For hospitals, clinics, doctors & researchers
A laboratory partner who understands the work.
From everyday referrals to funded research programmes, DNA Labs Kenya collaborates with healthcare and academic institutions across the country — with responsive communication, clear scientific standards and flexible pricing.
Why partners choose us
- LOINC-coded, interoperable reports for EMR workflows
- ACMG/AMP-based variant classification with clinical commentary
- Chain-of-custody protocols for legal & immigration DNA testing
- ISO 9001:2015 quality management; ISO 15189 accreditation in progress
Collaboration streams
Built for how you work
Pick the track that fits — every partnership includes a named contact and agreed turnaround commitments.
Hospitals & clinics
Referral pathways with coordinated sample logistics, shared reporting and periodic case reviews. We integrate with your discharge and outpatient workflows so patient care keeps moving.
- Priority sample processing & pickup schedules
- Joint CME / education sessions for your teams
Doctors & specialists
Direct access to our scientists for complex cases — test selection, variant questions and result interpretation support, with reports written for clinical decision-making.
- Pre-test counseling resources for your patients
- Second-opinion variant review on request
Research institutions
Sanger sequencing, NGS panels, custom assays and biobank support — with project design input, agreed data formats and batch pricing for grant-funded programmes.
- Study-ready protocols & documentation
- Confidential handling of research data & samples
Students & academic projects
Discounted laboratory services for college, master's and PhD research projects. We support student researchers with proposal guidance, cost-effective batch testing and honest advice about what your budget can achieve.
- Special academic pricing & phased project plans
- Methodology letters for ethics & funding applications
Simple onboarding
From first conversation to first result
Tell us what you need
Referral volume, research scope or student project goals — a short call is enough to start.
Agree the pathway
We confirm test menu, logistics, pricing and turnaround commitments in writing.
Start collaborating
Named contact, coordinated collection and reporting that fits your workflow.
Methodology
Scientific standards you can cite
Testing is performed using validated molecular methods including Sanger sequencing and next-generation sequencing (NGS) platforms. Variant interpretation follows ACMG/AMP technical standards, and reports are LOINC-coded for interoperability.
Our quality management system follows ISO 9001:2015, we operate under KMLTTB-regulated practice, and ISO 15189 accreditation is in progress. We are transparent about this status and will update partners as it advances.
Reporting standards
- LOINC-coded results for EMR integration
- ACMG variant classification: pathogenic, likely pathogenic, VUS, likely benign, benign
- Clinical commentary with recommended next actions
- Agreed turnaround with status updates during processing
Let's build better answers together
Start a partnership conversation.
Tell us about your hospital, clinic, practice, institution or student project — we will respond with a clear proposal.