Empowering through State-of-the-Art Sequencing Services Across Norway

NorSeq is supported by a generous grant from The Research Council of Norway (RCN), enabling continuous investment in cutting-edge sequencing technologies. Our facilities provide access to a wide range of high-throughput sequencing platforms, ensuring cost-efficient and high-quality data generation for research and clinical projects.
Available sequencing platforms:
• Illumina: NovaSeq 6000, HiSeq 4000, NextSeq 500/550, and MiSeq
• Oxford Nanopore Technologies: GridION
• Pacific Biosciences: Sequel II
All NorSeq sites are equipped to support researchers through every step of the sequencing workflow — from project design and sample preparation to data generation and bioinformatics analysis. Our expert teams provide tailored advice on choosing the most appropriate technology, library preparation, and sequencing strategy for each project.
NorSeq operates as a nationally coordinated network connecting the leading sequencing facilities in Oslo, Bergen, Trondheim, and Tromsø, ensuring efficient collaboration, shared expertise, and the most cost- and time-effective solutions for users across Norway.
With a commitment to data security, transparency, and scientific excellence, NorSeq continues to advance national capacity in genomics and personalized medicine.
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01

High-Throughput Sequencing

Our high-throughput sequencing services offer researchers and institutions cutting-edge technology to efficiently process a vast amount of genomic data. With our state-of-the-art sequencing platforms, we facilitate comprehensive studies that enhance understanding of genetic variations and their implications in health and disease. Clients benefit from our expertise in optimizing protocols and analyzing results, ensuring high-quality data that drives scientific discovery and innovation in personalized medicine.

02

Bioinformatics Services

NorSeq provides expert bioinformatics services that empower researchers to interpret complex genomic data effectively. Our team utilizes advanced algorithms and software tools to analyze and visualize sequencing results, ensuring meaningful insights into genetic information. We collaborate closely with researchers to customize analyses to their specific needs, supporting them in their pursuit of groundbreaking scientific inquiries and enhancing the efficiency of their research projects. This service serves as an integral component of our mission to advance genomics in Norway.

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Close-up of a colorful abstract representation of DNA strands, illustrating science and genetics.
03

Sample Preparation

Our sample preparation services guarantee high-quality DNA and RNA isolation, enabling accurate and reproducible genomic analysis. We follow rigorous protocols and quality control measures to handle samples, ensuring integrity from collection to processing. Our expert team supports researchers in selecting the most appropriate methods based on the type of samples and intended applications. This essential service lays the foundation for reliable sequencing results and comprehensive downstream bioinformatics analysis, thus facilitating groundbreaking genomic research.

04

Collaborative Research Support

NorSeq is dedicated to fostering collaborative research partnerships across Norway. We work closely with academic institutions, healthcare providers, and industry stakeholders to create synergies that advance genomic research and personalized medicine. By providing access to our state-of-the-art facilities, expertise, and resources, we encourage innovation and knowledge sharing. Our goal is to build a responsive network that facilitates groundbreaking studies, ensuring that the latest advancements in genomics are effectively translated into clinical practice and improved healthcare outcomes.

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