Download our new Application Note about the Hereditary Cancer Solution (HCS) by SOPHiA GENETICS, which represents a comprehensive NGS application for the detection of genomic variants in 26 genes associated with breast and ovarian, as well as digestive cancers. In addition, the HCS is the first CE-IVD capture-based application.
In this Application Note, is described the automation of the solution on a Hamilton Microlab STARlet. The automation permits the standardization of the genomic analysis in clinical setting, reduce the bias due to manual sample preparation and facilitate the sample and reagents traceability.
- Standardization of genomic testing in clinical settings
- Reduction of bias due to manual sample preparation
- A comprehensive NGS application for the detection of genomic variants
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