Eurofins Biomnis Genetic Testing
Genetic Diagnostics with Clinical Training to Interpret Tests & Use the Technology
Eurofins Biomnis provides an exceptional level of service to clinicians who order Genetic Tests. Clinicians can choose from 3 levels of service when booking a test: For experienced clinicians, raw data may suffice but for less experienced professionals, result interpretation with or without training may be preferred. For clinical pathologists who want to learn more and get more involved in the interpretation of data, Eurofins Biomnis provide access to SeqOne, a secure bioinformatics platform.
What test do you require?
We offer single gene testing, fixed panels, customised panels, whole exome sequencing and whole genome sequencing.
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Single Gene |
A clear phenotype and strongly suspected single candidate gene |
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Gene Panel |
Phenotype suggests a group of genes are involved |
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Whole Exome Sequencing (WES) |
If genetics are suspected but the specific gene(s) are unknown, or when symptoms are unusual or affect multiple organ systems |
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Whole Genome Sequencing (WGS) |
Negative exomes with a strong family or clinical history: https://eurofinsireland.com/WGS-Testing |
We encourage clients to consider Whole Exome Sequencing (WES) because:
- WES sequences ~all of the coding regions of the human genome (containing more than 85% of pathogenic mutations)
- WES has a higher diagnostic yield than gene panels
- WES is more comprehensive than a gene panel
- It is time-saving for the clinician when the case is very complex
- We can re-interpret the whole exome data, should new genes or possible pathogenic variants arise later, without requiring a second sample from the patient
Genetic Tests by Medical Specialisms
Companion Diagnostics
Pharmacogenetics
The Eurofins Biomnis France Genetics Team
Genetic Testing Experience & Accreditation
Eurofins Biomnis France founded in 1897, has a long history of innovation. It was certified for Trisomy 21 in 1998, created a genetic finger-printing laboratory in 2004 and since 2008 has been adding technologies to detect oncology markers with NGS added in 2013.
Accredited ISO15189 for all NGS activities (including Whole Exome Sequencing) since 2019, we have built a sizable genetics team in Paris and Lyons, offering a wide array of tests: single gene; fixed panel; whole exome sequencing and genome sequencing.
Expert Genetic Speakers for Irish Genetic Events
From the French team, the following people can speak at healthcare events to share their genetic and clinical knowledge. If you are looking for a speaker, email: marketing@ctie.eurofinseu.com
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Dr. Laure Raymond is a laboratory geneticist and Head of the Genetics Division at Eurofins Biomnis, a leading provider of specialised laboratory medicine. Her academic background combined a PharmD and a research Master’s degree, followed by a residency in medical biology in Paris hospitals. For over fifteen years, she has been actively involved in the development and coordination of clinical diagnostic activities, particularly in constitutional genetics. Driven by her passion for innovation and her practical mindset, she ensures that the projects developed with her teams are implemented swiftly while maintaining a high standard of medical service. She works closely with academic and hospital partners to support their research and precision diagnostic projects. Among her recent initiatives is the extraction of pharmacogenetics information from exome sequencing data. Applied to patients with psychiatric disorders or kidney diseases, it enables a comprehensive genetic assessment, to personalize their care. |
French Genetic Test Guide
Search the French Test Guide for all other genetic tests:
Eurofins Biomnis international test guide dedicated to Genetics: Genetics test guide | Eurofins Biomnis
