Nanopore service providers update: three new providers, and more
With the addition of three new service providers, we recap some of the work that is underway around the world by labs offering nanopore sequencing as a service.
KeyGene

KeyGene has always been frontrunner in the application of new sequencing technologies for crop improvement and believes that long reads are crucial to generate high-quality reference genomes. Since its introduction in 2014, KeyGene used ONT’s MinION to sequence plant pathogens, BACs, amplicons and complex crop genomes. Also the ability to directly sequence RNA will disrupt the current short-read oriented field and enable many new applications.
KeyGene is excited about the ability to sequence truly complex plant genomes with Oxford Nanopore’s platforms in just a few days. De novo whole genome sequencing and analysis will be the standard going forward.
Interested to hear more about KeyGene’s achievements on nanopore sequencing? We will present our latest results on sequencing and assembly of lettuce genomes at the London Calling conference in May. Hope to see you in London!
Microbes NG

We are looking forward to advancing our enhanced genome service, if you would like more information please contact us.
Sequencing Platform of I2BC

BaseClear & Future Genomics Technologies

University of Illinois at Urbana-Champaign
The DNA Services unit of the Roy J. Carver Biotechnology Center, University of Illinois at Urbana-Champaign, one of the first Oxford Nanopore Certified Service Providers to offer sequencing with the GridION, has been consistently achieving complete de novo assembly of microbial genomes into one scaffold, as well as the full assembly of all their associated plasmids. The high output and long reads obtained with the 1D libraries enable full assembly of up to 10 microbial genomes per flow cell, bringing the cost of microbial assembly to a few hundreds of dollars. A low coverage of short reads is used to correct indels that remain after polishing of the Oxford Nanopore assembly. The technology has also enabled the facility to fully sequence the genomes of several fungi. It is currently being used to assemble the genomes of several nematodes and also to generate long reads for eukaryotic species with large genomes, to provide more contiguity to existing assemblies.
Additionally, we have been performing full length cDNA sequencing, which has enabled a more thorough characterization of splicing variants in RNA samples than what can be obtained with short reads. An application that is being developed and had produced strong preliminary results in the sequencing of full-length 16S rRNA amplicons constructed with the Fluidigm system. This application yields millions of reads per run and the reads can be easily demultiplexed and analyzed using publicly available software.
Garvan Institute of Medical Research

This work has been related to many disease areas including cancer, neurology, immunology and pathogen identification.
Garvan has performed nanopore sequencing runs related to structural variants and DNA methylation, and done ultra long reads and direct RNA sequencing.
Genome Transcriptome Facility of Bordeaux

- de novo sequencing on bacteria, bacteriophage, fungi, tomato, stevia, oak.
- Amplicon sequencing (15kb long range PCR) for detection of large deletions in human mitochondrial genome.
- 16S analysis of leaf, insect and human microbiote
We look forward to hearing from you
NextOmics, a GrandOmics company
NextOmics, based in China, is providing nanopore sequencing as a service to people across the region, for human, plant, animal and microbial genomics.
GrandOmics, the parent company of NextOmics, has recently launched the Personal Reference Genome Project, which will provide a ‘platinum de novo personal genome’ to customers. The PRGP aims to provide 10K samples in the first 2-3 years and 10 million in the following years.
Read more about the project here: https://www.grandomics.com/PRGSP/
De Novo Genomics

Beyond our sequencing services we have been involved in several research collaborations. A transcription factor project has allowed us to demonstrate the usefulness of nanopore sequencing for ChIP-seq. In some situations we recovered enough material to allow the sequencing of non-amplified libraries. For another project we were assessing the splicing fidelity of transcripts generated from a human disease associated gene. Nanopore sequencing revealed that, for some patients, numerous novel splice isoforms are generated resulting in premature stop codons. One of our more interesting and challenging collaborations has been looking at RNA modifications in reproductive tissue. This collaboration has made us very excited about the use of nanopore sequencing for studying both RNA and DNA base modifications.
We have enjoyed working with researchers to help them leverage Oxford Nanopore sequencing technology from both a service perspective and from more in depth collaborative research projects. Our work has allowed us to develop expertise in a wide range of services that include and are not limited to: whole genome, transcriptome, immunoprecipitation, and target amplicon sequencing. We look forward to continuing our support of researchers in their pursuit of discovery.
Follow us on twitter (@DeNovoGenomics) to get updates on developments or find our contact details via the following link.
Takara Bio Inc.
Takara Bio offers Oxford Nanopore long reads sequence and data analysis services combining our long experience as a sequence service provider.
With advent of next generation sequencing technologies, more organisms including microbes, plants and human are possible to be analyzed and its applications are expanding. We have set up numerous sequencers with high-speed data analysis server accommodating a variety of analysis needs. Oxford Nanopore GridION will help to tackle with non-model organism genome and complex genetics analysis. Our biggest data analysis environment in Japan and long term experienced analysis methods will support your research.
GeneBay

Not only the assembly of small bacterial genomes, but we also see success in assembling larger eukaryotic genomes such as fungi and plants. With these progress, we can now provide high quality de novo assembled genomes using Oxford Nanopore long reads from a variety of organisms such as bacteria, animals and plants.
As a sequencing service provider, we can provide sequencing runs flexible to customers’ specific needs. We can provide sequencing runs favorable to longer read length or higher throughput settings depending on requests. We can accommodate with multiplexing samples in a single flowcell and other analysis as well.
Our long bioinformatics experience will help and guide you to the success of long reads analysis.
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