Cell3™ Target: Tumor Exome
Tumor exome sequencing
Whole exome capture with extensive clinically relevant content for comprehensive primary tumor sequencing.
Tumor relevant content
Whole exome capture designed specifically for cancer research covering key intronic regions like promoters, translocations and fusions and CNVs.
Range of sample types
Our tumor exome supports a broad range of sample types, including formalin-fixed, paraffin-embedded (FFPE) DNA, FF, gDNA and cell-free DNA (cfDNA).
Optimised performance
Delivering excellent uniformity of coverage, Cell3™ Target Tumor Exome reduces sequencing costs and improves sample throughput.
Customisable
Designed to be flexible, Cell3™ Target Tumor Exome allows you to add extra content to cover targets specific to your project.
Primary tumor sequencing
By focusing on the coding regions of the genome, whole exome sequencing offers a cost-effective solution for primary tumour profiling when compared to whole genome sequencing. It allows for deeper sequencing enabling more sensitive mutation detection and improved tumor mutation burden (TMB) calling versus smaller panels.
However, many mutation types that are known to be important in cancer, for example tumor promoters like TERT, translocations and fusions or CNVs, are not covered by standard exome enrichments. At Nonacus, we believe a different type of exome is required for cancer research.
Tumor relevant content for cancer research
The Nonacus Cell3™ Target Tumor Exome is based on our standard Whole Exome product enhanced with baits from our Pan-Cancer panel. It includes enhanced coverage of the most clinically relevant genes from NCCN/FDA cancer treatment guidelines, 116 cancer driver genes and 345 genes in vital cancer signalling pathways. The design, whilst exon focused, covers key intronic and promoter regions like the TERT promoter and translocations and fusions. It also contains genome-wide CNV probes to support robust copy number calling. At 37.3Mb, it is a comprehensive panel that allows you to accurately identify and profile novel and known variants associated with cancer.
Reliable sequencing for primary, metastatic or liquid biopsies
We know that you may want to use the same exome product on multiple sample types – especially when, for example, carrying out tumour/normal comparisons. The Cell3™ Target Tumor Exome kit has been developed for and validated on broad range of sample types, including formalin-fixed, paraffin-embedded (FFPE), fresh frozen, genomic and cell free DNA.
Low input FFPE and cfDNA sequencing.
Using from as little as 1 ng of genomic or cfDNA, with optimised protocols for FFPE our tumor exome unlocks the door for many oncology applications
Detect low frequency variants in primary tumors
The Cell3™ Target library preparation behind our tumor exome enrichment incorporates error suppression technology. This includes unique molecular indexes (UMIs) and unique dual indexes (UDIs), to remove both PCR and sequencing errors and index hopping events.
Figure 1. Using UMI’s to identify and quantify individual DNA molecules during library preparation increases sensitivity
Optimised sequencing performance
The baits used in Cell3™ Target Tumor Exome are designed to deliver excellent uniformity of coverage. By improving uniformity of coverage and reducing the number of low coverage exons, our tumor exome enrichment optimises sequencing efficiency and sample capacity per sequencing run.
Customise content for cancer profiling
Designed to be flexible, Cell3™ Target Tumor Exome allows you to add extra content specific to your project. Whether this is additional content or increased coverage of existing content, our Panel Design Tool makes this a simple and easy process to implement. And our rapid production turnaround means you will receive a fully NGS-validated custom exome within weeks.
- Additional content with high enrichment uniformity
- Increased coverage of specific genes covered by Cell3™ Target Tumor Exome
- Optimization of spike-in ratio
Log into the Probe Design Tool at MyNonacus to start the design process and get a quote or drop us an email at info@nonacus.com
Ordering Information
Cell3 Target panels are available with one of two versions of our library preparation kits:
-Fragmentation: for use with gDNA (FF or FFPE)
-Non-Fragmentation: for use with cell free DNA
| Cell3™ Target: Tumor Exome, Frag 16 samples | NGS_C3T_TEX_FR_16 |
| Cell3™ Target Tumor Exome Frag 96 Samples | NGS_C3T_TEX_FR_96_A/B/C/D* |
| Cell3™ Target: Tumor Exome, Non Frag 16 samples | NGS_C3T_TEX_NF_16 |
| Cell3™ Target: Tumor Exome, Non Frag 96 samples | NGS_C3T_TEX_NF_96_A/B/C/D* |
* To provide flexibility in multiplexing samples, our 96-sample kits offer a choice in adapter plate:
A = Adapter plate with indexes 1-96
B = Adapter plate with indexes 97-192
C = Adapter plate with indexes 193-288
D = Adapter plate with indexes 289-384
Product Resources
Detailed product information available to download.
For Research Use Only. Not for use in diagnostic procedures.
Product Support
If you have a query relating to any of our products, please take a look at our FAQs or complete our Contact me form and one of our team will get back to you as soon as possible.
We offer several NGS cancer panels including the Hereditary Cancer Panel, Bladder Cancer Panel, Pan-Cancer TMB/MSI (524) Panel, Actionable Mutation Panel (EGFR), Whole Exome, and Custom NGS panels.
Learn more about our products for oncology
Pan-Cancer TMB/MSI (524) Panel
A comprehensive panel of 524 oncogenes that allows you to accurately profile and stratify all common cancers and predict response to immunotherapy.
Actionable Mutation Panel (EGFR)
A highly focused panel covering actionable mutations in the EGFR pathway.
Custom NGS panels
Target the genes and variants important to you by creating your own NGS panel using our ultra-sensitive Cell3™ Target technology
Pre-Analytical Products
Products for the collection, stabilisation and extraction of cell-free DNA