Curated Pan-Cancer Content
- Mutation, CNV and fusion variant types across 50 key genes
- Driver and resistance variants
Introducing the first turnkey NGS system that automates the specimen-to-report workflow and delivers results in a single day. With just 10 minutes of hands-on time and two touch points, users can get up and running quickly with significantly less training. This highly flexible system lets you cost-effectively process samples as they come in - even just one.
Learn the benefits of the Genexus System.
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Now you don’t have to wait to access the Genexus System. We are committed to supporting your
research by offering a wide range of financial and leasing programs for even easier adoption of NGS.
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The Oncomine Precision Assay features carefully curated biomarker content spanning 50 genes based on the latest therapy developments, medical guidelines, and clinical trials. Enhanced fusion detection provides broad coverage for the most prevalent isoforms, along with novel fusions. You have the option to profile DNA or RNA from plasma or lysate derived from FFPE samples, giving you a wide range of utility. All of this is provided with a one-day turnaround time and a highly automated workflow on the Genexus System.
Did you know that high sample input requirements significantly limit the usability of hybrid capture-based NGS tests? You might assume that all NGS tests are created equal. However, recent data from more than 20 US laboratories has shown that small biopsies and low-tumor content samples can pose significant challenges for some tests - some labs have test failure rates of 58%.
This means that less than half of all samples will be successfully sequenced. Not with Oncomine Solutions. You can experience a sequencing success rate of over 95% with only 10ng of nucleic acid input. Get NGS results for most of the precious samples you have.
Gene fusions are an increasingly important target in precision oncology. Oncomine assays are superior for both sequencing success rate and sensitivity, two critical factors for fusion detection. Even when the tissue is very limited or the variants exist at low levels in the sample, you can detect key fusions by combining:
Are you worried about NGS bioinformatics? Using different software and requiring an expert to stich it all together? No need anymore! The Genexus Software, one secure, streamlined and easy-to-use NGS analysis software, provides a seamless experience from end to end, starting with entering sample data and finishing with report.
The Oncomine Reporter delivers clear and concise reports that present all relevant variants with annotated information about targeted therapies, guidelines, and enrollment of ongoing clinical trials.
The report is customizable so that you can tailor it to fit your team's needs.
Learn More About Oncomine Informatics
A molecular biology laboratory at the Hospital Universitari Vall d'Hebron performs NGS analysis with the Genexus System.
The Oncomine Precision Assay on the Ion Torrent Genexus System detects low-level variants that are particularly important for liquid biopsy testing. It provides:
Although tissue samples are still the gold standard for molecular profiling, there exist many limitations.
Tissue can be inaccessible or there may not be enough material to sequence. Further, obtaining a tissue sample is difficult to repeat and not useful for monitoring and the sample may not reflect tumor heterogeneity. Liquid biopsy may be a viable alternative to tissue sequencing, as it is minimally invasive, provides a comprehensive tumor profile, and allows for repeat sampling.
With the Oncomine Precision Assay, you have the flexibility to sequence standard tissue or minimally invasive plasma samples, from one test on a single workflow.
