Transform your services
Deliver richer multiomic insights via scalable innovation
Attracting service projects in a competitive environment means navigating technology evolution alongside technical and operational risk to deliver differentiated, high-quality data. Service Providers tell us that strong technology partnerships are essential to becoming trusted experts for their users.
Our Service Provider Programme supports labs like yours delivering technology innovation, scalable usability, and partnership to attract projects and deliver richer, multiomic insights to your users.
Show your scientific community what they've been missing
Empower your users to ask bolder questions and enhance their decision-making. Unlock multi-layered insights using a single multiomic platform that directly sequences native DNA and RNA — with simultaneous methylation detection. Detect more variation with high accuracy in complete genomes, transcriptomes, epigenomes, targeted regions, plasmids, and amplicons.
Don't let technology limit discovery and decision-making
19% of the human genome is inaccessible to legacy short-read sequencing technology¹
<3% of all CpG sites are covered by standard genotyping approaches²
40% of all structural variants are missed by legacy short-read sequencing technology³
Deliver greater insights on a single, streamlined platform
Richer insights
Highly accurate genomic data that captures more types of genetic variation
- ✔️ Any read length — short to ultra long
- ✔️ Phasing and structural variants inaccessible to legacy technologies
- ✔️ Full-length transcript isoforms at single-cell resolution
Faster results
Near-sample, real-time workflows that don't require batching
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Accessible and affordable
Scalability that enables every application
➡️
- ✔️ Built-in, best-in-class methylation detection
- ✔️ SNV accuracy comparable to short-read sequencing
- ✔️ Complete genome assemblies, including dark regions
Explore platform performance at: nanoporetech.com/accuracy.
Our Service Provider Programme supports the growth of your service
Connect
Promote your Oxford Nanopore service and build your project pipeline.
- Supercharge your online presence with our marketing resources, and advertise on nanoporetech.com
- Deliver engaging user events with your Oxford Nanopore team and our seminar toolkits
- Receive direct project referrals from our website, events, and sales teams
Accelerate
Speed up your project workflow with specialised tools and support.
- Quickly estimate project costs using our online calculator
- Streamline your lab work with sample-to-answer protocols and simple EPI2METM data analysis
- Access expert support when you need it, for ordering, application setup, and complex projects
Expand
Enrich the value of your service menu for your user community.
- Stay at the cutting edge of application and platform developments via newsletters and events
- Explore new applications, user benefits, and lab requirements on our online Service Provider hub
- Develop your differentiated service portfolio with expert support and investment in optional Workflow-Trained application trainings
Expand your service portfolio with complete sample-to-answer workflows and training
Expand your service offering by selecting from applications with optimised workflows that are recommended for service providers to simplify implementation.
Invest in optional Workflow-Trained training to streamline application integration and create marketable differentiation for your service. Sequencing workflow applications include:
[human-dna-icon]
Human whole genome
Simultaneous variant and methylation detection
[cell-icon]
Single cell
Comprehensive isoform-level analysis
[target-icon]
Amplicons
Targeted sequence and variant detection
[plasmid-icon]
Whole plasmid
Fast, full-length characterisation
[bacteria-icon]
Bacterial isolates
Assembly and identification
[rna-icon]
Direct RNA
Simultaneous sequence and methylation detection
Data analysis for all levels of expertise
Enjoy free access to our powerful EPI2ME platform. Available through an intuitive interface or the command line, the pre-packaged, open-source EPI2ME workflows offer streamlined analysis of Oxford Nanopore sequencing data for you and your service users.
For data scientists comfortable with command-line interfaces, the latest basecallers, EPI2ME workflows, and cutting-edge tools can be found in the Oxford Nanopore GitHub repositories. You can also integrate your own code into our workflows. Full technical support ensures rapid, efficient delivery of maximum data insights.
Find out more at: nanoporetech.com/analyse.
Get started whatever your budget, and scale up easily
Choose from project-scale and production-scale GridION™™ and PromethION™™ sequencers with integrated compute, designed for plug-and-play installation without additional calibration. Independently controlled flow cell positions support flexible, on-demand sequencing run multiple samples and multiple applications simultaneously on a single device. Maximise your device capacity and never waste time waiting for sample batching.
Explore our devices at: nanoporetech.com/sequence.
The document displays images of Oxford Nanopore sequencing devices: GridION (a compact unit with multiple ports) and PromethION (a larger, more complex system). These are described as project-scale and production-scale sequencers.
"... with few exceptions, there's only one real choice, and that's Oxford Nanopore"
— Prof. Steven Salzberg, Johns Hopkins University, USA⁴
Want to learn more?
For more information on how our Service Provider Programme can help your team and scientific community unlock richer genomic insights, visit: nanoporetech.com/service-provider-programme.
For any questions or to arrange a meeting with one of our sequencing experts, email: support@nanoporetech.com.
References
- Ahsan, M.U., Liu, Q., Fang, L., and Wang, K. NanoCaller for accurate detection of SNPs and indels in difficult-to-map regions from long-read sequencing by haplotype-aware deep neural networks. Genome Biol. 22, 261 (2021). DOI: https://doi.org/10.1186/s13059-021-02472-2
- Flynn, R. et al. Evaluation of nanopore sequencing for epigenetic epidemiology: a comparison with DNA methylation microarrays. Hum. Mol. Genet. 31(18), 3181–3190 (2022). DOI: https://doi.org/10.1093/hmg/ddac112
- Beyter, D. et al. Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits. Nat. Genet. 53, 779–786 (2021). DOI: https://doi.org/10.1038/s41588-021-00865-4
- Marx, V. Method of the year: long-read sequencing. Nat. Methods 20, 6–11 (2023). DOI: https://doi.org/10.1038/s41592-022-01730-w
