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Science for Life Laboratory, SciLifeLab, is a national center for molecular biosciences with focus on health and environmental research. SciLifeLab is a national resource and a collaboration between four universities: Karolinska Institutet, KTH Royal Institute of Technology, Stockholm University and Uppsala University.

The center combines frontline technical expertise with advanced knowledge of translational medicine and molecular bioscience. Researchers from all of Sweden can use both the technology and the know-how that is present at SciLifeLab to subsidized fees. Users from commercial companies pay the full costs of the analyses performed.

 

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AH diagnostics are the Nordic distributor for PacBio and a broad range of others supplier of high-quality equipment.
PacBio Sequel Systems support innovative scientists in a wide variety of life science research fields, including human biomedical, plant and animal sciences, and microbiology and infectious disease. With true long reads, a more comprehensive view of genomes, and the highest consensus accuracy available, scientists can access the full spectrum of genetic variation to discover valuable insights not accessible with other technologies.


 
PacBio combines the Sequel systems with an extensive software portfolio designed to elevate your sequencing efforts by bringing exceptional analytical depth to your genetic data. These advanced tools allow you to analyse, visualize, interact, and manage your data, helping you achieve accurate scientific results.

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10x Genomics meets the critical need for long range, structural and cellular information, with an innovative system that transforms short-read sequencing technologies.

 

Our Chromium™ System supports comprehensive genomics and high-throughput single cell transcriptomics. It enables researchers to discover previously inaccessible genomic information at unprecedented scale, including phased structural variants, phased single nucleotide variants, and dynamic gene expression of individual cells—while leveraging their existing sequencing systems and workflows.

Our proprietary 10x GemCode Technology fuels our Chromium System with an innovative reagent delivery system, set of algorithms and turn-key software analysis tools that enable the discovery of previously inaccessible genetic information at massive rate and scale.

 

Oxford Nanopore Technologies has developed the world's first and only nanopore DNA sequencer, the MinION. The MinION is a portable, real time, long-read, low-cost device that has been designed to bring easy biological analyses to anyone, whether in scientific research, education or a range of real-world applications such as disease/pathogen surveillance, environmental monitoring, food-chain surveillance, self-quantification or even microgravity biology.

The MinION is in use by a thriving community of thousands of users in more than 70 countries, enabling a myriad of applications within the traditional laboratory environment and in the field. The GridION and PromethION devices serve users with larger projects or more samples.

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Nordic BioSite is an established growing company, representing top quality manufacturers of validated products for research and diagnostics. This include high quality sample preparation and purification products for sequencing (e.g. single cell and long-read sequencing).

We want to facilitate your research. From Nordic BioSite you can expect a reliable, knowledgeable and trustworthy supplier who will guide you to the right products for your research needs.

We are by your side.

Follow our blog at  https://www.nordicbiosite-blog.com/.

Bionano Genomics, Inc. offers whole genome analysis tools to better understand the genome and its structure. Its high-throughput system Saphyr builds de novo maps of the genome by massively parallel imaging of the longest single DNA molecules in the industry. Bionano genome mapping provides comprehensive structural variation (SV) calls, identifying all types of SVs with sensitivities that far exceed those based on next-generation sequencing. When combined with orthogonal sequencing data, Bionano maps can provide the correct structure, order, and orientation to assemble reference-quality genomes.
For more information, please visit www.bionanogenomics.com

Silver Sponsor

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Agilent is a leader in life sciences, diagnostics and applied chemical markets. The company provides laboratories worldwide with instruments, services, consumables, applications and expertise, enabling customers to gain the insights they seek. Agilent’s expertise and trusted collaboration give them the highest confidence in our solutions.


Using automated parallel capillary electrophoresis, our Agilent Fragment Analyzer systems offer nucleic acid quality control for a range of applications, including NGS libraries and cfDNA QC.


Our Agilent FEMTO Pulse system is the first ever parallel capillary electrophoresis instrument using a pulsed-field power supply  and able to resolve DNA smears and DNA fragments through 165,000 bp. A meticulously designed optical detection platform enables unprecedented sensitivity, detecting nucleic acids into the lower femtogram range.

RevoluGen is a UK-based, biotech company. The two lead products it has developed are called Fire Monkey and Fire Flower. 

 

Fire Monkey is a High Molecular Weight (HMW) – DNA Nucleic Acid Isolation and Purification (NAIP) kit. It is spin-column based and protocols result in bacterial or mammalian DNA extracts with fragment mass averages of 100kb or above within one hour. In addition, Fire Monkey extracts are of high purity and yield as well as lacking a great amount of smaller DNA fragments that would be extracted with other spin-column kits. This intrinsic size-exclusion aspect of the Fire Monkey extraction process means that Fire Monkey DNA can produce sequencing results with N50s of ~50kb for standard long-read sequencing protocols.


 

Fire Flower is a 10 minutes size selection spin-column based process that greatly reduces the number of DNA fragments shorter than 10kb long, thereby raising the average DNA fragment length in the sample whilst still being compatible with all extraction and sequencing techniques.

 

These, patent protected and externally validated, products are just becoming available commercially directly from RevoluGen and eventually through major distribution channels.

NGI Collaboration Partner

NGI Collaboration Partner

Samplix has developed a novel targeted DNA enrichment technology called PINS suitable for long read as well as short read sequencing.
The PINS enrichment technology is based on physical separation of long DNA fragments into millions of picoliter droplets. The droplets containing the target DNA are identified using ddPCR, physically sorted and the target DNA fragments are then amplified using multiple displacement amplification. Applications include: De-novo sequencing, highly variable and partially unknown sequences, large structural variations, phasing of mutations, repeat regions, GC-rich regions, and samples in limited amount.
 

NGI Sweden / SciLifeLab

@2019 by NGI.

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