NSG Testing

Next-Generation Sequencing (NGS) allows for highly detailed analysis of a patient’s genetic profile, uncovering variations linked to disease predisposition, drug metabolism, and hereditary conditions.

Metabolic
Identifies genetic mutations linked to enzyme deficiencies and inherited metabolic disorders, often critical in pediatric and rare disease diagnostics.

Hereditary Neurological Disorders Risk
Detects genetic factors contributing to neurological conditions such as epilepsy, dementia, and movement disorders.

Pulmonary
Analyzes genetic risk factors associated with chronic respiratory conditions, including COPD, asthma, and fibrosis.

CGX (Cancer Genomics)

Evaluates inherited cancer risks (e.g., BRCA1/2, Lynch syndrome) to guide prevention, surveillance, and treatment strategies.

Thyroid
Screens for variants affecting thyroid hormone production, autoimmune thyroid disease, and thyroid cancer predisposition.

Primary Immunodeficiency
Explores immune-related genetic markers, helping diagnose immunodeficiencies, autoimmune disorders, and hypersensitivities.

3380 Fairlane Farms Rd, Wellington, FL 33414, USA

We 're honored you've trusted ASL Laboratories with your trusting needs. Our team is committed to delivering accurate, timely genetic and diagnostic results with compassionate, concierge-style service. By choosing ASL, you're partnering with a laboratory that values precision, privacy and personalized support-helping you and your patients make informed decisions with confidence.