known results.
We prove reproducibility, document provenance and hand over the pipeline.
We will analyse a sample of your data and show how each call traces back to its evidence — before you commit to anything.
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