Source Genomics is a high-quality, UK-based service provider of Oxford Nanopore Technologies (ONT) for rapid, long-read, real-time sequencing of whole plasmid DNA with data delivery within 12 hours from sample receipt utilising Source Genomics extensive dropbox network.
Rapid Turnaround Times
New for 2024:
Delivering unrivalled turnaround times for Whole Plasmid Nanopore Sequencing using our streamlined SpeedREADβ’ 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
Unrivalled Data Quality
Rapid Turnaround Times
Scalable
Global Provider From ISO-accredited Laboratories
Source BioScience is a Certified Service Provider for Oxford Nanopore Technologies on the GridION and P2 Solo devices. View the certificate.
A free consultation is available to discover more about the Sequencing services we can offer you.
Contact us in case of any questions.
Whole Plasmid Nanopore Sequencing
Whole plasmid sequencing involves the thorough examination and analysis of the entire genetic code of a plasmid, referred to as plasmid DNA (pDNA).
Our Nanopore whole plasmid sequencing service offers in-depth insights into the genetic composition of plasmids and their potential applications in gene knockout and editing studies. Whole Plasmid sequencing enables the extraction of valuable genomic data, contributing to enhanced comprehension of microbial diversity, evolution, and the intricate mechanisms that govern biological processes.
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
Amplicon Sequencing
Amplicon sequencing is a powerful technique that involves the amplification of target DNA sequences using polymerase chain reaction (PCR), followed by high-throughput sequencing to determine the sequence of the amplified DNA fragments. This method allows researchers to quickly and efficiently analyse specific regions of DNA from a complex mixture of genetic material, making it an invaluable tool in genomics research and various applications in science and medicine.
Contact us today and one of our skilled account managers will be in touch with a free consultation including further information and pricing details.