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Speak to our expertsWe 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
Inherited genetic variants play a critical role in a wide range of diseases, enabling earlier diagnosis, informed clinical management, family screening, and personalised patient care. The YouSeq Inherited Disease Panel provides researchers and clinical laboratories with a comprehensive targeted NGS solution for the confident analysis of hereditary disease risk across multiple clinical specialties. Our comprehensive 333-gene panel covers clinically relevant genes associated with cancer predisposition, endocrine disorders, immunodeficiency, ophthalmology, neurogenetics, neurodegeneration, and monogenic diabetes. Designed for clinical research applications, the panel is available as predefined subpanels for specific disease areas or as a fully customisable product, allowing genes to be added or removed to meet your exact research requirements. Ideal for high-throughput laboratories, the panel delivers robust variant detection with focused genomic coverage, providing the sensitivity, efficiency, and scalability needed to support a broad range of inherited disease research workflows.
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.
13 NGS products
Frequently asked questions
What is PhiX?
What does Read Length mean?
What does a 'library' mean?
What are the three types of Reads that can be performed with Illumina based sequencing?
What is read depth?
Can I use your custom panel on an iSeq/MiSeq/HiSeq/NovaSeq?
What causes variability in qPCR Library quantitation data?
What is included in the One 16S kit?
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