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Medical Genetics

Medical Genetics

Our deep expertise in Medical Genetics and our high-quality genetic testing enables accurate diagnosis of genetic conditions across all medical specialties. ​

Supporting Pharmaceutical companies with genomic insights

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Unilabs Genetics provides high quality genomic services

At Unilabs Genetics we partner with pharmaceutical companies and CROs to support clinical studies with a comprehensive suite of genetic testing methodologies, tailored to the specific demands of each study protocol.

 

With extensive experience supporting clinical studies and research in rare diseases and oncology, our solutions are built to meet the demanding scientific and clinical requirements of modern precision medicine.

 

Our expert team — including clinical geneticists, quality and regulatory specialists, and dedicated project managers — ensures seamless, efficient operations that align with rigorous compliance standards.

 

Backed by a diverse biodatabase built over 15 years and drawn from representative populations across three continents (Europe, the Middle East and South America), we are uniquely positioned to deliver insights into both established and novel biomarkers.

Our Pharmaceutical partner services include:

  • Early stage biomarker discovery projects  
  • Evaluation and recruitment of patient cohorts for clinical trials  
  • Identification and stratification of patients for targeted treatment 
  • Genomics services for research and drug development 
  • Pharmacogenomic testing 

Sequencing Services for Research

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DNA Sequencing

Using the latest NGS technology and equipment Illumina NovaSeq6000, we make sequencing available to public and private academic and research institutes. 

 

Every project is managed by an expert team and customized according to our client´s requirements.  

 

This includes flexibility in options for: 

  • Sample type (blood, buccal swab, extracted DNA),  
  • Raw sequencing data output format (BAM, fastq)  
  • Bioinformatics analysis (vcf, annotation of SNVs, indels and CNVs) 

We can analyse a custom panel of genes, the entire exome or human genome. 

For large batch projects, we can also accommodate specific sequencing parameter requirements. 

 

Please contact us at genetics.info@unilabs.com to discuss a tailored solution to your project.  

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