The ultimate multiplexing technology
We believe NGS is the ultimate tool for molecular multiplex target detection. The ability to detect thousands of targets at once fits beautifully with our vision to build the ultimate multiplexed diagnostic test.
YouSeq’s next generation sequencing products are engineered to make NGS library preparation fast, reliable and extraordinarily scalable for research and diagnostic laboratories. Our ever-growing NGS product menu spans inherited risk factors, microbiome panels, and more — giving customers the power to rapidly sequence entire target sets with high uniformity and consistent performance. All kits are supplied with optimised library prep chemistry, streamlined sample-to-sequence workflows and bioinformatic pipelines that make interpretation faster and easier.
NGS Panels
Our new Inherited Cancer Panel — launching now — extends this same philosophy into human predisposition testing. It covers a comprehensive set of high-value cancer predisposition genes across pathways including breast/ovarian cancer, Lynch syndrome / MMR genes, and other hereditary cancer risks — all packaged in a single streamlined assay with simple NGS library preparation.
Unlike other Inherited/Germline Cancer NGS solutions, YouSeq provides an all inclusive sample-to-report workflow containing all the reagents you need from library preparation to clinical grade reports.
Crucially, YouSeq also offers fully custom NGS panel development. If a lab or research group needs a bespoke gene set, we can design and manufacture custom NGS kits covering ANY chosen collection of genes, deletions, SNPs or other targets for research and clinical-research applications. This lets high-throughput labs build their exact vision of a hyper-multiplexed NGS panel, rather than being restricted to one fixed predefined product.
