Genomic Unity® Exome Plus Analysis
Use
Genomic Unity® Exome Plus Analysis is a comprehensive diagnostic test designed to identify genetic variants that correlate with the patient’s phenotype. It analyzes both patient DNA and parental DNA (when available) for comprehensive insights. The test provides a single, unified clinical report replacing multiple tests, including whole exome sequencing (WES), chromosomal microarray (CMA), multiplex ligation-dependent probe amplification (MLPA), and more. It is recommended for cases where symptoms may be caused by a variety of genes or genetic mechanisms and when a specific diagnostic test is not available.
Special Instructions
Not provided.
Limitations
The sensitivity for mitochondrial large deletions and repeat expansions has not been determined. While the test covers a wide range of genetic variants, certain technical and interpretive constraints may affect the detection and analysis of specific variant types.
Methodology
NGS (WGS)
Biomarkers
Result Turnaround Time
4-6 weeks
Related Documents
For more information, please review the documents below
Specimen
Whole Blood
Volume
5ml
Minimum Volume
Not provided