Dr Meriel McEntagart
Clinical Geneticist,
St George’s University Hospitals NHS Foundation Trust
Accelerate your throughput.
Ensure the highest standards.
Partner with Wellcome Sanger Institute-based, NHS-trained and HCPC-registered Clinical Scientists for complete NGS interpretation support, from intitial assessment through finalized reporting.
First Check
Rigorous variant classification following evidence-based clinical standards and current best practices.
Second Check
Second-expert validation ensuring classification accuracy and robust analytical integrity.
Final Report & Sign-Off
Comprehensive reports transforming genomic findings into clinical recommendations after thorough validation.
Our adaptable solutions align with regional clinical governance requirements. Contact us to discuss your objectives and confirm service accessibility in your area.
Get in touch7000+
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
Partners in your success.
Scale-ready and future-proof.
Manage your backlog
Scalable expert support to handle growing case volumes, with fast, reliable reporting.
Empower your team
Expert-led training in exome and genome analysis — from workflow guidance to clinical onboarding.
End-to-end genomic support
From sequencing data to clinical findings, we handle the pipeline so your team can focus on patient care.
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.”
