Our Inherited Disease Panel tests over 300 genes applicable to over 700 unique inherited diseases, including neuromuscular, cardiovascular, developmental, and metabolic diseases. This screening test can be used for preconception testing of prospective parents to screen for potential overlapping genetic disorders as well as diagnosis of inherited conditions.

Establish your genetic risk of hereditary cancers. We offer a cancer panel test which will look for a total of 92 mutations associated with hereditary cancers. The genetic predisposition test for cancer is a powerful tool that can help you reduce your risks or undertake measures that will help you detect any cancers as early as possible.

This Specialized Test Panel includes screening of BRCA1 and BRCA2 genes. Mutations in BRCA1 and BRCA2 increase the risk of developing female breast and ovarian cancers as well as other cancers including pancreatic cancer and endometrial cancer.

Cystic fibrosis is a condition which mainly affects the lungs and pancreas, but can affect other parts of the body, including the liver, nose and sinuses, reproductive organs, and sweat glands. Our Cystic Fibrosis testing is performed using massive parallel sequencing (next generation sequencing) which allows for the analysis of exons, intron-exon boundaries, and UTRs that contain common mutations in the CFTR gene. This methodology with sequence analysis of all exons, intron/ exon borders, promoter regions, and specific intronic regions detects more than 98% of CFTR mutations.
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