Cancer All-In-One Custom NGS Assays
Custom hybrid capture NGS assays detecting all somatic cancer variants in a single DNA workflow.
- Streamlined profiling of SNV, indel, CNV, and translocation from a single DNA sample of 50 ng or less
- Support for FFPE samples and low-quality DNA samples
- From DNA to target-enriched NGS libraries in less than a day
- Robust detection of somatic CNV, including gene amplification and deletion, in 15% or lower clone fraction
- High sensitivity genomic translocation detection by fusion-driver gene finds breakpoint and identifies fusion partner
- Custom panels targeting all 4 types of variants easily created using SureDesign in under an hour
- Create custom panels by selecting genes from the Agilent predefined cancer gene set or any genes in the Refseq database