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Science Lab

Clinical Genomics

Empowering families with the science of genomics

AGTC Clinical Genomics Solutions place families at the heart of precision medicine. By unlocking insights hidden in our DNA, we enable earlier and more accurate diagnoses, minimize treatment risks, and ensure optimal outcomes for every individual. Our advanced genetic testing empowers healthcare professionals to make informed decisions—predicting disease risks, tailoring treatments, and guiding care with confidence. Together, we bring the science of genomics into everyday healthcare, promoting healthier futures for patients and families alike.

See Diagnostics In a New Way

Obtain valuable insights that can enhance diagnosis, prognosis, and the overall quality of patient care.

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NovaDx™

Clinical Whole Genome Sequencing

For individuals or families wanting to understand inherited genetic conditions early

  • Preventive care, family planning, and carrier screening.
  • Diagnosing complex or rare diseases.
  • Rapid diagnosis in critical care settings (e.g., NICU/PICU).
Sample types

Saliva, Blood or Buccal Swab

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InsightDx™

Clinical Exome Sequencing

For patients with symptoms of genetic disorders

  • Preventive care and family planning.
  • Diagnosing rare or complex genetic disorders, especially when WGS is unnecessary or unavailable.
Sample types

Saliva, Blood or Buccal Swab

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HorizonDx™

Comprehensive Carrier Screening

For couples pursuing family planning and preventive genetic screening

  • Preconception and prenatal screening.
  • Testing before IVF or sperm/oocyte donation.
Sample types

Saliva, Blood or Buccal Swab

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OrigenDx™

Comprehensive Newborn Screening

New parents seeking reassurance about their baby’s genetic health

  • Early diagnosis of metabolic, amino acid, fatty acid, and endocrine disorders, among others.
  • Offers early detection and intervention, reducing the risk of permanent health damage with an accuracy rate of over 99%.
Sample types

Saliva, Blood or Buccal Swab

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OdysseyDx™

Rare Disease Solutions

For patients and families seeking answers to rare genetic disorders.

  • Diagnosing genetic causes of rare diseases.
  • Reduces the diagnostic odyssey by offering quick, accurate results using next-generation sequencing.

     
Sample types

Saliva, Blood or Buccal Swab

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PharmPGx™

Comprehensive Pharmacogenomics Test

For patients who want safer, more effective medications, and for healthcare providers seeking to personalize treatment.

  • Tailors drug treatments based on genetic profiles.
  • Reduces the risk of medication side effects.
  • Enhances the efficacy of prescribed medications.
Sample types

Saliva, Blood or Buccal Swab

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ContinuumDx™

Polygenic Disease Risks Prediction

For individuals who want to understand their genetic health risks and take proactive steps for prevention and early care.

  • Identifies genetic risk factors for common diseases.
  • Helps implement early lifestyle modifications.
  • Predicts long-term health risks to support preventive care.
Sample types

Saliva, Blood or Buccal Swab

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HLA-Dx™

HLA-Typing for Organ Transplant

For transplant patients, families, and healthcare providers seeking optimal donor-recipient compatibility.

  • Increases organ transplant success.
  • Reduces the risk of rejection.
  • Essential for organ transplant planning.
     
Sample types

Blood

Genomics for Families and Newborns

Comprehensive carrier screening, newborn health insights, and disease risk prediction to guide early intervention. Enable personalised care, informed family planning, and lifelong health management with advanced genomic testing.

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