Dr Meriel McEntagart
Clinical Geneticist,
St George’s University Hospitals NHS Foundation Trust
Expert genomic interpretation, delivered fast.
Discover our clinical interpretation services.
Our NHS-trained Clinical Scientists at the Wellcome Sanger Institute support your lab with NGS interpretation, from first check to report.
First Check
Expert-led variant classification grounded in current clinical best practices.
Second Check
Peer-review by a second expert to ensure robust validation and classification integrity.
Final Report & Sign-Off
Translation of genetic data into actionable insights following rigorous validation.
Our flexible services are built to comply with the established clinical frameworks within select regions.
Let's connect to discuss your specific needs and confirm our ability to support your lab in your country.
7000+
Complex
WES and WGS
cases analyzed
Customized support
for labs of all sizes
From startups to large diagnostic centers
Full spectrum genomic analysis
From targeted panels to exome and whole genome sequencing
HCPC-registered,
DipRCPath and PhD qualified scientists
100+
Years of combined experience in diagnostics and screening
Based out of the
Sanger
Institute
Expertise across key areas
Annual External Quality Assurance
for interpretation and reporting
Tailored for your success.
Designed for scale.
Take Control of Your Backlog
We provide scalable expert support to manage growing caseloads, ensuring fast, reliable reporting.
Upskill Your Team
Train your staff to master exome and genome analysis with expert guidance, workflow training, and clinical onboarding.
Full-Service Genomic Analysis
From sequencing data to clinical results, we manage it all, freeing your team for critical patient work.
Trusted by Leaders in Clinical Care.
“The team has demonstrated its diagnostic utility even in cases where the low levels of the variant could have led to a missed diagnosis. It provides reassurance to our clinical team that such patients will not be missed in the future.”
