![Cancer All-In-One Custom NGS Assays Cancer All-In-One Custom NGS Assays](/cs/publishingimages/Genomics-images_AIO(320x320)_1.0.jpg)
Cancer All-In-One Custom NGS Assays
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.