Sold by: InocrasÂ
CancerVision is a cutting-edge 2-in-1 whole-genome cancer assay offering both somatic (40x) and paired germline (20x) coverage, with ultra-deep targeting (500x) of 600+ clinically relevant cancer genes. It delivers >99% sensitivity and PPV, with robust detection of complex variants including SVs, CNVs, and mutations in non-coding regions. CancerVision also provides key biomarker insights such as TMB, MSI, HRD, mutational signatures, and germline variants. This CAP/CLIA-validated assay offers a fast 2-week turnaround and supports advanced custom analyses, including ecDNA, tumor ploidy, and transposable element detection, at whole-genome resolution. Designed for precision oncology, CancerVision is your comprehensive genomic solution for cancer diagnostics and research.
Overview
The CancerVision assay is a comprehensive whole-genome sequencing (WGS) tumor profiling test specifically designed for patients with solid tumors. A key feature of this assay is its ability to detect a broad spectrum of genomic alterations, including single nucleotide variants (SNVs), small indels, structural variants (SVs), and copy number variants (CNVs), providing a detailed and complete picture of the cancer's genetic makeup. The test also incorporates paired somatic-germline testing, which is crucial for a thorough analysis. For cases where tissue samples are not viable, CancerVision offers a liquid biopsy option, ensuring flexibility and accessibility. The assay is also designed to provide valuable genome-wide signatures, such as Tumor Mutational Burden (TMB) and Microsatellite Instability (MSI).
The benefits of the CancerVision assay are significant, especially for providers seeking to make informed treatment decisions. It has been clinically validated and proven to detect 100% of variants identified by conventional NGS panel tests, demonstrating its high sensitivity and reliability. The comprehensive nature of the report helps to alleviate the diagnostic burden on providers by translating complex genetic data into clear, actionable insights, with over 70% of reports yielding clinically relevant information. This is made possible by an AI-powered bioinformatics pipeline built on the secure and scalable AWS infrastructure. Inocras also ensures a streamlined process for results with an efficient two-week turnaround time and access to expert medical consultations, making the integration of this advanced technology into clinical practice both simple and effective.
Highlights
- Get a complete view of solid tumors with our paired somatic (40x)-germline (20x) whole genome profile. We also include a high-depth 600-gene target panel (500x) for a robust and in-depth analysis.
- Clinically validated with >99% sensitivity and positive predictive value. Our platform ensures highly accurate detection of complex variants (SV, CNV) and analyzes non-coding regions for a complete genomic profile.
- Our proprietary algorithms provide essential genome-wide signatures (TMB, MSI, HRD) with every report. For advanced research, custom whole-genome level data and analysis (e.g., ceDNA, tumor ploidy, transposable elements) are available upon request.
Details
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Delivery method
Deployed on AWS
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Pricing
Pricing is based on actual usage, with charges varying according to how much you consume. Subscriptions have no end date and may be canceled any time.
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Dimension | Description | Cost/unit |
|---|---|---|
CancerVision | Payment per unit of analyzed and interpreted report | $4,000.00 |
Vendor refund policy
Refunds are available if: (1) you cancel before your sample is received, (2) your sample cannot be processed due to lab error (free re-test or full refund offered), or (3) Inocras cannot perform the CancerVision test due to unforeseen circumstances.
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Delivery details
Software as a Service (SaaS)
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Support
Vendor support
Inocras provides a comprehensive support program designed to ensure a seamless experience for every user, from initial sample submission to final data delivery. We offer full program management services, giving you real-time updates on your samples and project progression. Our dedicated team tracks each stage of the process, from sample receipt and quality control to sequencing and bioinformatics analysis, providing you with transparency and peace of mind.
A cornerstone of our support is the 24/7 access to our expert Lab Support Team. We understand that questions can arise at any time, and our team is always on standby to provide assistance. Whether you need clarification on sample requirements, have questions about your report, or require guidance on data interpretation, our specialists are ready to help. This direct line of communication ensures that you receive timely and accurate answers, empowering you to make the most of our genomic insights. For any inquiries, our support team can be reached directly at lab@inocras.com . We are committed to being a trusted partner in your work, providing not just cutting-edge genomic data, but also the continuous, high-quality support you need to succeed.
AWS infrastructure support
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