At Source BioScience, we deliver advanced nanopore sequencing services, providing researchers with the ability to analyse long reads of DNA and RNA in real time. Using Oxford Nanopore Technologies (ONT), we support applications across various sectors, from genomic research to drug development. Our nanopore sequencing technology enables the study of single molecules of DNA, offering high-quality sequence data with comprehensive insights into base modifications and complex genomic structures.
Rapid Turnaround Times
New for 2024:
Delivering unrivalled turnaround times for Whole Plasmid Nanopore Sequencing using our streamlined SpeedREAD™ data delivery system. Providing high-quality data retrieval within 12 hours from sample receipt.
Exclusive offer:
Order whole plasmid nanopore sequencing vouchers and get 25% EXTRA FREE. Limited time only - order now on our portal and use code RAPID25.
Any questions email GSTeam@sourcebioscience.com
A free consultation is available to discover more about the Sequencing services we can offer you.
Contact us in case of any questions.
How To Order
NanoporeAmplicon
15ul @30ng/ÎĽl per sample
Nanopore30
15ul @30ng/ÎĽl per sample
Nanopore150
30ul @30ng/ÎĽl per sample
Nanopore300
50ul @30ng/ÎĽl per sample
Sending Your Samples
Place your samples in a secure package marked with the order number, and either deposit them in your Source Genomics drop box for collection, or use our FREEPOST labels to send your samples to us by post.
Receive Data
Your samples will be processed as soon as they arrive at Source Genomics, and your data will be emailed within 12 hours of sample receipt.
Amplicon
Analyse specific regions of DNA
Nanopore30
For rapid sequencing and assembly of plasmids up to 30kb
Nanopore150
For sequencing and assembly of plasmids/BACs up to 150kb
Nanopore300
For sequencing and assembly of plasmids/BACs up to 300kb
Why Choose Whole Plasmid Nanopore Sequencing?
Long Reads for Comprehensive Analysis
Nanopore sequencing produces long read sequences that capture entire DNA strands, allowing for detailed de novo assembly and improved sequencing performance. This approach is particularly beneficial for projects requiring structural variant detection, such as in human genome research or microbial genome sequencing.
Single-Molecule Real-Time Sequencing
By sequencing single strands of DNA or RNA in real time, nanopore sequencing delivers results quickly and accurately. This method enables direct detection of base modifications without the need for amplification, providing unique advantages for epigenomic studies and single molecule real-time (SMRT) sequencing applications.
Flexibility and High Throughput
Nanopore technology supports the analysis of specific molecules, whether it's DNA sequencing, RNA sequencing, or the integration of multiple samples in a single run. The platform’s high throughput allows for sequencing large genomes, such as the human genome, with robust scalability.
Why Choose Whole Plasmid Nanopore Sequencing?
- Whole Plasmid Sequencing - Enabling entire plasmid constructs analysis for the characterisation of unknown plasmids and the validation of known plasmids
- Whole Genome Sequencing with Epigenome (5mC and 5hmC) - Generate entire human and mammalian genome assemblies with epigenome using long nanopore sequencing reads
- RNA Sequencing - Quantitative isoform expression from bulk or single cell preparations (10X)
- Bacterial Whole Genome Sequencing - Generate microbial genome assemblies with long nanopore sequencing reads
- 16s and Metagenomics - Gain full-length 16S rRNA gene sequencing for taxonomic classification of the genomic material in your sample. Or perform bulk metagenomics to assemble genomes from mixed samples
Sequence DNA And RNA With Increased Efficiency
Using Nanopore Technology, DNA and RNA can be sequenced directly rather than through a copy of a synthetic strand, eliminating the need for an alternative marker. This means that modification information across the genome remains intact and is visible in your data report.
Introducing The Power Of Any Read Length
As a trusted service provider of Nanopore sequencing, Source Genomics provides high-quality long-read sequencing solutions for exceptional genome accessibility. With Nanopore sequencing, fragments from 20bp to millions of bases can be sequenced. The generation of native long-read sequencing data can support all avenues of genomic research, from single tests to ultra-high throughput projects, from cell-free nucleic acid to telomere assemblies.
At Source Genomics, our experienced team will guide you through every step of the process, ensuring your project benefits from the highest level of support and technology. Whether you're conducting large-scale genome studies or focusing on single-strand DNA, our nanopore sequencing services provide the flexibility and precision required for success.
Contact us today and one of our skilled account managers will be in touch with a free consultation including further information and pricing details.