A documented pipeline, from request to result
The HMP platform is open to research teams, laboratories and institutions. Each analysis follows a documented workflow: feasibility review, quote, sample reception, sequencing, quality control and interpretation.
Request
Choose an analysis in the catalogue and describe your project: objective, sample count, matrix, constraints and timeline. You receive a tracking reference immediately.
Review
The HMP team confirms feasibility, turnaround and the quote, then sends shipping and sample-preparation instructions.
Analysis
Samples are processed on HMP platforms. Extraction, library preparation, sequencing and quality metrics are recorded for every batch.
Interpretation
Results are annotated and interpreted, then delivered in your account with the methods, QC metrics and reproducibility information.
Quality controls
- Negative and positive controls in every sequencing run.
- Coverage, read quality, duplication and contamination thresholds reported with each sample.
- Reference genomes, pipeline versions and parameter sets recorded for reproducibility.
- Raw data retained according to the agreed retention period.
Who can request
- Academic and clinical research teams.
- Public and private laboratories.
- Biotech and pharmaceutical partners.
- Institutions requiring a documented service agreement.
Ready to start?
Submit a request in a few minutes. An HMP account is created for you after approval.