GTAC at MGI provides the technical sequencing services for these established assays in compliance with CLIA certification and CAP accreditation requirements. This ensures your test results will meet industry standards for clinical laboratory testing. These are directly orderable through our colleagues at
Targeted hybridization capture of tumor-derived genomic DNA coupled with next-generation sequencing (NGS). This approach enables deep, comprehensive coverage of all coding exons and key introns of ordered genes, and allows assessment of the molecular complexity of each DNA specimen, minimizing sampling bias even in cases of low DNA mass or quality.
What variations detection is available?
A targeted sequencing assay for 40 genes and gene hotspots that are recurrently mutated in acute myeloid leukemia and myelodysplastic syndrome using UMI-based targeted sequencing with the Agilent HaloplexHS.
Exome sequencing of a tumor/normal sample pair with automated tumor-associated SNV and small coding indel variant detection.GTAC