FOCUSED & COMPREHENSIVE
Hereditary Cancer Testing

Panel Coverage

99.9%

at 50x Guaranteed

Deletion &
Duplication

≥ 1 exon resolution

Turnaround
Time

2-3 weeks

Customizable

Add additional
cancer genes or
panels at no charge

within 3 months

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Highlights of
Coverage and Analysis


  • > 99% coverage for coding sequences (50x or greater)

  • Deletion and duplication analysis with single exon resolution for all genes

  • BRCA2: Portuguese Founder Mutation

  • MSH2: Boland Inversion (exon 1-7 inversion)

  • PTEN: Promoter region

  • TP53: Promoter region

  • CDKN2A: p14ARF and p16 protein products

  • PMS2: Analysis includes exons 1-5 and 12-15

  • TERT: Promoter region

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Focus

Fulgent Focus Cancer Panels target 29 genes associated with high/moderate risk for hereditary cancer syndromes and established clinical management guidelines for disease-causing variants. These panels provide the most optimal balance between detection of pathogenic cancer susceptibility mutations, and minimizing the number of reported variants of unknown clinical significance.

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Comprehensive

Fulgent Comprehensive Cancer Panels cover 123 genes associated with potential risk for hereditary cancer syndromes. These panels include well-established cancer-related genes as well as candidate genes with newly discovered association with cancer, but may have reduced or unclear risk. Hereditary cancer syndromes with complex presentations may benefit from more comprehensive testing. Fulgent Comprehensive Cancer Panels maximize the chance of identifying disease-causing variants and provide an extensive review of potential cancer risks from additional candidate genes.

Customize for your Patient

Customize patient care by adding or removing any of our 123 cancer genes to suit your patient's condition and clinical management. Take advantage of our no additional charge re-requisition process to expand the diagnostic quest to any other gene in the cancer tests.

Specifications

Panel Coverage: 99.9% at 50x Guaranteed
Deletion / Duplication: ≥ 1 exon
Sequencing Methods: NGS
Orthogonal Methods: Sanger, qPCR, MLPA
Turnaround Time: 2-3 weeks