genetic testing doesn’t need to be complicated-let us help

Our goal is to enhance access to the most advanced genetic diagnostic services. Explore our tests and resources below to learn about the various ways we support providers and patients through every step of the genetic testing process.


Genetic Tests For Neurodevelopmental Disorders

FirstStepDx PLUS Chromosomal Microarray

Detect deletions and duplications (copy number variants) across the genome.

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Fragile X Syndrome Testing

Quantifies the CGG trinucleotide repeat in the FMR1 gene.

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NextStepDx PLUS Whole Exome Sequencing

Analyzes all protein-coding regions of over 20,000 genes in the exome.

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EpiPanelDx PLUS Genetic Testing

Analyzes 244 genes associated with infantile spasms, epilepsy, or encephalopathy.

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Mitochondrial DNA Testing

Sequencing and deletion analysis of all 37 genes of the mitochondrial genome.

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Genetic Test For Neuromuscular Disorders

FSHD1 Testing

FSHD1 high resolution coverage of the D4Z4 repeat regions on chromsome 4 & 10 utilizing optical genome mapping.

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Genetic Test For Drug Response

Pharmacogenetics Panel

ldentifies variants known to influence medication metabolism.

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