Sequencing
State-of-the-art Genetic Analysis Laboratory
GENOMA has developed one of the largest clinical genetic centers for screening and diagnostic tests in Europe, a high throughput Next-Generation Sequencing (NGS) laboratory.
Sequencing is the determination of the exact order of the base pairs in a segment of DNA. Genoma chose Next-Generation Sequencing (NGS) technology as it simultaneously sequences millions of DNA fragments for a fast an most comprehensive screening of your genes and genome. Next-Generation Sequencing (NGS) is one of the most advanced genetic analysis technologies available today.
Using an automated closed high throughput robotic system during the whole process, manual errors are avoided and consistency in the results ensured. Full traceability is guaranteed throughout the entire procedure.
Bioinformatics
Bioinformatics is an interdisciplinary field that develops methods and software tools for understanding biological data, combining computer science, statistics, mathematics, and engineering. INKARYO, our proprietary bioinformatic solutions for genetic analysis transforms the NGS data into the most accurate and comprehensive analysis of the genome.
Accurate
Reliable
Fast
Certifications
Genoma Swiss Biotechnology is certified ISO 13485
ISO 13485 is an internationally agreed standard that sets out the requirements for a quality management system specific to the medical devices industry. With this certification, Genoma Swiss Biotechnology confirms its compliance to the regulatory applications for safety and quality of medical devices developed.
What means a CE marked IVD product?
The letters “CE” are the abbreviation of French phrase “Conformité Européenne” (European Conformity). A CE marked product is a declaration that the product complies with the essential requirements of the relevant European health, safety and environmental protection legislations, in practice by many of the socalled Product Directives that contains the technical specifications established by several European agencies to which the products must conform.
The «In Vitro Diagnostic Medical Devices» Product Directives (98/79/EC) applies for Diagnostics.