MOLECULAR DIAGNOSTICS

What we offer

Unilabs has a broad range of experience in providing services within Molecular Diagnostics. Examples include – but are not limited to:

• Cross-functional collaboration between our high level experts in Lausanne and the GCP (Good clinical practice) team in Copenhagen
• Services within research of mutations associated to genetic diseases or syndromes, pharmacogenetics, oncogenetics, and personalized treatments
• High-throughput DNA sequencing by NGS technology provides a high level of detection sensitivity and confidence
• Flexibility in the variety of samples types (fresh, frozen, FFPE, fine needle aspirates (FNA), smears, etc)
• Simultaneous screening of multiple genomic aberrations like single nucleotide variants (SNPs), insertions/deletions, copy number variations and gene fusions
• Expertise in cell-free circulating DNA analysis (NIPT and liquid biopsy)
• Regulatory consultancy in relation to method validation
• Six geneticists, two medical geneticists, two onco-haematologists, and teams of highly specialised technicians
• Equipped with the latest technology for molecular diagnostics in Genetics and Cytogenetics (NGS, CGH-array, Sanger-sequencing, fragment analysis by capillary electrophoresis, real time PCR)
• Easy transfer of projects via our dedicated project manager between centres of excellence, with a wide service offerings, including immunoassays, molecular diagnostics, histopathology and medical imaging
• Management of centralised and de-centralised Companion Diagnostic (CDx) testing and global, customised logistics
• Customisation of every project – no matter the number of patients. This ensures you get exactly what is required for the project without unnecessary expense