SureSelect Cancer All-In-One Custom NGS Assays
The SureSelect Cancer All-In-One Custom solution enables custom NGS assays for streamlined profiling of somatic SNV, indel, CNV and translocation in a single workflow. Custom Cancer All-In-One panels can be created in under an hour using the SureDesign web portal with specialized probes for specific types of variants.
Powered by the SureSelect target enrichment workflows featuring 90-min hybridization, NGS libraries can be generated from low input DNA in less than a day. Robust and confident detection of somatic variants is supported by the SureCall software with our new state-of-the-art CNV and translocation algorithms.
Note: SureCall software currently does not support CNV and translocation detection in the same gene.
For Research Use Only. Not for use in diagnostic procedures.