Tests
Single Gene Analysis
Chromosomal Microarrays (CMA)
CMA is the gold standard technology for analysis of CNVs (deletions and duplications) at chromosome level More informationPrecision Panels
A diagnostic test based on NGS of multiple genes associated with a disease, condition or phenotype
More informationWhole Exome Sequencing (WES)
A diagnostic test based on NGS of the complete coding region of all genes of the Human Genome. WES is the best option for non-specific genetic diagnosis More informationPanels by specialities
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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
More Information![Newborn Screening](https://www.igenomix.eu/wp-content/uploads/sites/25/2021/05/NBS-logo-web.png)
Newborn Screening
More InformationOptions according to your patient’s needs
Helping you in your clinical decision-making