Where every gene tells a story

Genetics

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Genetics

Genetics at Unilabs

Our genetics services combine advanced technology, comprehensive testing capabilities and a network of experienced geneticists to support more precise, informed diagnostic decisions. From understanding the role of genetics in diagnostics to leveraging the benefits of technology and customisable panels, we work with healthcare professionals to enable better care across every stage of the patient pathway.

Our genetics activity & footprint

Our genetics services

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Reproductive Health

  • Prenatal Diagnosis

  • Infertility panels

  • Carrier Screening

  • Chromosomal analysis

  • NIPT


Medical areas and tests in-depth

Our portfolio of more than 4,000 tests are customisable to adapt to you and your patient’s unique needs.

Reproductive Health

Prenatal Diagnosis
Screening and diagnosis on prenatal samples (foetal cells or foetal cellfree DNA) can detect the presence of aneuploidies, monogenic diseases, or other genomic structural abnormalities, thus identifying high-risk pregnancies.

Infertility panels
Infertility tests can identify the genetic infertility cause and facilitate informed family planning that may include assisted reproductive technology, such as IVF.

Carrier Screening
Our WES-based carrier screening is designed to detect variants across diverse ethnic backgrounds, safeguarding against overlooked population-specific risks. This allows families to make informed decisions, prioritising the health of future generations during their planning process.

Chromosomal analysis
Karyotype analysis can detect structural (balanced rearrangements) and numerical (changes in sex chromosomes) abnormalities that can be the cause of reproductive disorders.

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Pathology

Leveraging our genetics database to enhance your diagnostics

Unilabs’ extended genetic database contributes to high-quality research, improved diagnostic accuracy, and helps inform personalised medicine. It supports you through:


10+ years of Data
Thousands of data sets that strengthen research and clinical interpretation.


Global coverage
Services provided in Europe and the Middle East.


Diverse & Unbiased insights
Genomic variants from multiple populations.

We leverage our international network of expert pathologists to best support your local needs by providing thorough slides interpretations, aiming for timely diagnosis, reliable assessments, and improved patient outcomes. With more than 350 pathology experts across Europe, one of the largest networks in the field, we can support you across a wide variety of medical specialties and subspecialities, providing you with fast and reliable diagnosis as well as second opinions for complex cases. Our extensive network is stepping up to help you face the challenge of the ever-higher demand for pathology services and the shortage of pathology professionals by embracing digital pathology.

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Genetics

Ensuring high quality standards, accreditations, certifications and external quality assessment

Our laboratory network reflects our commitment to quality and excellence in diagnostics, supported by extensive accreditations and certifications including ISO 15189, ISO 17025, ISO 9001, ISO 14001, and CLIA.


In addition to these accreditations, we participate in respected External Quality Assessment Programs such as Genomics Quality Assessment (GenQA), UK NEKAS, and The European Genetics Quality Network, among others. 


This comprehensive approach to quality assurance, combined with participation in these programmes, reinforces our adherence to established standards and provides confidence to our customers – physicians, patients, and health authorities – in our capability to deliver reliable results.