Genome & epigenome
Our Sanger sequencing service is a great way to validate any of your genome-wide discoveries or verify specific sequences in subsets of samples.
We deliver a complete genome sequencing package using our suite of Illumina and Oxford Nanopore Technologies next-generation sequencers. Whether you are sequencing a bacterial, human, or other genome, our experienced team can help you design your project and deliver high-quality data.
Targeted sequencing of regions of the genome allows cost-effective screening of cohorts or populations. We utilise capture products from a range of suppliers so that we can provide you with a design that best fits your project.
We provide a number of different services that utilise next generation sequencing to study epigenetic modifications and their impact on gene regulation. Genome-wide or targeted epigenome services are available.
Provides a wide range of applications from genotyping to methylation profiling using array-based technologies. We have a range of options to suit low- to high-throughput projects to guarantee a fast turnaround time.
The range of genome and epigenome analysis services that we offer is extensive. We're always happy to discuss our various options and guide you towards the best approach for your project.  If there is a technique or technology you are interested in that is not listed on the service menu on the right, contact us as we may be able to offer an alternative solution.
All genomic analyses performed by the Ramaciotti Centre for Genomics are carried out in our ISO/IEC 17025 accredited laboratories.