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

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

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Frequently asked questions

PhiX is a ready-made DNA library. It’s useful as a positive control to check all is working well with your sequencing run. It also adds “complexity” which is useful. DNA sequencers don’t like to sequence multiple identical libraries at the same time so adding PhiX mixes things up a bit and helps your sequencer perform better.
The number of bases sequenced by your sequencer as a continuous length.
A collection of DNA or cDNA fragments prepared for sequencing by a performing a series of enzymatic steps. These steps are commonly referred to as the Library Preparation.
- Single-End Read (SE), which provides sequence from only one end of the DNA insert - Paired-End Read (PE), which provides sequence from both ends of a DNA insert - Mate Pair Read (ME), Similar to paired-end but both reads come from a single strand of DNA
The number of times a nucleotide is sequenced. The deeper the read depth, the higher degrees of confidence in the base calls.
Yes, YouSeq custom panels can be used on all illumina platforms.
Inaccurate liquid handling is the most common reason for variability. We are happy to give guidance on good pipetting technique and good laboratory practice. Even simple things like ensuring that all standards are thoroughly vortexed to ensure they are correctly resuspended will help to ensure good data quality.
We supply everything that is required for the library preparation side of the workflow. We would expect the customer to have the usual molecular laboratory tools available to them.

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