Swift Colorectal (CRC) Cancer Panel
Interrogate clinically-relevant colorectal cancer genes
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The Accel-Amplicon Plus Colorectal Cancer Panel is an NGS multigene panel for variant discovery and screening. It combines content from peer reviewed publications and other sources to offer comprehensive and exon-level hotspot coverage of 16 clinically-relevant colorectal genes.
The panel is modular, allowing you to add focused content to achieve your most optimal design. Either combine pre-validated content such as our Lynch Syndrome content or add your own targets. We’ll work alongside you to design your assay and then Swift will optimize and wet-bench validate its performance before shipping it to you.
Key features include:
- Robust performance on cell-free DNA and FFPE samples starting with as little as 10 ng input
- Sensitive detection of rare variants down to 1% allele frequency
- Easy, single-tube assay with sequence ready libraries in under 2 hours
- Streamlined analysis with new bioinformatics tools including Primerclip or Genialis
- Compatible with all Illumina sequencers
