Genomic Testing | Fulgent Genetics

Exome Testing

Clinical Exome Sequencing and Whole Exome Sequencing help fill the gaps for patients whose needs go beyond preset and custom panel options. These are patient-centric, phenotype-driven analyses designed to examine coding regions and splice junctions for thousands of genes. Reports will only include the variants that are of plausible clinical relevance to your patient.

A woman is sitting in a lab with a pipette and test tube in hand.

Exome Sequencing Options

Clinical Exome Sequencing

Clinical Exome Sequencing tests over 4,500 genes known to be associated with inherited conditions. This option is ideal for patients with a clinical presentation indicative of a genetic syndrome not specific enough to point to a single condition. This test uses our custom-designed capture set, which is continuously improved and revalidated to cover the most clinically relevant genes and variants.

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Whole Exome Sequencing

Whole Exome Sequencing tests over 20,000 genes throughout the human genome. This option is ideal for patients for whom previous focused testing has been negative or those who have a complex or very rare combination of phenotypes that are not suggestive of any recognizable syndrome.

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What to Expect

Standard coverage is at least 96% at 20x with del-dup analysis
You may elect to opt out of the return of uncertain results (VUS)
Turnaround time is 5 - 7 weeks
Patients may receive medically actionable secondary/incidental findings (following ACMG guidelines)
STAT testing is available. Please contact the lab if you have a medical need for rush testing
Duo and Trio analysis of the patient's biological relatives is available at no extra cost

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We are available through phone, web chat, and email to assist with your orders and questions.

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Request a test kit

Fulgent offers free specimen collection kits for healthcare providers within the domestic United States.

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