Sage™ QS 32plex is ideal for clinical laboratories running high throughput NIPT
Providing laboratories with enhanced flexibility, scalability and sequencing efficiencies, while retaining all the high qualities of the existing Sage™ test
Sage™ QS 32plex offers a flexible, personalised, cost-effective workflow
Key Features
Innovative technology for fetal fraction enrichment
The Yourgene QS250 allows high-throughput target enrichment of cfDNA NGS library constructs prior to sequencing, enabling great improvements in fetal fraction enrichment. In addition to gel size selection, it also allows fragment analysis and solution-based fluorescence quantification assays with a single piece of equipment
NGS workflow
Sage™ 32plex runs on the Thermo Fisher Ion Torrent sequencing technology. Sage™ QS32 plex solution significantly improves efficiency, enabling up to 32 samples to be processed in one sequencing chip. However, the workflow is scalable and flexible with automated or manual options, robust prenatal screening software
Clinical coverage
The Sage™ prenatal screen offers screening on a wider range of clinical conditions, including trisomy 21, trisomy 18 and trisomy 13, sex chromosome aneuploidies
Rapid, automated prenatal screening software
Sage™ Link, a custom built cloud-based bioinformatics portal, recently enhanced with additional features and an improved user-friendly interface. The resulting data is processed so a small data file can be easily, quickly and safely uploaded to Sage™ Link. No bioinformatician is required to analyse the data, a simple to interpret screening test report is generated for each patient sample
World class technical support
Our international technical support team is well regarded by our laboratory customers. Feedback is exemplary that they provide excellent and detailed training programmes, pre and post installation support, hand-holding and ongoing support once up and running