Why Screen for Inherited Conditions?

Although individually uncommon, inherited diseases collectively account for approximately 20% of infant mortality and hospitalizations (PubMed: 22872815). Fulgent's Beacon Carrier Screening Tests go farther than any other: we do the deepest search possible for pathogenic carrier mutations for over 320 conditions.

Beacon can help to identify a couple's carrier status before or during pregnancy to enable informed decision-making and to better prepare for what lies ahead.

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Why Choose Beacon?

Fulgent Beacon Carrier screening tests are the most comprehensive ever offered.

  • Largest panel available, covering over 320 conditions
  • Next Generation Sequencing (NGS) of entire genes, not just hotspots
  • Deletion and duplication analysis
  • Fulgent’s signature customizability
  • 2-3 week turn-around-time and affordable prices

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Why Choose Fulgent?

Fulgent is accustomed to analyzing rare diseases and a leader in Next Generation Sequencing. Applying our expertise, we are capable of:

  • Over 99% detection of known mutations
  • Over 98% analytical detection for all 330+ genes
  • Detection by sequencing and by CNV deletion / duplication
  • Customizable Condition Screening

Conditions Tested

We test for 320+ autosomal-recessive and X-Linked genetic conditions, including:

  • Cystic Fibrosis - Beacon can detect more than 500 different mutations
  • Fragile X - Beacon also detects automatic AGG interruption, further refining your risk level
  • Duchenne Muscular Dystrophy - The most common form of muscular dystrophy affecting children
  • Hemoglobinopathies - Including alpha thalassemia, beta thalassemia, and sickle-cell disease
  • Spinal Muscular Atrophy (SMA) - Including enhanced SMA (2+0) screening to identify a silent carrier

Request Specimen Kits

Fulgent offers free specimen collection kits for physicians and genetic counselors within the continental United States.

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Quality

Our Lab is CLIA-certified and CAP accredited and surpasses the standards of diagnostic testing. All specimens are processed at our US laboratory. All data analysis is performed on private US server centers.


Fulgent Supports You

Our Learning Corner provides an approachable intro to the basics of genetics, inheritance patterns, and Beacon carrier screening, and even a risk calculator to use with your patients. We also offer post-test genetic counselling services.

Learning Center

Our live Chat feature can connect you with our team if you have about any questions of our tests. Hours of operation are from 8am PST - 6pm PST.