Fulgent offers rapid and accurate testing of specific mutations using the most optimal sequencing methodology. Detection status is reported in an informative and concise report.
Detection: Single nucleotide variants, small deletions and duplications, copy number variants
Methods: Sanger, qPCR, MLPA
Turnaround Time: 2-3 weeks
Complimentary familial known mutation tests are available for patients tested at Fulgent. Free carrier status detection is offered for clinically significant VUS(es) in both parents. Please contact our laboratory for additional information and limitations.
Fulgent also provides an assortment of specialized tests designed to detect specific genomic alterations that are beyond the capabilities of NGS. We are continuously developing new tests to meet your patients’ needs. Please reach out to our team to request additional assays.