The South Australian Genomics Centre (SAGC) was established in July 2020 as a state-wide genomics facility to support research in South Australia, as well as nationally and internationally.
The SAGC is a partnership between the South Australian Health and Medical Research Institute, University of South Australia, Flinders University, The University of Adelaide, the Australian Genome Research Facility (AGRF), and the Australian Wine Research Institute (AWRI). Its establishment was supported by an investment of >$7 million, including $2 million from BioPlatforms Australia (BPA).
The SAGC provides a broad range of services including single cell and spatial transcriptomics, RNA sequencing, whole exome and genome sequencing, epigenomics, metagenomics and a range of other custom methods. These services are supported by a dedicated Bioinformatics Platform that supports users of the facility by developing advanced and customised approaches for data analysis, integration and visualisation. All areas of genomics including animal, plant, environmental, microbial, and human genomics are supported.
The South Australian Genomics Centre (SAGC) provides a broad range of services including:
The SAGC offers both Illumina and MGI sequencing. We offer a range of next generation sequencing platforms to find an efficient match for projects of any size. See our range of next generation sequencers with available flow cells and output.
STOmics (SpaTial Enhanced Resolution Omics-Sequencing): whole transcriptomics for discovery applications (range of 1000-2000 genes/cell) leverages in situ mRNA capture and cDNA sequencing with barcoded spatial coordinates to create a spatial transcriptomic profile of the tissue section for analysis.
Xenium Analyser allows targeted gene expression and protein quantification at subcellular resolution. Xenium is an end-to-end platform that enables high-throughput subcellular mapping of RNA targets.
VisiumHD Spatial Transcriptomics allows whole transcriptome mapping within morphological context of complex tissue samples. There is no need to select targets or specific region of interest. Compatible with FFPE and is CytAssist enabled which allows transfer of archived tissue slides to the special barcoded Visium slides to both improve workflow and reduce RNA diffusion.
Genomics SAGC has a Chromium Controller and Chromium X Series from 10X Genomics to enable multiomic analysis through droplet GEM-based single cell partitioning and sequencing.
Applications available:
*Cell surface marker tagging can be incorporated into some of these techniques and quantified during sequencing.
Compatible with fixed, fresh, and frozen samples, as well as whole cells and nuclei.
Evercode is a plate-based combinatorial barcoding technology that enables very large single cell experiments (up to 1 M cells or 96 samples) in a single workflow with either fixed or fresh cells. This approach can offer some advantages with certain cell types and achieve higher throughput at a lower cost compared to microfluidic based approaches.
SAGC Flinders Node Facility Manager: Benjamin.Mayne@sahmri.com
Bioinformatics: Daniel.Thomson@sahmri.com
The SAGC Flinders Node is located at the Flinders Centre for Innovation in Cancer (FCIC) at Flinders Medical Centre, Flinders Drive, Bedford Park SA 5042 (Room 4L160)
Sturt Rd, Bedford Park
South Australia 5042
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