Automated nanopore sequencing library prep for native DNA/RNA fragments

Automate high-throughput nanopore library prep with DreamPrep NGS solutions

5 Apr 2023
James Li
Blood Banking Scientist

Product news

The Tecan Group and Oxford Nanopore Technologies plc announced their collaboration to drive easier high-throughput nanopore library preparation in an automated way. The result is a fully walkaway automated workflow for the Oxford Nanopore Ligation Sequencing Kit XL V14 protocol (LSK114) with Tecan DreamPrep NGS solutions. The LSK114 protocol allows for any fragment length of DNA to be sequenced, which can range from cell-free DNA to amplicons to any length DNA fragments, from 200 base pairs to more than 100kb or even Mb. This is a major advance over traditional sequencing platforms and protocols that can only sequence short fragments typically in the range of 300 to 600 base pairs.

Sequencing native, long fragments of DNA is beneficial to generate more comprehensive insights into the genome – which often contain methylation, repetitive patterns of sequences or larger-scale genetic variants – as well as reaching parts of the genome that cannot be resolved by using traditional short read technologies in the same single sequencing run. Having complete genome assemblies is necessary to ensure better understanding of chromosome function, human disease, and genomic variation, which will translate in future to better prediction and management of diseases. Therefore, by combining highly reproducible automated library preparation of short and/or long fragments and high yields of genomic data, it becomes feasible to reliably identify a comprehensive map of genetic alterations, conduct accurate phasing, resolve repeated sequences, and measure DNA methylation, all in a single sequencing run. Being able to deploy the same workflow on shorter, native fragments, such as cell-free DNA, opens opportunities in methylation analysis and exploration of the complete cell-free DNA fragments in a sample, the ‘fragmentome’.

“At Tecan we scale healthcare innovation, from life science to the clinic, and our partnership with Oxford Nanopore enables us to do just that,” said Dr. Klaus Lun, Tecan Executive Vice President and Head of the Life Sciences Business Division. “We bring push-button, walk-away convenience to high-throughput library preparation workflows, enabling scientists to focus on new discoveries instead of tedious manual work. Combining our expertise in automation and high-quality library preparation with Oxford Nanopore sequencing and its capabilities around any-length reads, native DNA/RNA and real time sequencing, has implications in multiple fields, from population genetics to cancer research and personalized medicine.”

Oxford Nanopore CEO Gordon Sanghera added, “Our goal at Oxford Nanopore is to deliver affordable and accessible plug-and-play platforms for biological analyses that are currently performed, and open new applications that have a profound, positive impact on improving our understanding of genetic alterations linked to disease. Our technology now provides an automated solution in one platform, providing a comprehensive genomic data that includes methylation, structural variation and copy number variation, as well as standard snp and snv, calling for all biological questions including methylation in the same sequencing run. Our collaboration with Tecan is scaling accessible life sciences innovation with a global partner, providing automated seamless plug-and-play solutions to our customers in quicker, higher quality results that save time, cost and effort.”

Oxford Nanopore technology enables base-modification analysis to be performed alongside nucleotide sequencing on the same single read without the need to run multiple sequencing experiments. Therefore, unlike traditional technologies, no additional complex library preparation with (for example bisulfite sequencing for methylation) is required, and epigenetic modification analysis can be performed across the whole genome during the experiment. Tecan's automated library preparation systems aim to simplify and improve the reliability of laboratory workflows by reducing the time and potential for errors in manual processes. The integrated combination of Oxford Nanopore and Tecan technologies is intended to enhance true load-and-go DNA and RNA sequencing library preparation with proven liquid handling technology, reagent kits that are compatible with automation, and intuitive user interfaces that will allow set-up for walkaway library prep runs in the DreamPrep NGS.

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DNA SequencingDNA sequencing, such as sanger sequencing, is a biological technique that determines the precise order of nucleotide bases in a fragment or template of DNA. DNA sequencers and genetic analyzers are based on capillary electrophoresis, where labeled DNA fragments are electrophoretically separated by size as they migrate through a polymer. Find the best DNA sequencing products, including DNA sequencing kits, genomic libraries and genetic identity kits in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.DNA / RNA QuantificationDetection and quantification of nucleic acids is important in molecular biology, cloning, expression, forensics and clinical diagnostics. Nucleic acids can be detected by labeling with colorimetric, fluorescent or radio labels and using in situ hybridization kits to identify specific sequences. Multiple nucleic acids can be detected and quantified at once using RNA / DNA detection beads or RNA / DNA microarrays. Find the best DNA / RNA Quantification products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.Next Generation SequencingNext-generation sequencing (NGS), also known as whole-genome sequencing, high-throughput sequencing and massive parallel sequencing, produces and analyses thousands to millions of nucleotide sequences at once. Sequencing systems operate via varying technologies depending on the manufacturer, including sequencing by synthesis, ligation, pyrosequencing, ion semiconductor and single-molecule real-time sequencing. For NGS, library preparation is paramount to successful sequencing. In this section, explore a range of library preparation kits, from targeted, amplicon-based or hybridization-based kits including epigenomic, transcriptomic and genomic workflows to fragmentation kits. Find the best next-generation sequencing products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.AutomationAutomation in laboratories and manufacturing processes enhances efficiency, precision, and scalability by reducing the need for manual intervention. It plays a critical role in improving productivity, minimizing human error, and accelerating workflows in fields like diagnostics, drug development, and industrial testing. Automation technologies include robotic systems, automated liquid handlers, and process control systems that streamline complex tasks and ensure consistent, reproducible results. Explore our peer-reviewed product directory to discover the best automation solutions, compare options, read user reviews, and get prices directly from manufacturers.DNA QuantificationDNA quantification is the process of measuring the amount of DNA in a sample. It is vital in genomics, molecular biology, and biotechnology, helping to ensure accurate experiments and data analysis. Explore DNA quantification tools in our peer-reviewed product directory; compare products, check reviews, and get pricing directly from manufacturers.