BRINGING GENOMICS
TO PRECISION MEDICINE
Genetic diseases are numerous and global, affecting 6-8% of the population. An accurate genetic diagnosis is the best solution for your patient.
Tests
Single gene analysis
Diagnostic testing for a specific genetic condition associated with variants in a particular gene or genomic region.
Chromosomal microarrays (CMA)
Analysis of deletions and duplications at the chromosome levelusing CMA, the gold standard technology for copy number variation (CNV) analysis.
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Precision panels
A diagnostic test using next generation sequencing (NGS) of multiple genes associated with a condition or phenotype.
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Whole exome sequencing (WES)
A diagnostic test using next generation sequencing (NGS) of the protein coding regions of the genome - the best option for a non-specific clinical presentation.
Contact usPanels by specialities
Newborn Screening
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Prenatal
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Oncology
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Rare Disease
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Neurology
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Skeletal
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Cardiology
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Ophthalmology
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Connective
Tissue
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Gastroenterology
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Dermatology
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Endocrinology
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Hematology
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Metabolic
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Immunology
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Nephrology
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Pulmonology
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Ear, Nose, Throat
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Rheumatology
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Preventive Medicine
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Alyssa Armsby
Genetic Counsellor
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Lizzie Verdon
Genetic Counsellor
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Dr Roy Pascal Naja
Laboratory Director
BROCHURE
Options according to your patient’s needs
Helping you in your clinical decision-making
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