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The Oncomine Precision Assay on the Ion Torrent Genexus System is a next-generation genomic profiling solution that can allow every laboratory to deliver a genomic profile with a one-day, hands-free workflow.†
The Oncomine Precision Assay on the Ion Torrent Genexus System is a next-generation solution for genomic profiling that’s accessible for laboratories of all sizes. Now labs can employ a hands-off workflow to detect key biomarkers such as EGFR, ALK, BRAF, ROS1, NTRK, RET, or ERBB2 from formalin-fixed paraffin-embedded (FFPE) tissue or liquid biopsy specimens in one day.
Featuring the most prevalent and potentially relevant cancer driver variants across 50 genes, including potentially important resistance driving variants, this assay is ideal for fast genomic profiling in clinical cancer research.
Some NGS send-out labs have test failure rates of 20% due to their high input requirement. At that rate, one out of every five samples submitted will not pass due to lack of tissue, and many more are never submitted for testing at all.
Not with Oncomine Solutions.
You can experience a sequencing success rate of over 95% with Oncomine assays, because we only require 10 ng of nucleic acid input. That means you can get an NGS result for most of the precious samples you have.
In the drive to profile every important cancer sample, the tissue is still an issue, especially in some types of cancer such as non-small cell lung cancer (NSCLC). The Oncomine Precision Assay can deliver results from FFPE tissue as well as liquid biopsy if tissue is not available and can also be used for follow up to monitor the cancer profile development
There are a number of known and recurrent fusion isoforms that constitute a majority of the fusions detected. Having specific designs for these isoforms is important to maximize detection, even in challenging situations when sample input or transcript levels are low.
The optimized, synced design of the Oncomine Precision Assay enables comprehensive, sensitive fusion detection (including novel fusions in select driver genes) at low transcript or input levels.
Sample | Range | Variant type | # of variants per sample | # of sample replicates | Sensitivity | PPV |
Internal FFPE Control | 4.8% + 2.3% SD AF* | SNV | 67 | 32 | 99.6% | 99.6% |
INDEL | 4 | 32 | 100% | 100% | ||
Horizon Structural Multiplex FFPE Reference Standard | 3.5% to 17% AF* | SNV/INDEL | 15 | 32 | 100% | 100% |
4.5 copies | CNV | 1 | 32 | 93.8% | 100% | |
SeraSeq FFPE Tumor Fusion RNA Reference Material | 10–258 copies | FUSION | 13 | 32 | 98.6% | 99.3% |
SeraSeq FFPE NTRK Fusion RNA Reference Material | 94–377 copies | FUSION | 15 | 32 | 99.2% | 99.2% |
SeraSeq® Lung & Brain CNV Mix | + 3 copies (5 copies) | CNV | 2 | 32 | 100% | 100% |
SeraSeq® Breast CNV Mix | + 3 copies (5 copies) | CNV | 2 | 32 | 100% | 100% |
Note: Testing was performed at multiple internal R&D laboratories as part of product verification testing. Samples were run at different plexy levels. Additional verification and validation testing will be performed using the Oncomine Precision Assay and FFPE controls; therefore final performance values can change.
* Indicates observed allele frequency using Oncomine Precision Assay on Genexus System.
Range | Variant type | # of variants per sample | # of sample replicates | Sensitivity | PPV |
0.33% + 0.17% SD AF* | SNV | 67 | 32 | 89.2% | 100% |
INDEL | 4 | 32 | 100% | 100% | |
1.16X fold change | CNV | 1 | 32 | 100% | 100% |
1% Tri-Fusion and MET Exon 14 Skip in Total RNA | FUSION | 1 | 32 | 97.7% | 96.4% |
NOTE: Testing was performed at multiple internal R&D laboratories as part of product verification testing. Samples were run at different plexy levels. Additional verification andvalidation testing will be performed using the Oncomine Precision Assay and FFPE controls; therefore final performance values can change.
* Indicates observed allele frequency using Oncomine Precision Assay on Genexus System.
Learn more about Oncomine solutions for precision oncology at oncomine.com.
For Research Use Only. Not for use in diagnostic procedures.