devSEEK® Triome Sequence Analysis for Neurodevelopmental Disorders

Next Generation Sequencing panel focused on genes implicated in Developmental Delay, Intellectual Disability and Autism Spectrum Disorders

The devSEEK® Triome™ panel is designed to provide the most complete picture. It employs powerful trio analysis, by fully sequencing the parent’s samples along with the patient, to enable extensive genetic analysis and clinical interpretation of an expanded selection of genes (over 1,100) associated with developmental delay, and intellectual disability, and many additional genes that have recently been associated with autism spectrum disorder.

Autism spectrum disorders, developmental delay, and intellectual disability are diverse neurodevelopmental disorders. Multiple lines of evidence support the strong role of genetics in the etiology of these disorders. Courtagen’s Next Generation Sequencing Panel enables the rapid analysis of genes most commonly associated with genetic syndromes as well as nonsyndromic forms of these disorders.Obtaining genetic test results helps determine whether a known etiology is present. A definitive diagnosis facilitates appropriate medical, developmental, educational and community support interventions to optimize child and family well-being.

Indications for Testing

Primary Indications
Secondary Indications (examples)
Autism spectrum disorder
Short Stature
Developmental delay
Intellectual disability
Dysmorphic features
Cognitive Impairment
Brain malformations
Hearing impairment
Visual impairment

Muscular control: e.g. hypotonia,
hypertonia, tremors, hyperreflexia, atrophy
Failure to thrive

Product Information Sheet

devSEEK® Triome Sequence Analysis for Neurodevelopment Disorders

devSEEK® Triome Panel Gene List

Methylation SNP Analysis for devSEEK & devACT Panels

Methylation SNP Analysis SNP List for devSEEK Triome, devSEEK, devACT & theraSEEK

Courtagen's Unmatched Customer Support

Turn Around Time: 4-6 weeks. Results are delivered in weeks, not months.

Saliva Sample: DNA for sequencing is reliably extracted from a single saliva sample. No blood draw or muscle biopsy required. (Whole blood and tissue are accepted, as requested.)

Insurance Assistance: Courtagen works with patients, physicians, and insurance carriers to pre-approve each test. Courtagen will bill the insurance company, and is willing to handle an appeal process as needed.

Courtagen Care Financial Assistance Program: Provides financial assistance to patients based on demonstrated financial need. A qualified applicant may be asked to contribute between $0 and a maximum cost sharing of $200 depending on determination of financial need.

Online Portal: A secure physician online portal is available for ordering genetic tests and accessing patient reports when completed.

Genetic Counselors: Available to address physician’s questions regarding Courtagen test results. Contact us at

Clinical Experience: Courtagen’s Medical Director, Laboratory Director, and variant science team have over 25 years of experience in the treatment and genetic interpretation of neurological and metabolic disorders.

Reports: Utilizing Courtagen’s customized Ziphyr® informatics pipeline and thorough clinical evaluation, each report is provided in a concise format with interpretation and recommendations for consideration.

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