Services

We have offer a wide range of kits for bespoke analysis of your sample.

We can offer an in house service where you can drop your samples off for analysis or we can train you to competency so you can perform analysis yourself.

Download request form

Enquire here

We are experienced in a wide range of library production techniques allowing you access to the most up to date methods in your field.

• Resequencing and De novo Sequencing
• Amplicon sequencing
• Exome or Targeted Sequencing to analyse protein-coding regions of the genome
• ChiP Seq ( library prep only)
• Methylome sequencing to understand how modification can affect gene regulation
• Targeted Sequencing to produce in-depth views of genetic variation for phylogenetic studies (16S rRNA, 18S rRNA, ITS etc)
• Whole Transcriptome Analysis to gain a comprehensive view of total RNA and non-coding RNA (RNA-Seq, Small RNA-Seq, Stranded RNA-Seq)
• Single cell sequencing

We are able to offer a range of standard library preparation, but are also willing to help you create your own. Whether you require help troubleshooting, tips on best practice, we are prepared to help.

Library preparations offered in house. Click here for more information

Download request form

Enquire here

Single cell genomics is the cutting edge of genomics capabilities. We can support you through the entire process, from initial project scoping and design, platform selection, sample preparation and processing.

With access to the Genomics 10X Chromium Controller and the Fluidigm C1 single-cell auto-prep system individual cells can be isolated with precision and libraries amplified for sequencing. 

Download request form

Enquire here

The Genomics CTU have 3 Illumina next generation sequencers; MiSeq personal sequencer, NextSeq 500, NovaSeq 600

The MiSeq is an integrated bench top sequencer. It features significantly faster cycle times allowing small projects to be completed quickly at a lower cost.

The‌ MiSeq delivers high precision variant detection and is suitable for small-scale projects such as amplicon or small genome sequencing. ‌It typically sequences more than 20 million inserts per lane from a sequencing run.

The NextSeq 550 allows researchers to perform many combinations of high- and mid-throughput sequencing applications. Researchers can carry out applications such as whole genome sequencing, exome sequencing, whole transcriptome sequencing, mRNA-Seq, and methylation sequencing, among others. It typically sequences more than 400 million inserts per lane from a sequencing run.

With The NovaSeq 6000 Sequencing System you can get scalable throughput and flexibility for virtually any sequencing method, genome, and scale of project. The NovaSeq 6000 System offers output up to 6 Tb and 20 B reads in < 2 days. Multiple flow cell types and read length combinations offer flexible output and run time configurations based on project needs (Table 1). NovaSeq S Prime (SP), S1, and S2 flow cells provide quick and powerful sequencing for most high-throughput applications. With fewer reads than a HiSeq 2500 or HiSeq 4000 flow cell and the flexibility of individual lane loading, the NovaSeq SP and S1 flow cells allows existing HiSeq System users to transition easily, without the need to batch additional samples per run. (Comparison reads for the HiSeq 2500 System based on specifications for the v4 high output flow cell.) The NovaSeq S4 flow cell enables high-throughput cost-effective sequencing across a range of applications, making in-house WGS or WES studies an attractive and affordable option for more labs.

Click here for further information.

Download request form

Enquire here

The GCTU operates an ABI3730 capillary sequencing instrument, and offer a range of sequencing services. These include;

Sequencing

Researchers can deliver samples that have already been sequenced with BigDye reagents. We can perform clean-up and capillary analysis on the ABI3730, or the researcher can deliver clean DNA and sequencing primer. We will perform the BigDye sequencing, clean-up and capillary analysis on the ABI3730.

Genotyping with microsatellites

We also provide a range of fragment analysis options to customers and are happy to assist customers with their data analysis needs as well. Fragment Analysis is a type of genetic marker analysis, is a technique that facilitates identifying the presence or absence of a DNA sequence that is linked to an allele of interest. It does not provide the sequence information of a particular gene; instead changes in the length of specific DNA sequences provide key information to distinguish changes in markers.

We can analyse your PCR-amplified microsatellite or AFLP samples on the ABI3730 instrument. We can either return the data to you, or assist by giving you access to GeneMapper tools. 

Genomics CTU also offer STR profiling of cell lines

Click here for more information on prices.

Download request form

Enquire here

The main objective is to establish a GCTU reputed for technical advice and support for researchers around NGS capabilities.

The GCTU strives to support research groups by delivering advice, and training for as many internal research grant applications considering NGS workflows. 

The GCTU manager along with the academic leads have years of experience in arranging collaborations and coordinating NGS research. From this an Expert Users Working Group (EUWG) has been created and convenes to cement provisions for development and for supplying experimental design and collaborations, as well as supporting grant writing, aiding the principal researcher with hypothesis.

Inline with this the GCTU offers training for students who wish to develop their NGS knowledge and skill set. Researchers will be trained to competency standards adhered to within the GCTU and will offer the opportunity for those trained to be embedded within the GCTU.

Enquire here