Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world

Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world

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Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started.

Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started.

Our next-generation sequencing and greater fidelity chemistry is not only transforming research. It’s enabling life-changing precision health at scale.

We’re the same great team with the same commitment to quality, but now you can browse a larger range with much greater ease and selling points to say why this is a benefit to you.

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Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world

Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started.

In other words, we feel the track record of the people and the products at Thistle will stand up to the challenges that lie ahead. We invite you to test our commitment at all times.

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Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started.

Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world

Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started.

Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started.

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Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world

No matter your area of expertise, we’ve got you covered. Our full genomic solutions are designed to drive your research or clinical application to the next level.

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At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. As a global company that places high value on collaborative interactions, rapid delivery of solutions, and providing the highest level of quality, we strive to meet this challenge. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics.

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Deeper studies, more samples, more modalities. The NovaSeq X and 25B flow cell make ultra-high depth multiomics more accessible.

We would like to thank you for taking time to consider us for your valued business. Please don’t hesitate to call us if we can be of assistance.We now have a network of seven sales representatives throughout the UK who are capable of providing full technical support on all the products listed. Call 01698 338844 should you require a visit from one of our team.

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Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world

Explore the research, applications, and changemakers catalyzing genomics. Featured news and analysis to unite, inspire, and feed our collective curiosity.

Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world

The mission has always been clear: to improve human health by unlocking the power of the genome. That’s why we push the boundaries of genomic possibility so that researchers and clinicians can further accelerate their discoveries and applications to heal people and the planet.

The staff at Thistle Scientific Ltd., are determined to offer and maintain the highest of standards in terms of customer care. Our philosophy is therefore straightforward:

Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started.