Founded in 2006, Amplexa Genetics is one of the longest-established private genetic laboratories worldwide, certified under ISO 15189. Our mission is to deliver genetic insights that empower informed decision-making. Whether you are an individual or a healthcare professional, our testing and research support you in making choices—from family planning to selecting the most appropriate treatment options for your patients.
- RAPID TURNAROUND WITH CONSISTENT QUALITY We deliver results quickly while maintaining the highest standards of clinical accuracy and reliability.
- AGILE AND ADAPTABLE APPROACH Our team is highly flexible, able to adjust swiftly to changing requirements and project scopes.
- PROACTIVE AND PERSONALIZED CLIENT ENGAGEMENT We prioritize strong, ongoing communication with our clients, ensuring responsiveness and tailored support throughout every stage of the collaboration.
- EXPERT OVERSIGHT Our experienced clinical team ensures that speed never comes at the expense of accuracy or compliance.
- REGULATORY CONFIDENCE Compliance with all relevant clinical and industry regulations, even on accelerated timelines.

SOLUTIONS FOR DOCTORS & PATIENTS

FERTILITY
Every fertility journey is different, and therefore the help that patients need is different. We want to help you offer the best treatment for your patients.

CLINICAL
One of the main challenges of current genetic medicine is supporting clinical diagnosis and providing preventive health care actions. Amplexa Genetics develops comprehensive clinical genetic tests.

NEUROLOGY
We offer the relevant test for patients suffering from epilepsy, intellectual disability, autism spectrum disorder with or without epilepsy.
SOLUTIONS FOR RESEARCH & TECHNICAL SERVICES

TECHNICAL SERVICES
We offer a variety of comprehensive, technical sequencing solutions, that combine science and information technology with our highly adaptable bioinformatics service.

RESEARCH & DEVELOPMENT
We are committed to advancing the field of genetic research by developing and refining sequencing-based methodologies.

BIOINFORMATICS
We can help you with everything from experimental design, the actual sequencing, data analysis, interpretation, as well as the production of publishable figures for the script or presentation.
AMPLEXA PUBLICATIONS
Find our publications here:
Applying cellular fixation and cell-type isolation for single-cell sequencing
Amplexa has supported Prof. Ditte C. Andersens-group in applying and validating a novel technique for cell isolation for single-cell sequencing that allows the samples to be stored at -80 degrees for a prolonged period before further single-cell library preparation.
Incorporating epilepsy genetics into clinical practice: a 360° evaluation
We evaluated a new epilepsy genetic diagnostic and counseling service covering a UK population of 3.5 million. We calculated diagnostic yield, estimated clinical impact, and surveyed referring clinicians and families. We costed alternative investigational pathways for neonatal onset epilepsy.
Importance of size of gene panels in diagnostics of children with epilepsy
Amplexa Genetics has in collaboration with three German laboratories; The Center for Human Genetics and Laboratory Diagnostics, CEGAT and Medical Genetics Center, has approved and published the article "Next Generation Sequencing in Pediatric Epilepsy Using Customized Panels: Size Matters".
