We offer the Variantyx Unity™ whole genome sequencing (WGS) test for diagnosis of rare inherited disorders. Patient samples are processed via our Genomic Intelligence® platform, using provided phenotype information to guide the analysis. Our board-certified medical geneticists consult with the ordering clinician or genetic counselor to review the analysis results and generate a signed clinical report.
1WGS analysis includes small sequence change, gross structural variant (CNV), short tandem repeat and mitochondrial genome sequencing analysis. Conducted on Illumina platform using Illumina TruSeq DNA PCR-Free Library Preparation Kit at 30X mean mappable coverage.
Our services are HIPAA and CLIA compliant, CAP accredited and fully insured. Payment by institutional billing or direct patient payment is accepted. Orders are subject to accepting test requisition and informed consent forms. Local taxes may apply.
To place an order, please fill out the form below. After your order is received, one of our clinical coordinators will get in touch to provide the informed consent and requisition forms and to coordinate sample collection and shipping. For help placing an order, please contact our clinical coordinators directly at firstname.lastname@example.org.